医学
混淆
炎症
生物标志物
免疫学
性别特征
性激素结合球蛋白
血液蛋白质类
人类免疫缺陷病毒(HIV)
内科学
生理学
激素
年轻人
队列
结合珠蛋白
蛋白质组
免疫衰老
C反应蛋白
全身炎症
急性期蛋白
转录组
流行病学
队列研究
炎症反应
干扰素
内分泌学
作者
Rebecca Abelman,Samuel R Schnittman,Natália Faraj Murad,Adam B. Olshen,Gabriele Beck‐Engeser,Nayara S. S. Aquino,Gabrielle C. Ambayec,Edward R. Cachay,Joseph J. Eron,Michael S Saag,Robin M. Nance,Joseph A. Delaney,Stephanie A. Ruderman,Richard D. Moore,Kenneth H. Mayer,Jeffrey M. Jacobson,Heidi M. Crane,Peter W. Hunt
摘要
BACKGROUNDAmong antiretroviral therapy-suppressed (ART-suppressed) people with HIV (PWH), women have higher levels of some inflammatory markers than men, but the effect of sex on the inflammatory proteome, and whether age modifies these differences, remain unclear.METHODSPlasma inflammatory protein levels were assessed in ART-suppressed PWH from the Center for AIDS Research Network of Integrated Clinical Systems. The relationship between sex and plasma proteins - including 22 interferon-α response pathway proteins - was assessed, adjusting for confounders and assessing interactions by age.RESULTSOf 922 participants, 162 (18%) were female. The median age was 47, above which the majority of women had undetectable plasma anti-Müllerian hormone levels, a biomarker of ovarian reserve. Age modified the influence of sex on the inflammatory proteome. Older age (>47) was associated with greater increases among women than men in 194 proteins. Interferon-α response proteins were higher in men in those ≤ 47 but higher in women in those > 47 (interaction P < 0.001). Among the 131 proteins associated with mortality risk (q < 0.05), only 5 differed by sex among those ≤ 47, while 79 differed by sex in those > 47, with nearly all being higher in women. Women had decreased mortality than men ≤ 47 (P < 0.001) but had similar mortality > 47 (P = 0.84).CONCLUSIONThe menopausal transition appears to increase systemic type I interferon responses and inflammation in women with HIV, which may contribute to a loss of female advantage in mortality.FUNDINGNIH National Heart, Lung, and Blood Institute; National Institute of Neurological Disorders and Stroke; National Institute of Allergy and Infectious Diseases.
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