Torpey Kwasi, Ganu Vincent, Kenu Ernest, Ayisi Addo Stephen, Agyabeng Kofi, Odikro Magdalene Akos, Adu-Gyamfi Raphael, Mohammed Abdul Gafaru, Lartey Margaret
Department of Population, Family, Reproductive Health, School of Public health, University of Ghana, Accra, Ghana.
Department of Medicine, Korle Bu Teaching Hospital, Accra, Ghana
BMJ Open. 2025 May 8;15(5):e097340. doi: 10.1136/bmjopen-2024-097340.
The use of antiretroviral therapy has been linked to the development of some components of metabolic syndrome (MetS), specifically glucose intolerance, weight gain and defective lipid metabolism. This study determined the relationship between dolutegravir (DTG) and MetS in a cohort of persons living with HIV (PWH) initiating DTG-based regimen in Ghana.
A 2-year observational prospective study was conducted from September 2020 to August 2022.
Five HIV high-burden facilities providing antiretroviral therapy services at the district and tertiary levels of care in Ghana.
Persons with HIV who were newly enrolled onto DTG.
Waist circumference, body mass index, blood pressure, fasting blood glucose and lipids were the primary outcomes measured at baseline, 3, 6, 12 and at 18 months follow-up to determine the incidence of MetS. MetS was defined using the Joint Consensus definition that combines the International Diabetes Federation and the National Cholesterol Education Programme Adult Treatment Panel III (ATP III) definitions. The Kaplan-Meier estimator was used to estimate the risk of developing MetS. The Cox proportional hazard model was used in estimating HRs.
Of 3664 PWH screened at baseline, 31.4% (1152/3664) had MetS. Of the remaining 2512 with no MetS at baseline, there were 960 incident cases of MetS over the 1.5 years follow-up. The estimated MetS incident rate is 384.2 (95% CI: 360.6 to 409.2) per 1000 person-years with a median time to development of MetS at 6 months (IQR; 3-12 months). Being female (adjsuted HR, aHR: 1.42, 95% CI: 1.19 to 1.70), age ≥50 years (aHR: 1.30, 95% CI: 1.12 to 1.51), having a comorbidity at baseline (aHR: 1.39, 95% CI: 1.12 to 1.51) and being overweight (aHR: 1.46, 95% CI: 1.25 to 1.71) and obese (aHR: 1.62, 95% CI: 1.36 to 1.93) were associated with higher risk of MetS development.
The incidence of MetS was high among our patients, with elevated fasting blood sugar and elevated blood pressure being the most common developed MetS defining components. HIV programmes should institute targeted interventions at addressing central obesity to reduce the risk of MetS.
抗逆转录病毒疗法的使用与代谢综合征(MetS)某些组成部分的发展有关,特别是葡萄糖不耐受、体重增加和脂质代谢缺陷。本研究确定了在加纳开始基于多替拉韦(DTG)方案治疗的人类免疫缺陷病毒(HIV)感染者队列中,DTG与MetS之间的关系。
2020年9月至2022年8月进行了一项为期2年的观察性前瞻性研究。
加纳五个在地区和三级护理层面提供抗逆转录病毒治疗服务的HIV高负担机构。
新开始使用DTG的HIV感染者。
腰围、体重指数、血压、空腹血糖和血脂是在基线、3个月、6个月、12个月和18个月随访时测量的主要结局指标,以确定MetS的发病率。MetS采用结合国际糖尿病联盟和美国国家胆固醇教育计划成人治疗小组III(ATP III)定义的联合共识定义。采用Kaplan-Meier估计器估计发生MetS的风险。采用Cox比例风险模型估计风险比(HRs)。
在基线筛查的3664名HIV感染者中,31.4%(1152/3664)患有MetS。在基线时其余2512名无MetS的患者中,在1.5年的随访中有960例MetS新发病例。估计MetS发病率为每1000人年384.2(95%CI:360.6至409.2),发生MetS的中位时间为6个月(IQR;3 - 12个月)。女性(调整后HR,aHR:1.42,95%CI:1.19至1.70)、年龄≥50岁(aHR:1.30,95%CI:1.12至1.51)、基线时患有合并症(aHR:1.39,95%CI:1.12至1.51)、超重(aHR:1.46,95%CI:1.25至1.71)和肥胖(aHR:1.62,95%CI:1.36至1.93)与发生MetS的较高风险相关。
我们的患者中MetS发病率较高,空腹血糖升高和血压升高是最常见的已发生的MetS定义成分。HIV项目应制定针对性干预措施以解决中心性肥胖问题,降低MetS风险。