Wada Nikolas I, Breen Elizabeth C, Post Wendy S, Stosor Valentina, Macatangay Bernard J, Margolick Joseph B
Novel Coronavirus Research Compendium, Johns Hopkins University, Baltimore, Maryland, USA.
Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, University of California-Los Angeles, USA.
J Gerontol A Biol Sci Med Sci. 2022 Jul 5;77(7):1382-1388. doi: 10.1093/gerona/glab190.
C-reactive protein (CRP) is an inflammatory biomarker associated with all-cause mortality and morbidities such as cardiovascular disease. CRP is increased with HIV infection and thought to increase with age, though trajectories of CRP with aging have not been well characterized. We investigated trajectories of CRP in men from the Multicenter AIDS Cohort Study, according to HIV infection and HIV viral load status.
CRP measurements from 12 250 serum samples, provided by 2132 men over a span of 30 years, were categorized by HIV status at sample collection: HIV uninfected (HIV-, n = 1717), HIV infected with undetectable RNA (HIV+ suppressed, n = 4075), and detectable HIV RNA (HIV+ detectable, n = 6458). Age-related trajectories of CRP were fit to multivariable linear mixed models; we tested for differences in trajectories by HIV status.
CRP increased with age in all sample groups. HIV+ detectable and HIV+ suppressed samples had higher CRP than HIV- samples throughout the observed age range of 20-70 years (p < .05). CRP concentrations at age 45 years were 38% (95% CI: 26%-50%) and 26% (15%-38%) higher in HIV+ detectable and HIV+ suppressed samples, respectively, relative to HIV- samples. HIV+ detectable samples showed more rapid linear increases with age (8% higher/decade, 0.3%-16%) than HIV- samples.
We observed higher concentrations of CRP across 5 decades of age in men living with HIV, and steeper increases with age in men with detectable HIV RNA, relative to HIV- men. These results are consistent with a contribution of inflammation to the higher risk of age-related comorbidities with HIV infection.
C反应蛋白(CRP)是一种炎症生物标志物,与全因死亡率和心血管疾病等发病率相关。CRP在HIV感染时会升高,并且一般认为会随着年龄增长而升高,不过CRP随年龄增长的变化轨迹尚未得到充分描述。我们根据HIV感染情况和HIV病毒载量状态,研究了多中心艾滋病队列研究中男性的CRP变化轨迹。
在30年期间,由2132名男性提供的12250份血清样本的CRP测量值,根据样本采集时的HIV状态进行分类:未感染HIV(HIV-,n = 1717)、HIV感染但RNA检测不到(HIV+ 病毒抑制,n = 4075)以及HIV RNA可检测到(HIV+ 可检测,n = 6458)。将CRP的年龄相关变化轨迹拟合到多变量线性混合模型中;我们检验了不同HIV状态下变化轨迹的差异。
在所有样本组中,CRP均随年龄增长而升高。在20至70岁的整个观察年龄范围内,HIV+ 可检测和HIV+ 病毒抑制样本的CRP均高于HIV- 样本(p < 0.05)。相对于HIV- 样本,45岁时HIV+ 可检测和HIV+ 病毒抑制样本中的CRP浓度分别高出38%(95% CI:26% - 50%)和26%(15% - 38%)。与HIV- 样本相比,HIV+ 可检测样本随年龄增长呈现出更快的线性升高(每十年高出8%,0.3% - 16%)。
我们观察到,在5个十年的年龄跨度中,HIV感染者的CRP浓度更高,相对于未感染HIV的男性,HIV RNA可检测到的男性随年龄增长CRP升高更为显著。这些结果与炎症导致HIV感染相关的年龄相关性合并症风险增加相符。