Palmieri Vittorio, Arnett Donna K, Roman Mary J, Liu Jennifer E, Bella Jonathan N, Oberman Albert, Kitzman Dalane W, Hopkins Paul N, Morgan Derek, de Simone Giovanni, Devereux Richard B
Weill Medical College of Cornell University, New York, New York 10021, USA.
Am J Med. 2002 Jun 15;112(9):710-5. doi: 10.1016/s0002-9343(02)01123-3.
Previous studies of the association between the use of appetite suppressants and valvular heart disease have not accounted for the effects of valvular structure and aortic root diameter, which are associated with obesity. We assessed whether the use of the appetite suppressants fenfluramine/dexfenfluramine, either alone or with phentermine, was associated with aortic regurgitation while adjusting for these variables.
The sample included 2524 adult participants in the population-based Hypertension Genetic Epidemiology Network study. Information regarding current drug use was assessed during a clinical examination. Medication use was continued at the time of echocardiographic study. Expert readers blinded to current therapy read echocardiograms centrally at Cornell Medical Center. Analyses of the associations between use of fenfluramine/dexfenfluramine (alone or with phentermine) and aortic regurgitation adjusted for potential confounders, including aortic root dilatation and valve fibrocalcification.
Nineteen participants, all of whom had hypertension, were being treated with fenfluramine or dexfenfluramine (5 on these agents alone, 14 also with phentermine). Aortic regurgitation was present in 32% (n = 6) of those taking fenfluramine or dexfenfluramine versus 6% (162/2505) of remaining subjects (P = 0.001). In multivariate-adjusted analyses, treatment with fenfluramine or dexfenfluramine was associated with aortic regurgitation (odds ratio [OR] = 4.9; 95% confidence interval [CI]: 1.7 to 14) and aortic fibrocalcification (OR = 5.2; 95% CI: 1.9 to 15).
In a population-based sample, use of fenfluramine or dexfenfluramine, alone or in combination with phentermine, was associated with aortic regurgitation independent of aortic dilatation or fibrocalcification.
以往关于食欲抑制剂与心脏瓣膜病之间关联的研究未考虑与肥胖相关的瓣膜结构和主动脉根部直径的影响。我们在对这些变量进行校正的同时,评估单独使用食欲抑制剂芬氟拉明/右芬氟拉明或与苯丁胺联用是否与主动脉瓣反流有关。
样本包括基于人群的高血压遗传流行病学网络研究中的2524名成年参与者。在临床检查期间评估当前用药信息。在进行超声心动图检查时继续用药。对当前治疗不知情的专业阅片者在康奈尔医学中心集中阅读超声心动图。分析芬氟拉明/右芬氟拉明(单独或与苯丁胺联用)的使用与主动脉瓣反流之间的关联,并对包括主动脉根部扩张和瓣膜纤维钙化在内的潜在混杂因素进行校正。
19名参与者正在接受芬氟拉明或右芬氟拉明治疗,他们均患有高血压(5名仅使用这些药物,14名还联用苯丁胺)。服用芬氟拉明或右芬氟拉明的参与者中32%(n = 6)存在主动脉瓣反流,而其余受试者中这一比例为6%(162/2505)(P = 0.001)。在多变量校正分析中,芬氟拉明或右芬氟拉明治疗与主动脉瓣反流(比值比[OR] = 4.9;95%置信区间[CI]:1.7至l4)和主动脉纤维钙化(OR = 5.2;95%CI:1.9至15)相关。
在基于人群的样本中,单独使用或与苯丁胺联用芬氟拉明或右芬氟拉明与主动脉瓣反流有关,且独立于主动脉扩张或纤维钙化。