Exploring the Effects of Ethnicity, Sex, and APOE Status on Markers of Inflammation

Abstract Background Alzheimer’s Disease (AD) is the most common form of dementia and is considered to disproportionately affect underserved populations like Hispanics/Latinos. Most research available with AD markers such as inflammation and APOE4 has been conducted in predominantly White cohorts, leaving a dearth of knowledge relating APOE4 and inflammation in Hispanic/Latinos. Recent research also suggests inflammation and AD risk may be sex‐specific. This study investigated the effects of race/ethnicity, sex/gender, and APOE4 on inflammatory markers. Method Using data from the Health and Aging Brain Study‐Health Disparities (HABS‐HD), we assessed group differences between APOE4 status, ethnicity, and sex on anti‐inflammatory marker interleukin‐10 covarying for age and education. Result The dataset included 817 Mexican Americans (65% women, 18% APOE4 carrier, mean age±SD=63.21±8.04 years) and 746 white participants (54% women, 30% APOE4 carrier, mean age±SD=68.59±8.70 years) (Table 1). We found two‐way interactions between sex and race/ethnicity (p=0.03) on IL‐10, driven by higher IL‐10 levels in Mexican American men; sex and APOE4 status (p=0.001), driven by higher IL‐10 among APOE4 carriers in men; and race/ethnicity and APOE4 status (p=0.001), driven by higher IL‐10 levels APOE4 carriers among Mexican Americans (Figure 1A,B and C respectively). Conclusion IL‐10 is an important anti‐inflammatory modulator of glial activation, preventing inflammation‐mediated neuronal degeneration under pathological conditions. It has multiple immunoregulatory effects such as in ability to inhibit the production of several inflammatory cytokines. These findings support previous studies demonstrating heightened systemic inflammation in APOE4 carriers, but little has been shown regarding their relationship with gender and ethnicity. This finding suggests the importance of examining differences that may exist between APOE4, sex, and inflammatory markers in Hispanics/Latinos. Future work will examine other inflammatory markers.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.091862
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
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article

Exploring the Effects of Ethnicity, Sex, and APOE Status on Markers of Inflammation

Judy Pa, Vahan Aslanyan, Joey A. Contreras, Nancy E Ortega
Alzheimer s & Dementia
Neuroinflammation and Neurodegeneration Mechanisms
article

Exploring the Effects of Ethnicity, Sex, and APOE Status on Markers of Inflammation

Judy Pa, Vahan Aslanyan, Joey A. Contreras, Nancy E Ortega
article en

Abstract

Abstract Background Alzheimer’s Disease (AD) is the most common form of dementia and is considered to disproportionately affect underserved populations like Hispanics/Latinos. Most research available with AD markers such as inflammation and APOE4 has been conducted in predominantly White cohorts, leaving a dearth of knowledge relating APOE4 and inflammation in Hispanic/Latinos. Recent research also suggests inflammation and AD risk may be sex‐specific. This study investigated the effects of race/ethnicity, sex/gender, and APOE4 on inflammatory markers. Method Using data from the Health and Aging Brain Study‐Health Disparities (HABS‐HD), we assessed group differences between APOE4 status, ethnicity, and sex on anti‐inflammatory marker interleukin‐10 covarying for age and education. Result The dataset included 817 Mexican Americans (65% women, 18% APOE4 carrier, mean age±SD=63.21±8.04 years) and 746 white participants (54% women, 30% APOE4 carrier, mean age±SD=68.59±8.70 years) (Table 1). We found two‐way interactions between sex and race/ethnicity (p=0.03) on IL‐10, driven by higher IL‐10 levels in Mexican American men; sex and APOE4 status (p=0.001), driven by higher IL‐10 among APOE4 carriers in men; and race/ethnicity and APOE4 status (p=0.001), driven by higher IL‐10 levels APOE4 carriers among Mexican Americans (Figure 1A,B and C respectively). Conclusion IL‐10 is an important anti‐inflammatory modulator of glial activation, preventing inflammation‐mediated neuronal degeneration under pathological conditions. It has multiple immunoregulatory effects such as in ability to inhibit the production of several inflammatory cytokines. These findings support previous studies demonstrating heightened systemic inflammation in APOE4 carriers, but little has been shown regarding their relationship with gender and ethnicity. This finding suggests the importance of examining differences that may exist between APOE4, sex, and inflammatory markers in Hispanics/Latinos. Future work will examine other inflammatory markers.

Alzheimer s & DementiaVol. 20(S2)
University of Southern California (US), University of California San Diego (US), Alzheimer’s Disease Neuroimaging Initiative (US)
Openalex Percentile: Top 71%
Neuroinflammation and Neurodegeneration Mechanisms
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