International Centre for Eye Health, London School of Hygiene & Tropical Medicine, London, United Kingdom.
J Acquir Immune Defic Syndr. 2013 Jan 1;62(1):43-51. doi: 10.1097/QAI.0b013e318273b631.
Some evidence suggests that HIV infection is associated with premature frailty-a syndrome typically viewed as being related to ageing. We determined the prevalence and predictors of frailty in a population of HIV-infected individuals in South Africa.
Case-control study of 504 adults more than the age of 30 years, composed of 248 HIV-infected adults and 256 age- and gender-matched, frequency-matched HIV-seronegative individuals.
Frailty was defined by standardized assessment comprised of ≥ 3 of weight loss, low physical activity, exhaustion, weak grip strength, and slow walking time. Independent predictors of frailty were evaluated using multivariable logistic regression.
The mean ages of the HIV-infected and HIV-seronegative groups were 41.1 ± 7.9 years and 42.6 ± 9.6 years, respectively. Of the HIV-infected adults, 87.1% were receiving antiretroviral treatment (median duration, 58 months), their median CD4 count was 468 cells/μL (interquartile range = 325-607 cells/μL) and 84.3% had undetectable plasma viral load. HIV-infected adults were more likely to be frail than HIV-seronegative individuals (19.4% vs. 13.3%; P = 0.07), and this association persisted after adjustment for confounding variables [adjusted OR = 2.14; 95% confidence interval (95% CI): 1.16-3.92, P = 0.01]. Among HIV-infected individuals, older age was a strong predictor of frailty, especially among women (women: OR = 2.55 per 10-year age increase; men: OR = 1.29 per 10-year age increase, P-interaction = 0.01). Lower current CD4 count (<500 cells/μL) was also independently associated with frailty (OR = 2.84; 95% CI: 1.02 -7.92, P = 0.04).
HIV infection is associated with premature development of frailty, especially in women. Since higher CD4 counts were associated with lower risk of frailty, earlier initiation of antiretroviral treatment may be protective.
有证据表明,HIV 感染与过早衰弱有关——衰弱通常被视为与衰老有关的综合征。我们在南非的 HIV 感染者人群中确定了衰弱的患病率和预测因素。
对 504 名年龄在 30 岁以上的成年人进行病例对照研究,其中包括 248 名 HIV 感染者和 256 名年龄和性别匹配、频数匹配的 HIV 血清阴性个体。
衰弱通过包含体重减轻、体力活动减少、疲惫、握力弱和步行速度慢等≥3 项标准评估来定义。使用多变量逻辑回归评估衰弱的独立预测因素。
HIV 感染者和 HIV 血清阴性组的平均年龄分别为 41.1±7.9 岁和 42.6±9.6 岁。在 HIV 感染者中,87.1%正在接受抗逆转录病毒治疗(中位数持续时间为 58 个月),其 CD4 计数中位数为 468 个/μL(四分位距为 325-607 个/μL),84.3%的患者血浆病毒载量不可检测。与 HIV 血清阴性个体相比,HIV 感染者更容易衰弱(19.4%比 13.3%;P=0.07),并且在调整混杂变量后这种关联仍然存在[调整后的 OR=2.14;95%置信区间(95%CI):1.16-3.92,P=0.01]。在 HIV 感染者中,年龄较大是衰弱的强烈预测因素,尤其是女性(女性:每增加 10 岁,OR=2.55;男性:每增加 10 岁,OR=1.29,P 交互=0.01)。目前较低的 CD4 计数(<500 个/μL)也与衰弱独立相关(OR=2.84;95%CI:1.02-7.92,P=0.04)。
HIV 感染与衰弱的过早发生有关,尤其是在女性中。由于较高的 CD4 计数与衰弱风险较低有关,因此早期开始抗逆转录病毒治疗可能具有保护作用。