Dirajlal-Fargo Sahera, Webel Allison R, Longenecker Chris T, Kinley Bruce, Labbato Danielle, Sattar Abdus, McComsey Grace A
Case Western Reserve University, Cleveland, OH, USA.
Antivir Ther. 2016;21(3):237-45. doi: 10.3851/IMP2998. Epub 2015 Oct 12.
In HIV-uninfected populations, physical activity decreases mortality and inflammation. Inflammation is a potential cause of comorbidities in HIV+ adults, the evidence examining the effect of physical activity on cardiometabolic health is limited. This analysis examines the relationship between physical activity, cardiometabolic health and inflammation.
We conducted a nested study within the SATURN-HIV trial in which 147 HIV+ adults were randomized to 10 mg daily rosuvastatin or placebo. Measures of physical activity, cardiometabolic health, inflammation and vascular disease (carotid artery intima media thickness and computed tomography-acquired measures pericardial fat volume) were assessed at baseline and through 96 weeks. Spearman correlations and multivariable analyses were used to explore relationships between physical activity, cardiometabolic health and inflammation.
Median age (Q1, Q3) was 46 (40.4, 52.7) years, 80% were male, 69% were African American and 46% were on protease inhibitors. Baseline median physical activity was 44 min per week (0, 150), 24% of participants performed greater than 150 min per week. At baseline, physical activity correlated with several markers of cardiometabolic health and inflammation (all P≤0.05). Over all time points median physical activity was independently associated with carotid distensibility (β=2.53; P=0.008), pericardial fat volume (β=-6.13; P=0.001) and interleukin-6 (β=-0.468; P<0.001).
Physical activity is associated with vascular disease, endothelial function, and may be an adjuvant to decreasing comorbidities in HIV+ adults. Further studies should examine long-term effects of physical activity on cardiometabolic health and inflammation in this population. Clinicaltrials.gov NCT01218802.
在未感染艾滋病毒的人群中,体育活动可降低死亡率和炎症水平。炎症是艾滋病毒阳性成年人合并症的一个潜在原因,而关于体育活动对心脏代谢健康影响的证据有限。本分析旨在研究体育活动、心脏代谢健康与炎症之间的关系。
我们在SATURN-HIV试验中进行了一项嵌套研究,将147名艾滋病毒阳性成年人随机分为每日服用10毫克瑞舒伐他汀组或安慰剂组。在基线和96周期间评估体育活动、心脏代谢健康、炎症和血管疾病(颈动脉内膜中层厚度和计算机断层扫描测量的心包脂肪体积)指标。采用Spearman相关性分析和多变量分析来探讨体育活动、心脏代谢健康与炎症之间的关系。
年龄中位数(四分位间距)为46(40.4,52.7)岁,80%为男性,69%为非裔美国人,46%正在使用蛋白酶抑制剂。基线时体育活动中位数为每周44分钟(0,150),24%的参与者每周体育活动时间超过150分钟。在基线时,体育活动与心脏代谢健康和炎症的多个指标相关(所有P≤0.05)。在所有时间点,体育活动中位数与颈动脉扩张性(β=2.53;P=0.008)、心包脂肪体积(β=-6.13;P=0.001)和白细胞介素-6(β=-0.468;P<0.001)独立相关。
体育活动与血管疾病、内皮功能相关,可能是降低艾滋病毒阳性成年人合并症的辅助手段。进一步的研究应考察体育活动对该人群心脏代谢健康和炎症的长期影响。Clinicaltrials.gov NCT01218802。