Masters Mary Clare, Perez Jeremiah, Tassiopoulos Katherine, Andrade Adriana, Ellis Ronald, Yang Jingyan, Brown Todd T, Palella Frank J, Erlandson Kristine M
Division of Infectious Diseases, Northwestern University, Chicago, Illinois.
Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
AIDS Res Hum Retroviruses. 2019 Nov-Dec;35(11-12):1065-1073. doi: 10.1089/AID.2019.0101. Epub 2019 Sep 30.
Gait speed declines at a faster rate in persons with HIV (PWH) than in the general population but the risk factors associated with this decline are not well understood. In the AIDS Clinical Trials Group (ACTG) A5322 (HAILO, HIV Infection, Aging, and Immune Function Long-term Observational Study), an observational cohort study of PWH ≥40 years of age, those who developed slow gait during the first 3 years of follow-up were compared with persons who maintained normal speed. Associations with demographic and clinical covariates were assessed using multivariable logistic regression. Of 929 participants, 81% were men, 31% Black, and 20% Hispanic. Median age was 51 years [interquartile range (IQR) = 46-56]. At study entry, 92% had plasma HIV RNA <50 copies/mL with median CD4 count 631 cells/mm (IQR = 458-840). At study entry, 7% of participants had slow gait, 16% had neurocognitive impairment (NCI), and 12% had diabetes. Over 3 years, 87% maintained normal gait speed, 3% maintained a slow gait, 6% developed a slow gait, and 4% improved from slow to normal gait speed. In multivariable models, hemoglobin A1C (HbA1C) percentage, per one unit increase [odds ratio (OR) = 1.36; 95% confidence interval (CI) = 1.03-1.81; = .033], NCI (OR = 3.47; 95% CI = 1.57-7.69 = .002), and black versus white race (OR = 2.45; 95% CI = 1.08-5.59; = .032) at entry were significantly associated with development of slow gait compared with those maintaining normal gait speed. The association between baseline HbA1C and development of slow gait speed highlights an intervenable target to prevent progression of physical function limitations.
与普通人群相比,HIV感染者(PWH)的步态速度下降更快,但导致这种下降的风险因素尚未完全明确。在艾滋病临床试验组(ACTG)A5322(HAILO,HIV感染、衰老和免疫功能长期观察研究)中,一项针对年龄≥40岁的PWH的观察性队列研究,将随访前3年出现步态缓慢的患者与保持正常速度的患者进行比较。使用多变量逻辑回归评估与人口统计学和临床协变量的关联。929名参与者中,81%为男性,31%为黑人,20%为西班牙裔。中位年龄为51岁[四分位间距(IQR)=46 - 56]。研究开始时,92%的患者血浆HIV RNA<50拷贝/mL,中位CD4细胞计数为631个/mm³(IQR = 458 - 840)。研究开始时,7%的参与者步态缓慢,16%有神经认知障碍(NCI),12%有糖尿病。在3年期间,87%的人保持正常步态速度,3%的人保持步态缓慢,6%的人出现步态缓慢,4%的人从步态缓慢改善为正常步态速度。在多变量模型中,与保持正常步态速度者相比,血红蛋白A1C(HbA1C)百分比每增加一个单位[比值比(OR)=1.36;95%置信区间(CI)=1.03 - 1.81;P = 0.033]、NCI(OR = 3.47;9%置信区间(CI)=1.57 - 7.69;P = 0.002)以及研究开始时黑人与白人种族(OR = 2.45;95%置信区间(CI)=1.08 - 5.59;P = 0.032)与步态缓慢的发生显著相关。基线HbA1C与步态缓慢发展之间的关联突出了一个可干预的靶点,以预防身体功能受限的进展。