Schaefer Ernst J, Anthanont Pimjai, Diffenderfer Margaret R, Polisecki Eliana, Asztalos Bela F
Cardiovascular Nutrition Laboratory, Human Nutrition Research Center on Aging at Tufts University and Tufts University School of Medicine, Boston, MA; Boston Heart Diagnostics, Framingham, MA.
Cardiovascular Nutrition Laboratory, Human Nutrition Research Center on Aging at Tufts University and Tufts University School of Medicine, Boston, MA.
Prog Cardiovasc Dis. 2016 Sep-Oct;59(2):97-106. doi: 10.1016/j.pcad.2016.08.006. Epub 2016 Aug 24.
Low serum high density lipoprotein cholesterol level (HDL-C) <40 mg/dL in men and <50 mg/dL in women is a significant independent risk factor for cardiovascular disease (CVD), and is often observed in patients with hypertriglyceridemia, obesity, insulin resistance, and diabetes. Patients with marked deficiency of HDL-C (<20 mg/dL) in the absence of secondary causes are much less common (<1% of the population). These patients may have homozygous, compound heterozygous, or heterozygous defects involving the apolipoprotein (APO)AI, ABCA1, or lecithin:cholesterol acyl transferase genes, associated with apo A-I deficiency, apoA-I variants, Tangier disease , familial lecithin:cholesteryl ester acyltransferase deficiency, and fish eye disease. There is marked variability in laboratory and clinical presentation, and DNA analysis is necessary for diagnosis. These patients can develop premature CVD, neuropathy, kidney failure, neuropathy, hepatosplenomegaly and anemia. Treatment should be directed at optimizing all non-HDL risk factors.
血清高密度脂蛋白胆固醇(HDL-C)水平低,男性<40mg/dL,女性<50mg/dL,是心血管疾病(CVD)的一个重要独立危险因素,常见于高甘油三酯血症、肥胖、胰岛素抵抗和糖尿病患者。在无继发原因的情况下,HDL-C显著缺乏(<20mg/dL)的患者较为少见(<1%的人群)。这些患者可能存在涉及载脂蛋白(APO)AI、ABCA1或卵磷脂胆固醇酰基转移酶基因的纯合、复合杂合或杂合缺陷,与载脂蛋白A-I缺乏、载脂蛋白A-I变异体、丹吉尔病、家族性卵磷脂胆固醇酯酰基转移酶缺乏症和鱼眼病相关。实验室检查和临床表现存在显著差异,诊断需要进行DNA分析。这些患者可出现过早的心血管疾病、神经病变、肾衰竭、神经病变、肝脾肿大和贫血。治疗应针对优化所有非HDL危险因素。