Genetic ancestry and population differences in levels of inflammatory cytokines in women: Role for evolutionary selection and environmental factors.
Web of Science
AuthorYao, S; Hong, C-C; Ruiz-Narváez, EA; Evans, SS; Zhu, Q; Schaefer, BA; Yan, L; Coignet, MV; Lunetta, KL; Sucheston-Campbell, LE; ...
Source TitlePLoS Genetics
PublisherPublic Library of Science (PLoS)
University of Melbourne Author/sBaglietto, Laura
AffiliationMelbourne School of Population and Global Health
Document TypeJournal Article
CitationsYao, S., Hong, C. -C., Ruiz-Narváez, E. A., Evans, S. S., Zhu, Q., Schaefer, B. A., Yan, L., Coignet, M. V., Lunetta, K. L., Sucheston-Campbell, L. E., Lee, K., Bandera, E. V., Troester, M. A., Rosenberg, L., Palmer, J. R., Olshan, A. F. & Ambrosone, C. B. (2018). Genetic ancestry and population differences in levels of inflammatory cytokines in women: Role for evolutionary selection and environmental factors.. PLoS Genet, 14 (6), pp.e1007368-. https://doi.org/10.1371/journal.pgen.1007368.
Access StatusOpen Access
Open Access at PMChttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991662
Selection pressure due to exposure to infectious pathogens endemic to Africa may explain distinct genetic variations in immune response genes. However, the impact of those genetic variations on human immunity remains understudied, especially within the context of modern lifestyles and living environments, which are drastically different from early humans in sub Saharan Africa. There are few data on population differences in constitutional immune environment, where genetic ancestry and environment are likely two primary sources of variation. In a study integrating genetic, molecular and epidemiologic data, we examined population differences in plasma levels of 14 cytokines involved in innate and adaptive immunity, including those implicated in chronic inflammation, and possible contributing factors to such differences, in 914 AA and 855 EA women. We observed significant differences in 7 cytokines, including higher plasma levels of CCL2, CCL11, IL4 and IL10 in EAs and higher levels of IL1RA and IFNα2 in AAs. Analyses of a wide range of demographic and lifestyle factors showed significant impact, with age, education level, obesity, smoking, and alcohol intake, accounting for some, but not all, observed population differences for the cytokines examined. Levels of two pro-inflammatory chemokines, CCL2 and CCL11, were strongly associated with percent of African ancestry among AAs. Through admixture mapping, the signal was pinpointed to local ancestry at 1q23, with fine-mapping analysis refined to the Duffy-null allele of rs2814778. In AA women, this variant was a major determinant of systemic levels of CCL2 (p = 1.1e-58) and CCL11 (p = 2.2e-110), accounting for 19% and 40% of the phenotypic variance, respectively. Our data reveal strong ancestral footprints in inflammatory chemokine regulation. The Duffy-null allele may indicate a loss of the buffering function for chemokine levels. The substantial immune differences by ancestry may have broad implications to health disparities between AA and EA populations.
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