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The longitudinal trajectory of CSF sTREM2: the alzheimer’s disease neuroimaging initiative

Alzheimer's Research & Therapy volume 16, Article number: 138 (2024) Cite this article

Abstract

Background

The soluble triggering receptor expressed on myeloid cells 2 (sTREM2) in cerebrospinal fluid (CSF) is considered a biomarker of microglia activity. The objective of this study was to investigate the trajectory of CSF sTREM2 levels over time and examine its association with sex.

Methods

A total of 1,017 participants from the Alzheimer’s Disease Neuroimaging Initiative Study (ADNI) with at least one CSF sTREM2 record were included. The trajectory of CSF sTREM2 was analyzed using a growth curve model. The association between CSF sTREM2 levels and sex was assessed using linear mixed-effect models.

Results

CSF sTREM2 levels were increased with age over time (P < 0.0001). No significant sex difference was observed in sTREM2 levels across the entire sample; however, among the APOE ε4 allele carriers, women exhibited significantly higher sTREM2 levels than men (β = 0.146, P = 0.002).

Conclusion

Our findings highlight the association between CSF sTREM2 levels and age-related increments, underscoring the potential influence of aging on sTREM2 dynamics. Furthermore, our observations indicate a noteworthy association between sex and CSF sTREM2 levels, particularly in individuals carrying the APOE ε4 allele.

Introduction

The triggering receptor expressed on myeloid cell 2 (TREM2) is exclusively expressed by microglia in the brain [1]. As a transmembrane receptor, TREM2 mediates protective functions on microglia, serving as a regulator of phagocytosis and suppression of inflammatory reactivity [2, 3]. Further, TREM2 mutations are known to be a risk factor for sporadic Alzheimer’s disease (AD) [4]. TREM2 extracellular domain is capable of binding various ligands related to microglia, such as lipopolysaccharides (LPS), phospholipids, high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), ApoE, apoptotic neurons, and soluble amyloid-beta (Aβ) [5]. A soluble form of TREM2 (sTREM2) is generated through cleaving the TREM2 extracellular domain by ADAMs (a disintegrin and metalloproteinase) after ligand binding [6]. Although cerebrospinal fluid (CSF) sTREM2 is considered a biomarker of microglia activity [7, 8], the biological role of sTREM2 in AD is poorly understood [9,10,11]. Previous studies suggested that sTREM2 could exert neuroprotective effects by enhancing the clearance effect of microglia for Aβ plaque in earlier stages of dementia [12, 13]. However, it is unclear whether microglia can efficiently regulate Aβ levels, because microglia in a morphologically dystrophic state with loss of surveillance function have been found in late-stage AD, leading to reduced Aβ clearance in late-onset AD patients [14].

Age, sex, and APOE ε4 status are major risk factors for dementia, and previous studies examined their relationships with CSF sTREM2 levels [15,16,17,18]. These studies suggested aging was associated with sTREM2, the sex differences were inconclusive. While APOE ε4 could change the structure of TREM2 and influence TREM2 mRNA expression, its association with sTREM2 levels was not significant [19, 20]. Notably, elevations in sTREM2 levels have been observed in AD, but the highest sTREM2 levels were found during the early phase of AD [15, 18, 21]. A few studies utilizing the ATN profiles have depicted sTREM2 in contrast to amyloid and tau aggregating [9]. These potential changes of sTREM2 over cognitive impairment might be attributed to that microglia function and density exhibit considerable population and spatial heterogeneity in the brain [22, 23]. However, few previous studies have specifically investigated the trajectory of CSF sTREM2 levels over time [17]. Studying the longitudinal dynamic trajectories of sTREM2 can have significant implications for understanding the biological processes underlying neurodegenerative diseases, particularly those involving microglial activation and neuroinflammation [24]. Further, it has the potential to deepen our understanding of AD, uncover novel therapeutic targets, and pave the way for precision medicine approaches tailored to individual trajectories [25,26,27]. Thus, it is necessary to clearly describe the trajectory of sTREM2 over time to understand better the biological implications of CSF sTREM2 levels.

To this end, we aimed to investigate the trajectories of CSF sTREM2 and to examine the association of CSF sTREM2 with sex using a large longitudinal cohort.

Methods

Study population

Participants were selected from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) study, which consisted of 1,031 participants who had CSF sTREM2 measured. The ADNI cohort is a multi-site longitudinal study that began in 2004 to validate biomarkers in dementia or AD clinical trials. A total of 4,139 participants were recruited with follow-up assessments performed every six months in the US and Canada between 2004 and 2021. During the follow-up visits, demographic information, cognitive assessments, and biomarker records were obtained within a six-month time window. More detail about the ADNI study design and the participant recruitment procedure has been described elsewhere [28]. The individuals from ADNI cohort with at least one CSF sTREM2 record were included. Figure S1 presents the selection process for the analytical sample and data used from the ADNI cohort. The final study sample for the present study comprised 1,017 participants, including 305 CN individuals, 519 with MCI, and 193 with dementia at baseline. Participants in MCI or dementia subgroups were older and more likely to be men. At the baseline, the CSF sTREM2 had a median value of 3,598 (interquartile range: 2,490, 5,174) pg/ml. During the follow-up period, 404 participants had sTREM2 measured twice and over. Detailed characteristics of the study participants are described in Table S1.

Measurement of CSF sTREM2 and other biomarkers

The levels of CSF sTREM2 were measured by a sandwich-based ELISA approach using the mesoscale discovery (MSD) platform, which had been elaborated and validated previously [29]. For the measurements of CSF sTREM2, a subset of the samples from the same participants were measured separately in the Piccio group and Haass group. The ADNI biomarker core flagged 25 individuals, who were outside of the 98% prediction tolerance levels that was constructed by predicting the linear regression model between the two measurements. According to their suggestion, we removed these 25 individuals in subsequent analyses, and MSD sTREM2corrected was utilized for the following statistical analyses [30].

The levels of β-amyloid (1–42) (Aβ1−42), total tau (t-Tau), and phosphotau (181P) (p-Tau) in CSF by the ADNI Biomarker Core were measured using the Elecsys β-amyloid (1–42) (Roche Diagnostics) CSF, the Elecsys Total-Tau CSF, and the Elecsys phosphotau (181P) CSF immunoassays, respectively [31].

Classification of cognitive status

Clinical cognitive status was classified by ADNI investigators as follows: normal cognitive (CN: Mini-Mental State Examination [MMSE] ≥ 24, Clinical Dementia Rating [CDR] = 0, and non-depressed), mild cognitive impairment (MCI: MMSE ≥ 24, CDR = 0.5, objective memory-impairment on education-adjusted Wechsler Memory Scale II, and preserved activities of daily living) or dementia (MMSE = 20–26, CDR ≥ 0.5, and NINCDS/ADRDA criteria for probable AD). Following the 2018 NIA-AA criteria, each ADNI participant was assigned into groups by the ATN framework. In the present study, the ATN biomarker profiles include three biomarkers: “A” as Aβ aggregation, “T” as tauopathy, and “N” as neurodegeneration. Aβ-positive (A+) participants were those with CSF Aβ1−42 levels < 976.6 pg/ml. Tau-positive (T+) participants referred to those with p-tau > 21.8 pg/ml. Neurodegenerative-positive (N+) participants were those with t-tau > 245 pg/ml [32]. Given CSF p-Tau181P and CSF t-Tau are highly correlated, the “T” (tau pathology) and “N” (neurodegeneration) groups were merged [30]. The TN- was defined as both the normal range of aggregated tau and neurodegeneration. The TN + presented those with tau pathology or neurodegeneration.

Covariates

The covariates included in the analyses were selected based on various factors previously reported to be associated with CSF sTREM2, inflammation in the brain, as well as imbalanced demographic characteristics comparing the recruited study sample to the ADNI entire sample. These included age, sex, race/ethnicity, TREM2 rare variant carrying status, APOE ε4 allele, educational attainment, smoking, marital status, clinical cognitive status, and AD core biomarkers. Race/ethnicity was classified as non-Hispanic white and others (non-Hispanic black, non-Hispanic others, and Hispanic). According to APOE ε4 allele status, participants were classified as APOE ε4 non-carrier (APOE ε2/ε2 or APOE ε2/ε3 or APOE ε3/ε2 or APOE ε3/ε3), APOE ε4 heterozygote (APOE ε3/ε4 or APOE ε2/ε4), APOE ε4 homozygote (APOE ε4/ε4). Participants were stratified into non-smokers if they reported no history of cigarette smoking and as smokers if they reported a history of cigarette smoking. Marital status was classified as either married or others (widowed, divorced, never married, and unknown).

Statistical analysis

The distributions of demographic characteristics and biomarkers levels at baseline among three cognitive status groups (CN, MCI, and dementia) were compared by Pearson chi-square test for categorical variables, one-way analyses of covariance (ANCOVA) for continuous variables, and Mann-Whitney U test for ordinal categorical variables. To allow for interpretation on a relative scale and to account for non-normal distribution, levels of CSF sTREM2, CSF Aβ1−42, CSF t-Tau, and CSF p-Tau underwent loge transformation.

Linear mixed-effect models were employed to fit growth curves to the repeated measurements of CSF sTREM2. In these models, each trajectory parameter (intercept and slope) was allowed to vary from individual to individual (as random effects) and to vary by the trajectory, baseline demography, and cognitive impairment factors for each participant (as fixed effects). To give the coefficients a meaningful interpretation at zero, and to avoid multicollinearity, variables were centered in the models. Covariates were added in a stepwise fashion into a series of models. Model 1 included age as fixed effects with an additional random slope and intercept for age. Model 2 added sex as covariate. Model 3 further added race/ethnicity, TREM2 rare variant carrying status, APOE ε4 carrying status (fixed effects). Model 4 additionally adjusted educational attainment, smoking status, marital status, and clinical cognitive status. Model 5 and model 6 additionally controlled for CSF Aβ1−42, CSF t-Tau, CSF p-Tau, and the p-Tau/Aβ1−42 ratio. The goodness of fit of the model was evaluated with Akaike’s information criteria (AIC). Finally, interaction analyses and ANCOVA analyses were conducted to test for longitudinal interaction effects between age, sex, and each covariate to determine whether CSF sTREM2 trajectories varied according to specific demographic and other factors. The primary codes for the model implementation have been provided in the Supplementary files.

All statistical analyses were performed using R 4.2.2. All tests were 2-tailed, with a significance level of α = 0.05.

Results

Distribution of CSF sTREM2 at baseline

Figure 1A illustrates that baseline levels of CSF sTREM2 were significantly associated with age (β = 77.26, P < 0.001, Table 1). Specifically, the yearly increment in CSF sTREM2 was 82 pg/ml for those aged 55–64 years and 33 pg/ml for those aged 65–74 years. CSF sTREM2 dramatically increased for individuals over 75 years old (Pinteraction=0.023), with an average annual rise of 133 pg/ml. In addition, mean CSF sTREM2 concentrations were significantly higher in A-T + group (A-T+, 5302 pg/ml > A + T+, 4284 pg/ml > A-T-, 3555 pg/ml > A + T-, 2809 pg/ml, Figure S2A) and non-Hispanic whites (4129 pg/ml vs. 3174 pg/ml, P < 0.001, Figure S2B) than others, whereas CSF sTREM2 levels did not vary substantially by sex, clinical cognitive status, or APOE ε4 carrier status (Fig. 1B, Figure S2C, Figure S2D).

Fig. 1
figure 1

(A) The dynamic change of CSF sTREM2 over age among CN, MCI, and dementia groups at baseline. Solid lines represent the regression lines for the three clinical cognitive performance subgroups: the green line and points denote the cognitively normal group, the orange line and points denote the MCI group, and the red line and points denote the dementia group. (B) The distribution of CSF sTREM2 levels by sex at baseline. Abbreviations CN, cognitively normal controls; MCI, mild cognitive impairment

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The longitudinal trajectory of CSF sTREM2 over time

The longitudinal trajectories of CSF sTREM2 levels using cubic spline models by clinical cognitive status were displayed in Fig. 2A. The increasing trends of these trajectories exhibited slight variations among CN, MCI, and dementia groups. Notably, above the age of 75, we did not detect a significantly faster growth rate in longitudinal sTREM2 levels (Pinteraction=0.389, Table 1; Fig. 2B). Furthermore, the observed slight differences in sTREM2 trajectories among patients with MCI or dementia were not statistically significant compared with cognitively normal individuals (β=-0.005, P = 0.299; β=-0.006, P = 0.305, Table S2).

Fig. 2
figure 2

(A) Longitudinal trajectories of CSF sTREM2 over time among CN, MCI, and dementia groups. Thin solid lines connecting points indicate changes in CSF sTREM2 of follow-up for each individual. Thick solid lines represent the trajectories of CSF sTREM2 using cubic spline models for three clinical cognitive performance subgroups at baseline: the green lines signify the cognitively normal group, the orange lines signify the MCI group, and the red lines signify the dementia group. (B) The correlation coefficients between age and CSF sTREM2 among different age ranges. The regression coefficients and confidence intervals were obtained using linear mixed-effect models, without adjusting for covariates. Abbreviations CN, cognitively normal controls; MCI, mild cognitive impairment; CI, confidence interval

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Table 1 Annual change rates of CSF sTREM2 by baseline age interval and consecutive slope difference using baseline and longitudinal data, ADNI cohort, United States and Canada, 2004–2021
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The longitudinal association of CSF sTREM2 with age

The overall results of fixed-effect models showed a strong positive association between age and CSF sTREM2 (P < 0.0001, Table 2). The average annual change of sTREM2 was 2.2% (the average rate increase was 90 pg/ml per year), controlling for sex, race/ethnicity, TREM2 rare variant status, APOE ε4 allele status, educational attainment, smoking, marital status, and clinical cognitive status in model 4 (Table 2). This finding remained consistent after controlling for CSF Aβ1−42, CSF t-Tau, CSF p-Tau, and p-Tau/Aβ1−42 ratio (model 5, model 6). Moreover, A + T- group exhibited faster age-related increase in sTREM2 levels than others (Table 3; Fig. 3A).

Fig. 3
figure 3

(A) Longitudinal interaction between the ATN profiles and age in CSF sTREM2 levels. This figure illustrates the interaction effect of ATN profiles on longitudinal age-related changes in CSF sTREM2 within a mixed-effect model considering covariates, using the ‘interact_plot’ function from the ‘interaction’ package. Red points represent the A + T- group, and green points represent the other groups (A-T-, A-T+, A + T+). Regression lines are shown for the A + T- group (red, solid) and the other groups (green, dashed), with standard errors represented by red and green shading. (B) Longitudinal interaction between APOE ε4 and sex in CSF sTREM2 levels. This figure illustrates the interaction effect of APOE ε4 on longitudinal sex-related changes in CSF sTREM2 within a mixed-effect model considering covariates, using the ‘cat_plot’ function from the ‘interaction’ package. Red points represent the female group, and green points represent the male group

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Table 2 Longitudinal trajectory of CSF sTREM2 and the association of CSF sTREM2 with sex using longitudinal data, ADNI cohort, United States and Canada, 2004–2021
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The longitudinal association of CSF sTREM2 with sex

Compared with men, women did not have significantly higher levels of CSF sTREM2 controlling for age (β = 0.013, P = 0.683, Table 2), and the difference remained nonsignificant after further adjusting for race/ethnicity, TREM2 rare variant status, APOE ε4 allele status, educational attainment, smoking, marital status, and clinical cognitive status (β = 0.043, P = 0.203). Nevertheless, the interaction effects between APOE ε4 and sex, as well as between educational attainment and sex, were pronounced in model 4 (β = 0.159, P = 0.016; β = 0.207, P = 0.049, Table 3; Fig. 3B). In subgroup analysis stratified by APOE ε4 carrying status, a significant increase in sTREM2 levels was observed in women compared to men among APOE ε4 carriers (β = 0.146, P = 0.002, Table S3). In an exploratory stratified analysis by sex, females carrying the APOE ε4 allele, as well as those with higher educational attainment, exhibited significantly higher sTREM2 levels after covariate adjustment (β = 0.104, P = 0.036; β = 0.021, P = 0.019, Table S3).

Table 3 Interaction effect analysis of age and covariates, sex and covariates in CSF sTREM2 using longitudinal data, ADNI cohort, United States and Canada, 2004–2021
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Discussion

In the present study, our prospective analysis of 1,017 individuals from the ADNI cohort demonstrated the longitudinal trajectories of CSF sTREM2 levels. CSF sTREM2 levels were increased over age, and strong positive linear correlations were seen among CN, MCI, and dementia groups. While the trajectories of sTREM2 did not show significant variation across the three clinical cognitive groups, there was a notably faster rate of increase in sTREM2 levels following the onset of amyloid pathology in the early stages of AD. Furthermore, women exhibited significantly higher sTREM2 levels compared to men among the APOE ε4 allele carriers, but this sex difference was not significant across the entire sample.

A few cross-sectional studies have reported a strong positive association between age and CSF sTREM2 [16,17,18, 33,34,35]. Moreover, this association has also been observed in several cohorts of Parkinson’s disease [36, 37]. Further, in a hospital-based longitudinal study of Swedish and Norwegian participants, Henjum et al. found that CSF sTREM2 levels were related to age only in cognitively normal participants, not in those with MCI or AD [17]. In contrast, elevated levels of sTREM2 with age were reported for CN, MCI, and dementia participants in a pooled study with five memory clinics, which are consistent with our results [15]. Around 75% of sTREM2 is generated by the shedding of full-length TREM2 [38]. An age-related increase in TREM2 mRNA expression was demonstrated in previous transcriptome analyses in both elderly AD mouse models [39] and human AD brains [19, 40, 41]. Therefore, CSF sTREM2 elevated with aging would mainly be attributed to TREM2 expression.

Regarding the sTREM2 trajectory, in contrast to the results of Suárez-Calvet et al., our study did not observe a faster increase in sTREM2 levels among individuals with MCI or dementia compared to cognitively normal individuals [42]. This divergence in findings might be attributed to the different age ranges of the study samples (40–100 years vs. 54–94 years). In ATN profiles, although the individuals with Aβ pathology without tau pathology or neurodegeneration (A + T-) at baseline exhibited lower sTREM2 levels compared to other stages, a more rapid increase rate in sTREM2 was observed in those with this initial Aβ pathology stage during follow-up. This is consistent with findings from the Dominantly Inherited Alzheimer Network (DIAN) study, in which Morenas-Rodríguez et al. reported that a high baseline amyloid burden was a predictor of the annual increase rates of sTREM2 in carriers of pathogenic variants (APP/PSEN1/PSEN2). These observations indicated there might be an accelerated increase in sTREM2 in the early stages of AD [43]. One possible explanation is that the inflammatory response to Aβ deposition within the brain might trigger higher amounts of tau to be released into CSF, thereby further influencing microglia reactivity processes and subsequent neurodegeneration [21, 44].

In our dataset, the trajectories of sTREM2 demonstrated a notable acceleration after the age of 75, particularly within the cognitively normal subgroup. This pattern of change is consistent with observations of age-related proteins in plasma, which have shown similar acceleration at critical ages (34, 60, and 78) in the aging process, implicating blood pathways and bone morphogenetic protein signaling [45]. The observed increase in CSF sTREM2 levels after the age of 75 may be attributed to factors such as race, ethnicity, or varying levels of tau dynamic change in the CSF [46]. Our study sample exhibited a higher proportion of non-Hispanic whites in the 80–94 age group, followed by the 75–79 and 70–74 age groups. Additionally, a slight acceleration in the growth rate of t-Tau was observed after the age of 75 (with increases of 5.78, 6.14, and 6.32 pg/ml per year in the age groups of 70–74, 75–79, and 80–94, respectively). Furthermore, it has been documented that inflammatory stimuli predominantly increase TREM2 expression in vivo [47]. Various basal pro-inflammatory cytokines exhibit nonlinear trajectories, with specific acceleration inflection points, such as IL-6 and IL-10 in plasma at approximately the age of 70 [48,49,50], and YKL-40 in CSF around 60 years old [51]. These findings collectively suggest that inflammation and microglial dysfunction may accelerate in older individuals.

A previous study reported a significantly higher sTREM2 in men (n = 106) compared to women (n = 112) in DIAN [52], similar to another study based on Alzheimer’s Disease Research Center (ADRC) cohort (P = 0.017) [18]. However, a recent European study found that CSF sTREM2 levels were not associated with sex (P = 0.179) [42]. Results from the Chinese Alzheimer’s Biomarker and Lifestyle (CABLE) study also found that sTREM2 concentration was not affected by sex (P = 0.576) [16]. In Parkinson’s disease, inconsistent results were found regarding CSF sTREM2 and sex. While Parkinson’s Progression Markers Initiative data reported no association (P = 0.888) [37], the Pacific Udall Center Cohort revealed significantly higher sTREM2 levels in men than in women (P < 0.0001) [36]. The inconsistent findings from different cohorts were partly due to the different sample sizes examined. A possible explanation would be that there is a differential neuroinflammatory response to p-Tau accumulation between men and women [53, 54], and that late-life changes in estrogen levels among women have a direct effect on tau [55, 56]. Studies with larger samples are needed to further examine this association.

Exploratory stratified analysis by sex showed that women carrying the APOE ε4 allele had higher CSF sTREM2 levels, but this pattern was not observed in men. These results were consistent with previous studies demonstrating an interaction between APOE ε4 allele and sex [57, 58]. Wood et al. discovered that the APOE ε2 allele selectively protected men against cognitive decline compared to the APOE ε3/ε3 but was not as protective in women [59]. In a previous examination of the ADNI cohort, a significant disparity was observed in brain hypometabolism and cortical thinning among female APOE ε4 carriers, who exhibited more profound effects compared to female non-carriers [60]. Several studies have consistently reported an APOE ε4-dependent sex difference in the deposition of p-Tau and t-Tau [61,62,63,64]. Wang et al. further expanded on this finding, revealing that APOE ε4 carriers in females displayed significantly higher tau burden in specific brain regions, including the hippocampus, entorhinal cortex, and parahippocampal cortex, compared to APOE ε4 carriers in males. Notably, the authors also identified a positive correlation between microglial activity and the escalation of amyloid load, particularly among female APOE ε4 carriers [65]. This association further underscores the complexity of the APOE ε4-sex interaction in the pathogenesis of AD. Underlying mechanisms could be that estrogen following menopause promoted the release of APOE from microglia [66], enhancing the APOE ε4 effect on Aβ [67], thereby further stimulating microglia activity [65]. Another possibility is that the interaction between APOE ε4 genotype and sex might directly affect the microglial activity in the brain and could accelerate the risk of AD [68]. In addition, our results also showed that the association between educational attainment and CSF sTREM2 was only significant in females. This is in line with previous research which demonstrated that cognitive reserve may protect against amyloid-related cognitive impairment [69,70,71]. The sex differences in neuroprotective effects of cognitive reserve may be related to CSF sTREM2 [72, 73].

Our analysis did not yield significant differences in sTREM2 levels between the cognitively normal group and the Alzheimer’s disease or mild cognitive impairment groups. This observation could be biological plausibility, given the varying severity of cognitive impairment across different cohorts. In our study, the majority of AD cases exhibited very mild MMSE scores (23 ± 2) [21] and it is noteworthy that MMSE scores in AD patients have been correlated with levels of microglial activation [74]. Furthermore, the levels of aberrant microglial activation are influenced not only by clinical cognitive status or neuroinflammation [75], but also directly affected by the status of Aβ and tau [76]. Within the ATN profiles of our study population, 89% of AD patients exhibited abnormal Aβ pathology, while 32% and 40% of the CN group displayed abnormal Aβ or tau pathology, respectively. It is worth noting that during the follow-up period, the dementia group demonstrated higher sTREM2 levels than the cognitively normal group, although this difference did not reach a significant level after adjusting for age. This finding is consistent with previous analyses [15, 26], underscoring the potential significance of age as a key factor in understanding the function and status of sTREM2.

Our study has several strengths that address the methodological shortcomings of earlier studies. An important strength of this study was the relatively large population-based cohort with repeated measurements of sTREM2 and its comprehensive record of the demographic characteristics, assessment of dementia, and detailed measurement of CSF sTREM2, Aβ1−42, and t-Tau level. The rich information on the participants allowed us to consider more comprehensively covariates and obtain a more thorough understanding of various aspects associated with CSF sTREM2. Furthermore, the record involved the measurement date of sTREM2 and date of birth, which enabled us to employ longitudinal data and mixed-effect models. The mixed-effect model had the advantage of being able to add more covariates that may have collinearity but are essential since most predictive variables had been centered before being added to models. Importantly, given the substantial inter-individual variability in sTREM2 levels [77, 78], the longitudinal study design provides an opportunity to accurately explore the relationships between sTREM2 and age, sex, as well as to compare differences in trajectories of CSF sTREM2 across different clinical cognitive status.

Our study also has limitations. ADNI cohort did not provide inclusion and exclusion criteria for the participants that measured CSF sTREM2. Thus, it is difficult to interpret the distribution of clinical cognitive status in the study sample. For example, there were more MCI participants than CN participants at baseline. Therefore, we cannot rule out the possibility that selection bias influenced our results. In the current study, conclusions pertaining to microglial activity based on sTREM2 measurements must be approached with caution. The sTREM2 assay employed in the ADNI cohort quantified total sTREM2 levels in the cerebrospinal fluid, which comprises both directly transcribed sTREM2 from sTREM2 mRNA and sTREM2 derived from TREM2 shedding [43]. Notably, approximately 25% of the total sTREM2 quantified originates directly from transcription, rather than via TREM2 shedding, thereby reducing the specificity of the measured sTREM2 as a sole indicator of microglial activity [38]. Moreover, sTREM2 itself possesses distinct functional roles, such as preventing the aggregation of Aβ and promoting microglial phagocytosis of Aβ [13, 79]. While interpreting the results, it is important to acknowledge the limitation of skewed ethnic representation within our cohort. The considerable discrepancy between the Non-white Hispanic subgroup and other ethnicities, raises potential concerns regarding the generalizability of our findings. This disparity underscores the need for caution when extrapolating the study outcomes to populations with diverse ethnic backgrounds [46, 80, 81]. Finally, although mixed-effect models were used to analyze this longitudinal data, the number of follow-up visits was small.

Conclusions

In conclusion, our findings highlight the association between CSF sTREM2 levels and age-related increments, underscoring the potential influence of aging on sTREM2 dynamics. Furthermore, our observations indicate a noteworthy association between sex and CSF sTREM2 levels, particularly in individuals carrying the APOE ε4 allele. These findings emphasize the importance of considering sex-specific differences in sTREM2 levels, especially in the context of genetic risk factors for neurodegenerative diseases. Further research into the interplay between sex, genetic factors, and sTREM2 dynamics is warranted to elucidate the underlying mechanisms and potential implications for disease progression and therapeutic interventions.

Data availability

No datasets were generated or analysed during the current study.

Abbreviations

sTREM2:

Soluble triggering receptor expressed on myeloid cells 2

CSF:

Cerebrospinal fluid; ADNI: the Alzheimer’s Disease Neuroimaging Initiative Study

AD:

Alzheimer’s disease

LPS:

Lipopolysaccharides

HDL-C:

High-density lipoprotein cholesterol

ApoE:

Apolipoprotein E

LDL-C:

Low-density lipoprotein cholesterol

Aβ1−42 :

β-amyloid (1–42)

t-Tau:

Total tau

p-Tau:

Phosphotau (181P)

MMSE:

Mini-Mental State Examination

CDR:

Clinical Dementia Rating

NINCDS:

National Institute of Neurological and Communicative Disorders

ADRDA:

Stroke and the Alzheimer’s Disease and Related Disorders Association

CN:

Normal cognitive

MCI:

Mild cognitive impairment

ANCOVA:

One-way analyses of covariance

AIC:

The Akaike information criterion

DIAN:

Dominantly Inherited Alzheimer Network

ADRC:

Alzheimer’s Disease Research Center

CABLE:

The Chinese Alzheimer’s Biomarker and Lifestyle

References

  1. Zhao N, Qiao W, Li F, Ren Y, Zheng J, Martens YA, et al. Elevating microglia TREM2 reduces amyloid seeding and suppresses disease-associated microglia. J Exp Med. 2022;219:e20212479.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Kleinberger G, Yamanishi Y, Suárez-Calvet M, Czirr E, Lohmann E, Cuyvers E et al. TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis. Sci Transl Med. 2014;6.

  3. Raha AA, Henderson JW, Stott SRW, Vuono R, Foscarin S, Friedland RP, et al. Neuroprotective effect of TREM-2 in aging and Alzheimer’s Disease Model. JAD. 2016;55:199–217.

    Article  Google Scholar 

  4. Park S-H, Lee E-H, Kim H-J, Jo S, Lee S, Seo SW, et al. The relationship of soluble TREM2 to other biomarkers of sporadic Alzheimer’s disease. Sci Rep. 2021;11:13050.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Colonna M. The biology of TREM receptors. Nat Rev Immunol. 2023;23:580–94.

    Article  CAS  PubMed  Google Scholar 

  6. Ulland TK, Colonna M. TREM2 — a key player in microglial biology and Alzheimer disease. Nat Rev Neurol. 2018;14:667–75.

    Article  CAS  PubMed  Google Scholar 

  7. Teipel S, Bruno D, Plaska CR, Heslegrave A, Ramos-Cejudo J, Osorio RS, et al. Association of CSF sTREM2, a marker of microglia activation, with cholinergic basal forebrain volume in major depressive disorder. J Affect Disord. 2021;293:429–34.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Paolicelli RC, Sierra A, Stevens B, Tremblay M-E, Aguzzi A, Ajami B, et al. Microglia states and nomenclature: a field at its crossroads. Neuron. 2022;110:3458–83.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Brown GC, St George-Hyslop P. Does Soluble TREM2 protect against Alzheimer’s Disease? Front Aging Neurosci. 2021;13:834697.

    Article  CAS  PubMed  Google Scholar 

  10. Filipello F, Goldsbury C, You SF, Locca A, Karch CM, Piccio L. Soluble TREM2: innocent bystander or active player in neurological diseases? Neurobiol Dis. 2022;165:105630.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Schindler SE, Holtzman DM. CSF sTREM2: marking the tipping point between preclinical AD and dementia? EMBO Mol Med. 2016;8:437–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Ewers M, Biechele G, Suárez-Calvet M, Sacher C, Blume T, Morenas‐Rodriguez E, et al. Higher CSF sTREM2 and microglia activation are associated with slower rates of beta‐amyloid accumulation. EMBO Mol Med. 2020;12:e12308.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Zhong L, Xu Y, Zhuo R, Wang T, Wang K, Huang R, et al. Soluble TREM2 ameliorates pathological phenotypes by modulating microglial functions in an Alzheimer’s disease model. Nat Commun. 2019;10:1365.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Mawuenyega KG, Sigurdson W, Ovod V, Munsell L, Kasten T, Morris JC, et al. Decreased clearance of CNS β-Amyloid in Alzheimer’s Disease. Science. 2010;330:1774–1774.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Suárez-Calvet M, Kleinberger G, Araque Caballero MÁ, Brendel M, Rominger A, Alcolea D, et al. sTREM2 cerebrospinal fluid levels are a potential biomarker for microglia activity in early-stage Alzheimer’s disease and associate with neuronal injury markers. EMBO Mol Med. 2016;8:466–76.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Ma L-Z, Tan L, Bi Y-L, Shen X-N, Xu W, Ma Y-H, et al. Dynamic changes of CSF sTREM2 in preclinical Alzheimer’s disease: the CABLE study. Mol Neurodegeneration. 2020;15:25.

    Article  CAS  Google Scholar 

  17. Henjum K, Almdahl IS, Årskog V, Minthon L, Hansson O, Fladby T, et al. Cerebrospinal fluid soluble TREM2 in aging and Alzheimer’s disease. Alz Res Therapy. 2016;8:17.

    Article  Google Scholar 

  18. Piccio L, Deming Y, Del-Águila JL, Ghezzi L, Holtzman DM, Fagan AM, et al. Cerebrospinal fluid soluble TREM2 is higher in Alzheimer disease and associated with mutation status. Acta Neuropathol. 2016;131:925–33.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Guven G, Bilgic B, Samanci B, Gurvit H, Hanagasi H, Donmez C, et al. Peripheral TREM2 mRNA levels in early and late-onset Alzheimer disease’s patients. Mol Biol Rep. 2020;47:5903–9.

    Article  CAS  PubMed  Google Scholar 

  20. Casati M, Ferri E, Gussago C, Mazzola P, Abbate C, Bellelli G, et al. Increased expression of TREM2 in peripheral cells from mild cognitive impairment patients who progress into Alzheimer’s disease. Euro J Neurol. 2018;25:805–10.

    Article  CAS  Google Scholar 

  21. Heslegrave A, Heywood W, Paterson R, Magdalinou N, Svensson J, Johansson P, et al. Increased cerebrospinal fluid soluble TREM2 concentration in Alzheimer’s disease. Mol Neurodegener. 2016;11:3.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Leng F, Edison P. Neuroinflammation and microglial activation in Alzheimer disease: where do we go from here? Nat Rev Neurol. 2021;17:157–72.

    Article  PubMed  Google Scholar 

  23. Qu W, Li L. Microglial TREM2 at the intersection of Brain Aging and Alzheimer’s Disease. Neuroscientist. 2023;29:302–16.

    Article  CAS  PubMed  Google Scholar 

  24. Kwon HS, Koh S-H. Neuroinflammation in neurodegenerative disorders: the roles of microglia and astrocytes. Transl Neurodegener. 2020;9:42.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Wood H. Alzheimer disease: Soluble TREM2 in CSF sheds light on microglial activation in AD. Nat Rev Neurol. 2017;13:65.

    Article  CAS  PubMed  Google Scholar 

  26. Hu S, Pan N, Liu C, Wang Y, Zhang T. Age matching is essential for the study of Cerebrospinal Fluid sTREM2 levels and Alzheimer’s Disease Risk: a Meta-analysis. Front Aging Neurosci. 2021;13:775432.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Gao C, Jiang J, Tan Y, Chen S. Microglia in neurodegenerative diseases: mechanism and potential therapeutic targets. Sig Transduct Target Ther. 2023;8:359.

    Article  Google Scholar 

  28. Petersen RC, Aisen PS, Beckett LA, Donohue MC, Gamst AC, Harvey DJ, et al. Alzheimer’s Disease Neuroimaging Initiative (ADNI): clinical characterization. Neurology. 2010;74:201–9.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Ewers M, Franzmeier N, Suárez-Calvet M, Morenas-Rodriguez E, Caballero MAA, Kleinberger G, et al. Increased soluble TREM2 in cerebrospinal fluid is associated with reduced cognitive and clinical decline in Alzheimer’s disease. Sci Transl Med. 2019;11:eaav6221.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Suárez-Calvet M, Morenas-Rodríguez E, Kleinberger G, Schlepckow K, Araque Caballero MÁ, Franzmeier N, et al. Early increase of CSF sTREM2 in Alzheimer’s disease is associated with tau related-neurodegeneration but not with amyloid-β pathology. Mol Neurodegener. 2019;14:1.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Bittner T, Zetterberg H, Teunissen CE, Ostlund RE, Militello M, Andreasson U, et al. Technical performance of a novel, fully automated electrochemiluminescence immunoassay for the quantitation of β-amyloid (1–42) in human cerebrospinal fluid. Alzheimer’s Dement. 2016;12:517–26.

    Article  Google Scholar 

  32. Hansson O, Seibyl J, Stomrud E, Zetterberg H, Trojanowski JQ, Bittner T, et al. CSF biomarkers of Alzheimer’s disease concord with amyloid-β PET and predict clinical progression: a study of fully automated immunoassays in BioFINDER and ADNI cohorts. Alzheimer’s Dement. 2018;14:1470–81.

    Article  Google Scholar 

  33. Gisslén M, Heslegrave A, Veleva E, Yilmaz A, Andersson L-M, Hagberg L, et al. CSF concentrations of soluble TREM2 as a marker of microglial activation in HIV-1 infection. Neurol Neuroimmunol Neuroinflamm. 2019;6:e512.

    Article  PubMed  Google Scholar 

  34. Moore EE, Liu D, Li J, Schimmel SJ, Cambronero FE, Terry JG, et al. Association of Aortic Stiffness with Biomarkers of Neuroinflammation, synaptic dysfunction, and Neurodegeneration. Neurology. 2021;97:e329–40.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Cuciuc V, Tshori S, Grib L, Sella G, Tuvali O, Volodarsky I, et al. Circulating Soluble TREM2 and Cardiovascular Outcome in Cohort Study of Coronary Atherosclerosis patients. Int J Mol Sci. 2022;23:13121.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Wilson EN, Swarovski MS, Linortner P, Shahid M, Zuckerman AJ, Wang Q, et al. Soluble TREM2 is elevated in Parkinson’s disease subgroups with increased CSF tau. Brain. 2020;143:932–43.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Qin Q, Wan H, Wang D, Li J, Qu Y, Zhao J, et al. The Association of CSF sTREM2 with Cognitive decline and its dynamic change in Parkinson’s Disease: analysis of the PPMI Cohort. Front Aging Neurosci. 2022;14:892493.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  38. Del-Aguila JL, Benitez BA, Li Z, Dube U, Mihindukulasuriya KA, Budde JP, et al. TREM2 brain transcript-specific studies in AD and TREM2 mutation carriers. Mol Neurodegeneration. 2019;14:18.

    Article  Google Scholar 

  39. Frank S, Burbach GJ, Bonin M, Walter M, Streit W, Bechmann I, et al. TREM2 is upregulated in amyloid plaque-associated microglia in aged APP23 transgenic mice. Glia. 2008;56:1438–47.

    Article  PubMed  Google Scholar 

  40. Lue L-F, Schmitz CT, Serrano G, Sue LI, Beach TG, Walker DG. TREM2 protein expression changes correlate with Alzheimer’s Disease neurodegenerative pathologies in Post-mortem temporal cortices. Brain Pathol. 2015;25:469–80.

    Article  CAS  PubMed  Google Scholar 

  41. Forabosco P, Ramasamy A, Trabzuni D, Walker R, Smith C, Bras J, et al. Insights into TREM2 biology by network analysis of human brain gene expression data. Neurobiol Aging. 2013;34:2699–714.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  42. Suárez-Calvet M, Kleinberger G, Araque Caballero MÁ, Brendel M, Rominger A, Alcolea D, et al. sTREM 2 cerebrospinal fluid levels are a potential biomarker for microglia activity in early‐stage Alzheimer’s disease and associate with neuronal injury markers. EMBO Mol Med. 2016;8:466–76.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Morenas-Rodríguez E, Li Y, Nuscher B, Franzmeier N, Xiong C, Suárez-Calvet M, et al. Soluble TREM2 in CSF and its association with other biomarkers and cognition in autosomal-dominant Alzheimer’s disease: a longitudinal observational study. Lancet Neurol. 2022;21:329–41.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Schott JM, Revesz T. Inflammation in Alzheimer’s disease: insights from immunotherapy. Brain. 2013;136:2654–6.

    Article  PubMed  Google Scholar 

  45. Lehallier B, Gate D, Schaum N, Nanasi T, Lee SE, Yousef H, et al. Undulating changes in human plasma proteome profiles across the lifespan. Nat Med. 2019;25:1843–50.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Schindler SE, Cruchaga C, Joseph A, McCue L, Farias FHG, Wilkins CH, et al. African americans have differences in CSF Soluble TREM2 and Associated Genetic variants. Neurol Genet. 2021;7:e571.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Jay TR, Von Saucken VE, Landreth GE. TREM2 in neurodegenerative diseases. Mol Neurodegeneration. 2017;12:56.

    Article  Google Scholar 

  48. Lustig A, Liu HB, Metter EJ, An Y, Swaby MA, Elango P, et al. Telomere Shortening, Inflammatory cytokines, and anti-cytomegalovirus antibody follow distinct Age-Associated trajectories in humans. Front Immunol. 2017;8:1027.

    Article  PubMed  PubMed Central  Google Scholar 

  49. Sebastiani P, Thyagarajan B, Sun F, Schupf N, Newman AB, Montano M, et al. Biomarker signatures of aging. Aging Cell. 2017;16:329–38.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  50. Ferrucci L, Corsi A, Lauretani F, Bandinelli S, Bartali B, Taub DD, et al. The origins of age-related proinflammatory state. Blood. 2005;105:2294–9.

    Article  CAS  PubMed  Google Scholar 

  51. Sutphen CL, Jasielec MS, Shah AR, Macy EM, Xiong C, Vlassenko AG, et al. Longitudinal cerebrospinal fluid biomarker changes in preclinical Alzheimer Disease during Middle Age. JAMA Neurol. 2015;72:1029.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Suárez-Calvet M, Araque Caballero MÁ, Kleinberger G, Bateman RJ, Fagan AM, Morris JC et al. Early changes in CSF sTREM2 in dominantly inherited Alzheimer’s disease occur after amyloid deposition and neuronal injury. Sci Transl Med. 2016;8.

  53. Hua X, Hibar DP, Lee S, Toga AW, Jack CR, Weiner MW, et al. Sex and age differences in atrophic rates: an ADNI study with n = 1368 MRI scans. Neurobiol Aging. 2010;31:1463–80.

    Article  PubMed  PubMed Central  Google Scholar 

  54. Falcon C, Grau-Rivera O, Suárez-Calvet M, Bosch B, Sánchez-Valle R, Arenaza-Urquijo EM, et al. Sex differences of longitudinal brain changes in cognitively unimpaired adults. J Alzheimers Dis. 2020;76:1413–22.

    Article  PubMed  Google Scholar 

  55. Alvarez-De‐La‐Rosa M, Silva I, Nilsen J, Pérez MM, García‐Segura LM, Ávila J, et al. Estradiol prevents neural tau hyperphosphorylation characteristic of Alzheimer’s Disease. Ann N Y Acad Sci. 2005;1052:210–24.

    Article  PubMed  Google Scholar 

  56. Wang C, Zhang F, Jiang S, Siedlak SL, Shen L, Perry G, et al. Estrogen receptor-α is localized to neurofibrillary tangles in Alzheimer’s disease. Sci Rep. 2016;6:20352.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  57. Stephen TL, Cacciottolo M, Balu D, Morgan TE, LaDu MJ, Finch CE, et al. APOE genotype and sex affect microglial interactions with plaques in Alzheimer’s disease mice. acta Neuropathol Commun. 2019;7:82.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Moser VA, Workman MJ, Hurwitz SJ, Lipman RM, Pike CJ, Svendsen CN. Microglial transcription profiles in mouse and human are driven by APOE4 and sex. iScience. 2021;24:103238.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  59. Wood ME, Xiong LY, Wong YY, Buckley RF, Swardfager W, Masellis M, et al. Sex differences in associations between APOE ε2 and longitudinal cognitive decline. Alzheimer’s Dement. 2023;19:4651–61.

    Article  CAS  Google Scholar 

  60. Sampedro F, Vilaplana E, de Leon MJ, Alcolea D, Pegueroles J, Montal V, et al. APOE-by-sex interactions on brain structure and metabolism in healthy elderly controls. Oncotarget. 2015;6:26663–74.

    Article  PubMed  PubMed Central  Google Scholar 

  61. Hohman TJ, Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, et al. Sex-Specific Association of Apolipoprotein E with cerebrospinal fluid levels of tau. JAMA Neurol. 2018;75:989.

    Article  PubMed  PubMed Central  Google Scholar 

  62. Altmann A, Tian L, Henderson VW, Greicius MD. Alzheimer’s Disease Neuroimaging Initiative investigators. Sex modifies the APOE -related risk of developing Alzheimer disease. Ann Neurol. 2014;75:563–73.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Yan S, Zheng C, Paranjpe MD, Li J, Benzinger TLS, Lu J, et al. Association of sex and APOE ε4 with brain tau deposition and atrophy in older adults with Alzheimer’s disease. Theranostics. 2020;10:10563–72.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  64. Cacciaglia R, Salvadó G, Molinuevo JL, Shekari M, Falcon C, Operto G, et al. Age, sex and APOE-ε4 modify the balance between soluble and fibrillar β-amyloid in non-demented individuals: topographical patterns across two independent cohorts. Mol Psychiatry. 2022;27:2010–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Wang Y, Kang MS, Therriault J, Pascoal TA, Lussier FZ, Savard M, et al. APOE4 packs a punch in women: sex-specific vulnerability for tau and neuroinflammation: neuroimaging: sex and ethnoracial differences – biomarkers. Alzheimer’s Dement. 2020;16:e045098.

    Article  Google Scholar 

  66. Rozovsky I, Hoving S, Anderson CP, O’Callaghan J, Finch CE. Equine estrogens induce apolipoprotein E and glial fibrillary acidic protein in mixed glial cultures. Neurosci Lett. 2002;323:191–4.

    Article  CAS  PubMed  Google Scholar 

  67. Xu H, Gouras GK, Greenfield JP, Vincent B, Naslund J, Mazzarelli L, et al. Estrogen reduces neuronal generation of Alzheimer β-amyloid peptides. Nat Med. 1998;4:447–51.

    Article  CAS  PubMed  Google Scholar 

  68. Gamache J, Yun Y, Chiba-Falek O. Sex-dependent effect of APOE on Alzheimer’s disease and other age-related neurodegenerative disorders. Dis Models Mech. 2020;13:dmm045211.

    Article  CAS  Google Scholar 

  69. Dumurgier J, Paquet C, Benisty S, Kiffel C, Lidy C, Mouton-Liger F, et al. O4-06‐08: education level and CSF biomarkers in Alzheimer’s disease: the cognitive reserve theory. Alzheimer’s Dement. 2010;6:4SPart5.

    Article  Google Scholar 

  70. Dumurgier J, Paquet C, Benisty S, Kiffel C, Lidy C, Mouton-Liger F, et al. Inverse association between CSF Aβ 42 levels and years of education in mild form of Alzheimer’s disease: the cognitive reserve theory. Neurobiol Dis. 2010;40:456–9.

    Article  CAS  PubMed  Google Scholar 

  71. Bolton CJ, Zetterberg H, Blennow K, Jefferson AL, Hohman TJ, Gifford KA. Subjective cognitive decline interacts with sex and education on CSF β-Amyloid. Alzheimer’s Dement. 2022;18:e067881.

    Article  Google Scholar 

  72. Pa J, Aslanyan V, Casaletto KB, Rentería MA, Harrati A, Tom SE et al. Effects of Sex, APOE4, and Lifestyle Activities on Cognitive Reserve in older adults. Neurology. 2022;99.

  73. Alty JE, Bindoff AD, Stuart KE, Roccati E, Collins JM, King AE et al. Sex-specific Protective effects of Cognitive Reserve on Age-Related Cognitive decline: a 5-Year prospective cohort study. Neurology. 2023;100.

  74. Edison P, Archer HA, Gerhard A, Hinz R, Pavese N, Turkheimer FE, et al. Microglia, amyloid, and cognition in Alzheimer’s disease: an [11 C](R)PK11195-PET and [11 C]PIB-PET study. Neurobiol Dis. 2008;32:412–9.

    Article  CAS  PubMed  Google Scholar 

  75. Subhramanyam CS, Wang C, Hu Q, Dheen ST. Microglia-mediated neuroinflammation in neurodegenerative diseases. Semin Cell Dev Biol. 2019;94:112–20.

    Article  CAS  PubMed  Google Scholar 

  76. Dani M, Wood M, Mizoguchi R, Fan Z, Walker Z, Morgan R, et al. Microglial activation correlates in vivo with both tau and amyloid in Alzheimer’s disease. Brain. 2018;141:2740–54.

    PubMed  Google Scholar 

  77. Karlsson L, Vogel J, Arvidsson I, Åström K, Janelidze S, Blennow K, et al. Cerebrospinal fluid reference proteins increase accuracy and interpretability of biomarkers for brain diseases. Nat Commun. 2024;15:3676.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  78. Li Y, Yen D, Hendrix RD, Gordon BA, Dlamini S, Barthélemy NR, et al. Timing of Biomarker changes in sporadic Alzheimer’s disease in estimated years from Symptom Onset. Ann Neurol. 2024;95:951–65.

    Article  CAS  PubMed  Google Scholar 

  79. Vilalta A, Zhou Y, Sevalle J, Griffin JK, Satoh K, Allendorf DH, et al. Wild-type sTREM2 blocks Aβ aggregation and neurotoxicity, but the Alzheimer’s R47H mutant increases Aβ aggregation. J Biol Chem. 2021;296:100631.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  80. Power MC, Bennett EE, Turner RW, Dowling NM, Ciarleglio A, Glymour MM, et al. Trends in relative incidence and Prevalence of Dementia Across Non-hispanic Black and White Individuals in the United States, 2000–2016. JAMA Neurol. 2021;78:275.

    Article  PubMed  Google Scholar 

  81. Steenland K, Goldstein FC, Levey A, Wharton W. A Meta-Analysis of Alzheimer’s Disease Incidence and Prevalence Comparing African-Americans and Caucasians. 2017;:9.

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Acknowledgements

Data collection and sharing for this project was funded by the Alzheimer’s Disease Neuroimaging Initiative (ADNI) (National Institutes of Health Grant U01 AG024904) and DOD ADNI (Department of Defense award number W81XWH-12-2-0012). ADNI is funded by the National Institute on Aging, the National Institute of Biomedical Imaging and Bioengineering, and through generous contributions from the following: AbbVie, Alzheimer’s Association; Alzheimer’s Drug Discovery Foundation; Araclon Biotech; BioClinica, Inc.; Biogen; Bristol-Myers Squibb Company; CereSpir, Inc.; Cogstate; Eisai Inc.; Elan Pharmaceuticals, Inc.; Eli Lilly and Company; EuroImmun; F. Hofmann-La Roche Ltd. and its afliated company Genentech, Inc.; Fujirebio; GE Healthcare; IXICO Ltd.; Janssen Alzheimer Immunotherapy Research & Development, LLC.; Johnson & Johnson Pharmaceutical Research & Development LLC.; Lumosity; Lundbeck; Merck & Co., Inc.; Meso Scale Diagnostics, LLC.; NeuroRx Research; Neurotrack Technologies; Novartis Pharmaceuticals Corporation; Pfzer Inc.; Piramal Imaging; Servier; Takeda Pharmaceutical Company; and Transition Therapeutics. The Canadian Institutes of Health Research is providing funds to support ADNI clinical sites in Canada. Private sector contributions are facilitated by the Foundation for the National Institutes of Health (www.fnih.org). The grantee organization is the Northern California Institute for Research and Education, and the study is coordinated by the Alzheimer’s Therapeutic Research Institute at the University of Southern California. ADNI data are disseminated by the Laboratory for Neuro Imaging at the University of Southern California. Data used in the preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at: http://adni.loni.usc.edu/wp-content/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf.

Funding

The study was supported by Sun Yat-Sen University and the Pearl River Scholar Program of Guangdong Province (Health Science Section, No: 0920220206).

Open access funding provided by Karolinska Institute.

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Authors and Affiliations

  1. Department of Epidemiology, School of Public Health (Shenzhen), Sun Yat-Sen University, Shenzhen, China

    Yu Wang, Meijie Ye, Qianqian Ji, Qi Liu & Yiqiang Zhan

  2. Department of Neurology, The Seventh Affiliated Hospital of Sun Yat-Sen University, Shenzhen, China

    Xiaowei Xu

  3. Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden

    Yiqiang Zhan

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  1. Yu Wang
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Contributions

YZ conceptualized the study, analyzed, and interpreted the data, and drafted and revised the manuscript. YW, MY, QJ, and QL analyzed and interpreted the data, drafted and revised the manuscript, did the statistical analysis, and prepared all the figures. XX contributed to the interpretation of the data and revision of the manuscript.

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Correspondence to Xiaowei Xu or Yiqiang Zhan.

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Ethics approval and consent to participate

The study was approved by institutional review boards of all participating institutions, and written informed consent was obtained from all participants or their guardians according to the Declaration of Helsinki (consent for research). All work complied with ethical regulations for working with human participants. Ethics approval was obtained from the institutional review boards of each institution involved: Oregon Health and Science University; University of Southern California; University of California—San Diego; University of Michigan; Mayo Clinic, Rochester; Baylor College of Medicine; Columbia University Medical Center; Washington University, St. Louis; University of Alabama at Birmingham; Mount Sinai School of Medicine; Rush University Medical Center; Wien Center; Johns Hopkins University; New York University; Duke University Medical Center; University of Pennsylvania; University of Kentucky; University of Pittsburgh; University of Rochester Medical Center; University of California, Irvine; University of Texas Southwestern Medical School; Emory University; University of Kansas, Medical Center; University of California, Los Angeles; Mayo Clinic, Jacksonville; Indiana University; Yale University School of Medicine; McGill University, Montreal-Jewish General Hospital; Sunnybrook Health Sciences, Ontario; U.B.C. Clinic for AD & Related Disorders; Cognitive Neurology—St. Joseph’s, Ontario; Cleveland Clinic Lou Ruvo Center for Brain Health; Northwestern University; Premiere Research Inst (Palm Beach Neurology); Georgetown University Medical Center; Brigham and Women’s Hospital; Stanford University; Banner Sun Health Research Institute; Boston University; Howard University; Case Western Reserve University; University of California, Davis—Sacramento; Neurological Care of CNY; Parkwood Hospital; University of Wisconsin; University of California, Irvine—BIC; Banner Alzheimer’s Institute; Dent Neurologic Institute; Ohio State University; Albany Medical College; Hartford Hospital, Olin Neuropsychiatry Research Center; Dartmouth-Hitchcock Medical Center; Wake Forest University Health Sciences; Rhode Island Hospital; Butler Hospital; UC San Francisco; Medical University South Carolina; St. Joseph’s Health Care Nathan Kline Institute; University of Iowa College of Medicine; Cornell University and University of South Florida: USF Health Byrd Alzheimer’s Institute.

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Wang, Y., Ye, M., Ji, Q. et al. The longitudinal trajectory of CSF sTREM2: the alzheimer’s disease neuroimaging initiative. Alz Res Therapy 16, 138 (2024). https://doiorg.publicaciones.saludcastillayleon.es/10.1186/s13195-024-01506-8

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Keywords

Alzheimer's Research & Therapy

ISSN: 1758-9193