Kazibwe Richard, Jehopio Jeshuah, Schaich Christopher L, Rikhi Rishi, Mirzai Saeid, Chevli Parag A, Namutebi Juliana H, Chebrolu Sneha, O'Connor Shannon, Yeboah Joseph, Shapiro Michael D
Department of Internal Medicine, Wake Forest University School of Medicine, 1 Medical Center Medical Center Boulevard, Winston-Salem, NC 27157, USA.
Uganda Christian University, School of Medicine, P.O. Box 4, Mukono, Uganda.
Prog Cardiovasc Dis. 2025 May 18. doi: 10.1016/j.pcad.2025.05.006.
Atherogenic dyslipidemia (AD), characterized by low high-density lipoprotein cholesterol (HDL-C) and elevated triglycerides (TG), is associated with increased cardiovascular disease (CVD) risk. This study evaluates the association between AD and CVD in hypertension treated to systolic blood pressure (SBP) targets of <120 mmHg (intensive) or < 140 mmHg (standard).
We included 9361 participants from the Systolic Blood Pressure Intervention Trial (SPRINT). Based on baseline lipid profiles, low HDL-C was defined as <40 mg/dL in men or < 50 mg/dL in women, and high TG as ≥150 mg/dL. Participants were classified into four lipid categories according to these cutoffs. AD was defined as the combination of low HDL-C and high TG. We used multivariable Cox regression to evaluate the association between lipid categories and the primary SPRINT outcome, a composite of major CVD events.
Over a median 3.8-year follow-up, 726 primary outcome events occurred. The incidence of the primary outcome was 9.5% (n = 104) in those with AD and 7.4% (n = 434) with normal HDL-C and TG. Compared to the reference group (normal HDL-C with normal TG), the hazard ratios (HRs) for primary outcome were 1.07 (95 % CI: 0.85-1.35) for high TG alone, 1.20 (95 % CI: 0.95-1.52) for low HDL-C alone, and 1.41 (95 % CI: 1.12-1.77) for AD. Similarly, HRs for the primary outcome associated with AD were 1.38 (95 % CI: 1.02-1.87) and 1.44 (95 % CI: 1.01-2.05) in the standard and intensive SBP-lowering arms, respectively.
Among SPRINT participants, AD was associated with a higher CVD risk. Early detection of AD in hypertensive patients, even without diabetes, may prompt greater therapeutic effort to reduce long-term CVD risk.
致动脉粥样硬化性血脂异常(AD)以高密度脂蛋白胆固醇(HDL-C)降低和甘油三酯(TG)升高为特征,与心血管疾病(CVD)风险增加相关。本研究评估了在收缩压(SBP)目标为<120 mmHg(强化治疗)或<140 mmHg(标准治疗)的高血压患者中,AD与CVD之间的关联。
我们纳入了收缩压干预试验(SPRINT)的9361名参与者。根据基线血脂谱,男性HDL-C<40 mg/dL或女性HDL-C<50 mg/dL定义为HDL-C降低,TG≥150mg/dL定义为TG升高。根据这些切点将参与者分为四类血脂情况。AD定义为HDL-C降低和TG升高同时存在。我们使用多变量Cox回归来评估血脂类别与SPRINT主要结局(主要CVD事件的复合结局)之间的关联。
在中位3.8年的随访期间,发生了726例主要结局事件。AD患者的主要结局发生率为9.5%(n = 104),HDL-C和TG正常的患者为7.4%(n = 434)。与参照组(HDL-C和TG均正常)相比,单纯TG升高时主要结局的风险比(HR)为1.07(95%CI:0.85-1.35),单纯HDL-C降低时为1.20(95%CI:0.95-1.52),AD时为1.41(95%CI:1.12-1.77)。同样,在标准降压组和强化降压组中,与AD相关的主要结局的HR分别为1.38(95%CI:1.02-1.87)和1.44(95%CI:1.01-2.05)。
在SPRINT参与者中,AD与更高的CVD风险相关。即使在无糖尿病的高血压患者中,早期检测出AD可能会促使加大治疗力度以降低长期CVD风险。