Weill Cornell Medicine, Department of Medicine, New York, New York, USA.
Groupe Haitien d'Etude du Sarcome de Kaposi et des Infections Opportunistes (GHESKIO), Port-au-Prince, Haiti.
J Hypertens. 2018 Jul;36(7):1533-1539. doi: 10.1097/HJH.0000000000001723.
The objective of this study was to determine how baseline blood pressure and incident hypertension related to antiretroviral therapy (ART) initiation, HIV-related inflammation and mortality in HIV-infected adults in a low-income country.
We conducted long-term follow-up of HIV-infected adults who had participated in a trial of early vs. delayed initiation of ART in Port-au-Prince, Haiti. Between 2005 and 2008, 816 HIV-infected adults were randomized to early (N = 408) vs. delayed ART (when CD4 cell count <200 cells/μl or AIDS-defining condition; N = 408). Blood pressure was measured every 3 months. Hypertension was diagnosed according to the Joint National Committee (JNC-7) guidelines. Biomarkers of inflammation and coagulation were measured from banked enrolment plasma samples. Survival analyses were performed using Stata 14.
The median age at enrolment was 39 years. The median follow-up time was 7.3 years. The hypertension incidence rate was 3.41 per 100 person-years, and was similar in early and delayed ART groups. In multivariable models, independent predictors of incident hypertension were older age, higher BMI and plasma interleukin (IL)-6 levels (adjusted hazard ratio, aHR = 1.23, P < 0.001). Systolic pressure more than 140 mmHg at enrolment was associated with increased mortality (aHR = 2.47, P = 0.03) as was systolic pressure less than 90 mmHg (aHR = 2.25, P = 0.04). Prevalent and incident hypertension were also significantly associated with mortality.
In a large prospective study of HIV-infected adults, we found a high incidence of hypertension associated with HIV-related inflammation. Baseline hypertension conferred a more than two-fold increased risk of death. Among HIV-infected adults in low-income countries, hypertension should be considered a serious threat to long-term survival.
本研究旨在确定基线血压和新发高血压与抗逆转录病毒治疗(ART)的启动、HIV 相关炎症和低收入国家 HIV 感染成年人死亡率之间的关系。
我们对参加海地太子港早期与延迟启动 ART 试验的 HIV 感染成年人进行了长期随访。在 2005 年至 2008 年期间,816 名 HIV 感染成年人被随机分为早期(N=408)与延迟 ART(当 CD4 细胞计数<200 个/μl 或出现 AIDS 定义性疾病时;N=408)组。每 3 个月测量一次血压。高血压的诊断依据是联合国家委员会(JNC-7)指南。从已保存的入组血浆样本中测量炎症和凝血的生物标志物。使用 Stata 14 进行生存分析。
入组时的中位年龄为 39 岁。中位随访时间为 7.3 年。高血压发病率为每 100 人年 3.41 例,早期和延迟 ART 组相似。在多变量模型中,新发高血压的独立预测因素为年龄较大、BMI 较高和血浆白细胞介素(IL)-6 水平较高(调整后的危险比,aHR=1.23,P<0.001)。入组时收缩压超过 140mmHg 与死亡率增加相关(aHR=2.47,P=0.03),收缩压低于 90mmHg 也与死亡率增加相关(aHR=2.25,P=0.04)。已确诊和新发高血压与死亡率也显著相关。
在一项对 HIV 感染成年人的大型前瞻性研究中,我们发现与 HIV 相关炎症相关的高血压发病率很高。基线高血压使死亡风险增加两倍以上。在低收入国家的 HIV 感染成年人中,高血压应被视为对长期生存的严重威胁。