Department of Anthropology, Northwestern University, Evanston, Illinois, USA.
Am J Hum Biol. 2012 Sep-Oct;24(5):675-81. doi: 10.1002/ajhb.22296. Epub 2012 May 26.
C-reactive protein (CRP) is a central component of innate immune defenses, and high sensitivity CRP has emerged as an important biomarker of chronic inflammation and cardiovascular disease risk. Prior analyses of CRP variability have reported stable between-individual differences in CRP over time, but a limitation of current knowledge is that it is based on research conducted in post-epidemiologic transition populations.
This study evaluated CRP variability among adults in the southeastern region of the Ecuadorian Amazon where rates of infectious diseases remain high. Blood samples were collected from 52 adults at four weekly sampling intervals and were quantified using a high-sensitivity immunoassay.
Median CRP concentration was 0.52 mg/l. About 34.6% of participants had CRP >3 mg/l at one time point, but no individuals had CRP >3 mg/l across two or more sampling intervals, and within-individual correlations revealed low levels of stable, between-individual differences in CRP. The application of current guidelines for the assessment of chronic inflammation failed to detect a single case of "high risk" CRP.
This study is the first to investigate CRP variability in a nonindustrialized, high infectious disease environment. It documents a pattern of variation over time that is distinct from prior research, with no evidence for chronic low-grade inflammation. These results may have substantial implications for research on inflammation and diseases of aging globally, as well as for scientific understandings of the regulation of inflammation.
C 反应蛋白(CRP)是先天免疫防御的核心组成部分,高敏 CRP 已成为慢性炎症和心血管疾病风险的重要生物标志物。先前对 CRP 变异性的分析报告称,CRP 个体间差异在一段时间内相对稳定,但现有知识的局限性在于,它是基于后流行病学转变人群的研究得出的。
本研究评估了厄瓜多尔亚马逊东南部地区成年人的 CRP 变异性,该地区传染病发病率仍然很高。从 52 名成年人中采集了 4 周的血液样本,并使用高敏免疫分析法进行定量。
CRP 浓度中位数为 0.52 毫克/升。约 34.6%的参与者在一个时间点 CRP >3 毫克/升,但没有一个人在两个或更多采样间隔 CRP >3 毫克/升,个体内相关性显示 CRP 个体间差异稳定,水平较低。当前用于评估慢性炎症的指南的应用未能检测到一例“高风险”CRP。
本研究首次在非工业化、高传染病环境中研究 CRP 变异性。它记录了一种与以往研究不同的时间变化模式,没有慢性低度炎症的证据。这些结果可能对全球炎症和衰老相关疾病的研究以及对炎症调节的科学认识具有重要意义。