Serfaty-Lacrosniere C, Civeira F, Lanzberg A, Isaia P, Berg J, Janus E D, Smith M P, Pritchard P H, Frohlich J, Lees R S
Lipid Research Laboratory, Endocrinology Division, New England Medical Center, MA.
Atherosclerosis. 1994 May;107(1):85-98. doi: 10.1016/0021-9150(94)90144-9.
Decreased levels of plasma high density lipoprotein (HDL) cholesterol have been associated with premature cardiovascular disease (CVD). Tangier disease is an autosomal co-dominant disorder in which homozygotes have a marked deficiency of HDL cholesterol and apolipoprotein (apo) A-I levels (both < 10 mg/dl), decreased low density lipoprotein (LDL) cholesterol levels (about 40% of normal), and mild hypertriglyceridemia. Homozygotes develop cholesterol ester deposition in tonsils (orange tonsils), liver, spleen, gastrointestinal tract, lymph nodes, bone marrow, and Schwann cells. Our purpose was to assess the prevalence of CVD in Tangier disease. We reviewed published clinical information on 51 cases of homozygous Tangier disease, report 3 new cases and provide autopsy information on 3 cases. Mean (+/- S.D.) lipid values of all cases were as follows: total cholesterol 68 +/- 30 mg/dl (32% of normal), triglycerides 201 +/- 118 mg/dl (162% of normal), HDL cholesterol 3 +/- 3 mg/dl (6% of normal) and LDL cholesterol 50 +/- 38 mg/dl (37% of normal). The most common clinical finding in these subjects (n = 54) was peripheral neuropathy which was observed in 54% of cases versus < 1% of control subjects (n = 3130). CVD was observed in 20% of Tangier patients versus 5% of controls (P < 0.05), and in those that were between 35 and 65 years of age, 44% (11 of 25) had evidence of CVD (either angina, myocardial infarction or stroke) versus 6.5% in 1533 male controls and 3.2% in 1597 female controls in this age group (P < 0.01). In 9 patients who died, 2 died prior to age 20 of probable infectious diseases, 3 of documented coronary heart disease at ages 48, 64, and 72, 2 of stroke at ages 56 and 69, one of valvular heart disease, and 1 of cancer. In three autopsy cases, significant diffuse atherosclerosis was observed in one at age 64, moderate atherosclerosis and cerebral infarction in another at age 56, but no atherosclerosis was noted in the third case who died of lymphoma at age 62. In one patient with established coronary heart disease, none of the lipid lowering agents used (niacin, gemfibrozil, estrogen or lovastatin) raised HDL cholesterol levels above 5 mg/dl. However, these agents did have significant effects on lowering triglyceride and LDL cholesterol levels. Our data indicate that there may be heterogeneity in these patients with regard to CVD risk, that peripheral neuropathy is a major problem in many patients, and that CVD is a significant clinical problem in middle aged and elderly Tangier homozygotes.(ABSTRACT TRUNCATED AT 400 WORDS)
血浆高密度脂蛋白(HDL)胆固醇水平降低与心血管疾病(CVD)的过早发生有关。丹吉尔病是一种常染色体共显性疾病,纯合子患者的HDL胆固醇和载脂蛋白(apo)A-I水平显著缺乏(均<10mg/dl),低密度脂蛋白(LDL)胆固醇水平降低(约为正常水平的40%),伴有轻度高甘油三酯血症。纯合子患者在扁桃体(橙色扁桃体)、肝脏、脾脏、胃肠道、淋巴结、骨髓和施万细胞中出现胆固醇酯沉积。我们的目的是评估丹吉尔病患者中CVD的患病率。我们回顾了已发表的51例纯合子丹吉尔病的临床信息,报告了3例新病例,并提供了3例尸检信息。所有病例的平均(±标准差)血脂值如下:总胆固醇68±30mg/dl(为正常水平的32%),甘油三酯201±118mg/dl(为正常水平的162%),HDL胆固醇3±3mg/dl(为正常水平的6%),LDL胆固醇50±38mg/dl(为正常水平的37%)。这些受试者(n = 54)中最常见的临床发现是周围神经病变,54%的病例出现该病变,而对照受试者(n = 3130)中这一比例<1%。20%的丹吉尔病患者出现CVD,而对照组为5%(P<0.05);在年龄在35至65岁之间的患者中,44%(25例中的11例)有CVD证据(心绞痛、心肌梗死或中风),而该年龄组的1533名男性对照者中这一比例为6.5%,1597名女性对照者中为3.2%(P<0.01)。在9例死亡患者中,2例在20岁之前死于可能的传染病,3例分别在48岁、64岁和72岁时死于确诊的冠心病,2例分别在56岁和69岁时死于中风,1例死于瓣膜性心脏病,1例死于癌症。在3例尸检病例中,1例64岁患者出现显著的弥漫性动脉粥样硬化,另1例56岁患者出现中度动脉粥样硬化和脑梗死,但第3例62岁死于淋巴瘤的患者未发现动脉粥样硬化。在1例确诊为冠心病的患者中,使用的降脂药物(烟酸、吉非贝齐、雌激素或洛伐他汀)均未使HDL胆固醇水平升高至5mg/dl以上。然而,这些药物确实对降低甘油三酯和LDL胆固醇水平有显著作用。我们的数据表明,这些患者在CVD风险方面可能存在异质性,周围神经病变是许多患者的主要问题,CVD是中年和老年丹吉尔病纯合子患者的一个重要临床问题。(摘要截断于400字)