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  • 1
    In: Human Brain Mapping, Wiley, Vol. 44, No. 2 ( 2023-02), p. 535-548
    Abstract: Sex differences in white matter microstructure have been robustly demonstrated in the adult brain using both conventional and advanced diffusion‐weighted magnetic resonance imaging approaches. However, sex differences in white matter microstructure prior to adulthood remain poorly understood; previous developmental work focused on conventional microstructure metrics and yielded mixed results. Here, we rigorously characterized sex differences in white matter microstructure among over 6000 children from the Adolescent Brain Cognitive Development study who were between 9 and 10 years old. Microstructure was quantified using both the conventional model—diffusion tensor imaging (DTI)—and an advanced model, restriction spectrum imaging (RSI). DTI metrics included fractional anisotropy (FA) and mean, axial, and radial diffusivity (MD, AD, RD). RSI metrics included normalized isotropic, directional, and total intracellular diffusion (N0, ND, NT). We found significant and replicable sex differences in DTI or RSI microstructure metrics in every white matter region examined across the brain. Sex differences in FA were regionally specific. Across white matter regions, boys exhibited greater MD, AD, and RD than girls, on average. Girls displayed increased N0, ND, and NT compared to boys, on average, suggesting greater cell and neurite density in girls. Together, these robust and replicable findings provide an important foundation for understanding sex differences in health and disease.
    Type of Medium: Online Resource
    ISSN: 1065-9471 , 1097-0193
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 1492703-2
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  • 2
    In: JAMA Psychiatry, American Medical Association (AMA), Vol. 71, No. 4 ( 2014-04-01), p. 375-
    Type of Medium: Online Resource
    ISSN: 2168-622X
    Language: English
    Publisher: American Medical Association (AMA)
    Publication Date: 2014
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  • 3
    In: Alzheimer's & Dementia, Wiley, Vol. 17, No. S4 ( 2021-12)
    Abstract: The incidence of dementia in India is 14%, and its prevalence doubles with every five‐year increase in age. Given the lack of ethnic diversity in most brain research to date, it is valuable to study cohorts with diverse genetic and environmental backgrounds, to identify predictors of health and disease that can be generalized to other ethnic groups than the commonly studied populations of European ancestry. To address this gap in the literature, we modeled factors that affect aging patterns in the brain’s white matter in individuals with Indian ancestry using advanced diffusion‐weighted MRI (dMRI). Method Cross‐sectional dMRI data from 123 individuals (males, n=78; females, n=45) of self‐reported Indian ancestry (born in India: 44%; mean age: 60.1±8.3 SD, range: 45‐80) from the UK Biobank were analyzed using diffusion tensor imaging (DTI), the tensor distribution function (TDF), neurite orientation dispersion and density imaging (NODDI) and mean apparent propagator MRI (MAPMRI). Main effects of age, sex, and age‐by‐sex interaction were investigated to characterize trajectories in whole‐brain white matter averages and the corpus callosum (CC), parcellated using the JHU‐ICBM atlas, covarying for years of education, waist/hip ratio, population structure (Figure 1) and the Townsend index. Normative lifespan charts were created to visualize white matter aging trajectories for the major diffusivity metrics. Result Normative centile curves (Figures 2‐3) show, with increasing age, declining white matter integrity, increased diffusivity, lower white matter density and diffusion restriction at the whole‐brain level and CC (Table 1; Figure 4). There was no detectable effect of sex, nor age‐by‐sex interaction, across whole‐brain metrics. In the CC, a steeper aging trajectory, evidenced by more pronounced white matter changes, was observed in males relative to females (Table 1; Figure 5). Conclusion Using advanced dMRI modeling, we report diffuse white matter changes with respect to age in a subsample of UK Biobank individuals of self‐reported Indian ancestry. Future studies should include larger sample sizes, comparisons with Indian ancestry individuals residing in India, consider vascular factors, and examine genotype interactions (e.g., with apolipoprotein E genotype), to further characterize risk factors and better understand brain aging in diverse populations with varied genetic and environmental backgrounds.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2201940-6
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  • 4
    In: Alzheimer's & Dementia, Wiley, Vol. 16, No. S4 ( 2020-12)
    Abstract: Much remains to be understood about subcortical brain alterations across the lifespan and how such changes are related to sex and genetic risk for dementia. Here we analyze the effect of sex, age and APOE genotype on subcortical volume and high‐resolution morphometry in a large population‐based sample. We hypothesized that shape analysis would reveal complex age and sex effects not revealed by gross volumetric analysis and that each copy of the APOE 4 alele would be associated with smaller hippocampal volume. Method T1‐weighted brain MRI data (N=9,872) from the UK Biobank were processed using FreeSurfer v5.3 to derive bilateral hippocampus, thalamus, putamen, pallidum, amygdala, caudate, nucleus accumbens, lateral ventricle and intracranial volumes (ICV). The ENIGMA Shape Analysis Pipeline was used to compute local thickness and surface area (SA) metrics for up to 2,502 vertices along each structure’s surface (Figure 1). Linear regression was used to model age (44‐79 yrs), sex, age‐by‐sex interactions, and APOE genotype (Table 1) associations with gross volumes and shape metrics while adjusting for age 2 , ICV, years of education and body mass index, and adjusting for multiple comparisons. Result Older individuals had generally lower gross volumes and larger lateral ventricles (Table 2). Males tended to have larger volumes compared to females (Table 2), though shape analysis revealed subregions that were larger in females (Figure 2). In the full cohort, a significant age‐by‐sex interaction showed males had lower volumes with increasing age. However, in individuals over 60, this interaction was significantly attenuated (Table 2). Shape analysis revealed age‐by‐sex interactions to be more complex, with females displaying subregions of lower thickness and SA with increasing age. No effect of APOE genotype nor interaction between age, sex and genotype were observed, possibly due to small samples of APOE e2/2 and e4/4 genotypes. Conclusion Here we show that age and sex effects on subcortical structures may be more complex when modeled using local shape morphometric features. While males tended to lose volume faster than females over the full age span, these effects were weaker at more advanced ages ( 〉 60), indicating potentially complex and differential brain aging patterns in men and women.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2201940-6
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  • 5
    In: Alzheimer's & Dementia, Wiley, Vol. 17, No. S4 ( 2021-12)
    Abstract: Understanding the normative variation in brain structure across life may provide insights into healthy aging as well as neurological disorders such as Alzheimer’s disease (AD). Women are at greater risk of developing AD, but men tend to show faster rates of subcortical atrophy across adulthood. Sex‐dependent differences in male and female brain aging trajectories may change over the adult lifespan, and could play a role in differential risk for neurological illness. The current study maps normative trajectories (nomograms) of subcortical volume across adulthood and quantifies the interaction between age and sex in a large, healthy sample. Method T1‐weighted brain MRI from a sample of UK Biobank participants free from psychiatric/neurological illness (; N=39,544; 44.6‐82.8 years) were segmented using FreeSurfer 7.1 to derive average left and right thalamus, putamen, pallidum, hippocampus, amygdala, caudate, nucleus accumbens and ventricle volumes. Normative quantile regression models (nomograms) were created to visualize aging trajectories for each volume. Linear mixed models were fit in binned age groups to assess age‐by‐sex interactions across middle to late adulthood. Result Nomograms showed volumetric loss across adulthood, except for ventricular volume which was larger with increasing age (). Compared to females, males showed a steeper slope of volume change with increasing age in all regions across the full age range (Cohen’s d : ‐0.14 ‐ 0.12) (). Binned‐age analysis showed males to have steeper volume loss trajectories in middle adulthood, with fewer age‐by‐sex interactions detected later in life for most structures. Conclusion In a large sample of healthy adults, we found a structure‐specific interaction between age and sex, with males tending to show steeper age‐related volume loss trajectories compared to females until later decades of life, where trends appeared similar for men and women. This study provides normative subcortical aging trends and identifies potential sex‐dependent variations across life that may be used to understand healthy brain aging and risk for disorders such as AD.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2201940-6
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  • 6
    In: Alzheimer's & Dementia, Wiley, Vol. 18, No. S5 ( 2022-12)
    Abstract: Aging and Alzheimer’s disease (AD) are associated with alterations in the brain’s white matter (WM) microstructure. AD also exhibits significant sex differences and, similar to age, sex has also been associated with WM microstructural variability. A comprehensive characterization of how aging and sex impact WM microstructure may thus improve our understanding of processes involved in AD. Here we examined age and sex effects on traditional and advanced measures of WM microstructure in middle‐ to older‐aged adults. Method Cross‐sectional diffusion‐weighted MRI (dMRI) scans were analyzed from 34,423 UK Biobank participants (aged 45‐80 years; 53% female) using single‐shell models (DTI, TDF), and advanced multi‐shell models (NODDI, MAP). Metrics were projected to a standard WM skeleton using publicly available ENIGMA protocols, based on TBSS (FSL). Mean values for each dMRI metric were extracted from the whole WM skeleton, and age was modeled using fractional polynomial regressions, co‐varying for years of education, waist/hip ratio, population structure, and the Townsend index. Sex‐stratified centile curves were created for each dMRI metric to provide normative reference charts. Result WM microstructure across the brain was significantly associated with participants’ age and sex for all dMRI models (main effects, ps 〈 .001). Increasing age in our cross‐sectional sample was associated with lower anisotropy (DTI‐FA, TDF‐FA), neurite density (NODDI‐ICVF, MAP‐RTOP, MAPMRI‐RTAP), and restriction (MAP‐RTPP) as well as higher diffusivity (DTI‐AxD, DTI‐MD, DTI‐RD), free water (NODDI‐ISOVF), and white matter dispersion (NODDI‐OD) for both males and females ( Figures 1 and 2 ). Some metrics showed a gentle decline until around age 60, followed by a precipitous decline thereafter (e.g., TDF‐FA, NODDI‐ICVF, MAP‐RTAP, Figures 1 and 2 ). Significant sex differences in aging were most sensitively detected by the advanced dMRI multi‐shell models NODDI and MAPMRI (age‐by‐sex interaction; males showing a steeper trajectory for NODDI‐OD, p 〈 .001, females showing a steeper trajectory for MAPMRI‐RTPP, p 〈 .01, with age). Conclusion Participant age and sex are significantly associated with the brain’s WM microstructure; advanced dMRI models displayed the greatest sensitivity, strenghtening previous findings in a smaller UKB sample (15k). Along with our calculated centile curves, we offer an important normative reference to guide future studies of Alzheimer’s disease.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2022
    detail.hit.zdb_id: 2201940-6
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  • 7
    In: Brain Imaging and Behavior, Springer Science and Business Media LLC, Vol. 15, No. 6 ( 2021-12), p. 2813-2823
    Abstract: A comprehensive characterization of the brain’s white matter is critical for improving our understanding of healthy and diseased aging. Here we used diffusion-weighted magnetic resonance imaging (dMRI) to estimate age and sex effects on white matter microstructure in a cross-sectional sample of 15,628 adults aged 45–80 years old (47.6% male, 52.4% female). Microstructure was assessed using the following four models: a conventional single-shell model, diffusion tensor imaging (DTI); a more advanced single-shell model, the tensor distribution function (TDF); an advanced multi-shell model, neurite orientation dispersion and density imaging (NODDI); and another advanced multi-shell model, mean apparent propagator MRI (MAPMRI). Age was modeled using a data-driven statistical approach, and normative centile curves were created to provide sex-stratified white matter reference charts. Participant age and sex substantially impacted many aspects of white matter microstructure across the brain, with the advanced dMRI models TDF and NODDI detecting such effects the most sensitively. These findings and the normative reference curves provide an important foundation for the study of healthy and diseased brain aging.
    Type of Medium: Online Resource
    ISSN: 1931-7557 , 1931-7565
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2021
    detail.hit.zdb_id: 2377165-3
    SSG: 5,2
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  • 8
    In: Psychiatry Research: Neuroimaging, Elsevier BV, Vol. 291 ( 2019-09), p. 1-8
    Type of Medium: Online Resource
    ISSN: 0925-4927
    RVK:
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2019
    detail.hit.zdb_id: 1500675-X
    detail.hit.zdb_id: 2900605-3
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  • 9
    In: Brain, Oxford University Press (OUP), Vol. 138, No. 7 ( 2015-07), p. 2087-2102
    Type of Medium: Online Resource
    ISSN: 0006-8950 , 1460-2156
    RVK:
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2015
    detail.hit.zdb_id: 1474117-9
    SSG: 12
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  • 10
    In: Alzheimer's & Dementia, Wiley, Vol. 16, No. S4 ( 2020-12)
    Abstract: Common variants in the APOE gene are associated with cognitive decline, brain atrophy and risk for developing Alzheimer’s disease (AD). APOE polymorphism effects may also vary with age, sex, body mass index (BMI), and other risk factors. Here we create percentile charts ‐ or ‘nomograms’ ‐ plotting the trajectory of subcortical volumes with age, stratified by sex and by APOE genotype, in a large population‐based sample from the UK Biobank. We hypothesized that age effects would differ in men and women and APOE e4 allele carriers would tend to show steeper age‐related decline compared to those carrying APOE e3 and e2 genotypes. Method T1‐weighted brain MRI UK Biobank data (N=9,414; age range: 44‐79 yrs (Table 1) were processed using FreeSurfer v5.3 to derive quality inspected volumes averaged across hemispheres: lateral ventricles, hippocampus, thalamus, putamen, pallidum, amygdala, caudate, nucleus accumbens, and intracranial volume (ICV). The R package rstandard was used to adjust subcortical volumes for effects of ICV and BMI. R package GAMLSS , specifically the centile function, was used to compute percentile curves for each ROI based on standardized residuals, with ROI volume as the dependent variable and age as the independent variable. Separate models were fitted by sex and for each APOE genotype and visualized for trends with age. Result Nomograms for the full cohort showed trends for increasing lateral ventricle and decreasing thalamus, putamen, hippocampus, amygdala, and nucleus accumbens volumes with increasing age (Figures 1‐2). In men, volumes decreased at a faster rate until age 60, when volumetric decline in women appeared to accelerate and catch up with males. Nomograms separated by APOE genotype (Figure 1) all followed similar patterns, though smaller samples of APOE e2/2 and e4/4 genotypes limit the interpretability of those age trends. Conclusion Nomograms plotted by sex show a differential age trajectory for men and women offering clues for future sex‐dependent brain related assessment and intervention. APOE genotype did not strongly influence nomograms, though a greater number of APOE e2/2 and e4/4 individuals are needed to obtain reliable normative trends.
    Type of Medium: Online Resource
    ISSN: 1552-5260 , 1552-5279
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2201940-6
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