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沃纳综合征中可遗传的异常脂蛋白代谢,类似于家族性高胆固醇血症。

Inheritable abnormal lipoprotein metabolism in Werner's syndrome similar to familial hypercholesterolaemia.

作者信息

Mori S, Yokote K, Morisaki N, Saito Y, Yoshida S

机构信息

Second Department of Internal Medicine, School of Medicine, Chiba University, Japan.

出版信息

Eur J Clin Invest. 1990 Apr;20(2):137-42. doi: 10.1111/j.1365-2362.1990.tb02260.x.

DOI:10.1111/j.1365-2362.1990.tb02260.x
PMID:2112477
Abstract

Studies were made on the abnormality of lipoprotein metabolism and its cause in 10 patients with Werner's syndrome. Seven of the 10 patients had hypercholesterolaemia (above 250 mg dl-1). Six of the seven patients with hypercholesterolaemia had thickened Achilles' tendons (greater than 9 mm). A significant positive correlation (P less than 0.01) was found between the serum total cholesterol levels and the thickness of Achilles' tendons in these 10 patients, suggesting that the substance precipitated in the thickened tendons is derived from serum cholesterol. Some first-degree relatives of three patients with both hypercholesterolaemia and xanthoma-like thickening of Achilles' tendons also suffered from hypercholesterolaemia. Moreover, the low density lipoprotein (LDL) receptor activities in peripheral lymphocytes of five patients with both hypercholesterolaemia and xanthoma-like tendons were significantly (P less than 0.001) lower than those of controls, whereas the LDL receptor activities of two patients without hypercholesterolaemia were almost the same as those of controls. These findings suggest that, at least these five patients with lower lymphocyte LDL receptor activities, and probably another patient with both hypercholesterolaemia and xanthoma-like thickening of Achilles' tendons suffered from familial hypercholesterolaemia (FH). If this is the case, this high frequency of association of Werner's syndrome with FH (in six of 10 patients) suggests some relationship between these two diseases.

摘要

对10例沃纳综合征患者的脂蛋白代谢异常及其病因进行了研究。10例患者中有7例患有高胆固醇血症(高于250mg/dl)。7例高胆固醇血症患者中有6例跟腱增厚(大于9mm)。在这10例患者中,血清总胆固醇水平与跟腱厚度之间存在显著正相关(P<0.01),这表明在增厚的肌腱中沉淀的物质来源于血清胆固醇。3例同时患有高胆固醇血症和跟腱黄瘤样增厚的患者的一些一级亲属也患有高胆固醇血症。此外,5例同时患有高胆固醇血症和肌腱黄瘤样病变的患者外周淋巴细胞中的低密度脂蛋白(LDL)受体活性显著低于对照组(P<0.001),而2例无高胆固醇血症患者的LDL受体活性与对照组几乎相同。这些发现表明,至少这5例淋巴细胞LDL受体活性较低的患者,可能还有另1例同时患有高胆固醇血症和跟腱黄瘤样增厚的患者患有家族性高胆固醇血症(FH)。如果是这样,沃纳综合征与FH的这种高关联频率(10例患者中有6例)表明这两种疾病之间存在某种关系。

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Inheritable abnormal lipoprotein metabolism in Werner's syndrome similar to familial hypercholesterolaemia.沃纳综合征中可遗传的异常脂蛋白代谢,类似于家族性高胆固醇血症。
Eur J Clin Invest. 1990 Apr;20(2):137-42. doi: 10.1111/j.1365-2362.1990.tb02260.x.
2
[Hyperlipidemia as a complication of patients with Werner's syndrome].[高脂血症作为沃纳综合征患者的一种并发症]
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Serum lipoprotein and lymphocyte LDL receptor studies in parents and children with heterozygous familial hypercholesterolaemia.杂合子家族性高胆固醇血症患者及其父母的血清脂蛋白和淋巴细胞低密度脂蛋白受体研究。
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Lipid and lipoprotein parameters for detection of familial hypercholesterolemia in childhood. The DECOPIN Project.用于检测儿童家族性高胆固醇血症的脂质和脂蛋白参数。DECOPIN项目。
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Achilles tendon thickness in hypercholesterolaemia.高胆固醇血症患者的跟腱厚度
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Pathogenesis, detection and treatment of Achilles tendon xanthomas.跟腱黄瘤的发病机制、检测与治疗
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Articular manifestations of familial hypercholesterolaemia.家族性高胆固醇血症的关节表现。
Ann Rheum Dis. 1985 Sep;44(9):599-602. doi: 10.1136/ard.44.9.599.

引用本文的文献

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Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice.产生沃纳综合征解旋酶突变蛋白的小鼠与Wrn基因敲除小鼠之间的代谢和表型差异。
PLoS One. 2015 Oct 8;10(10):e0140292. doi: 10.1371/journal.pone.0140292. eCollection 2015.
2
Potential for pharmacological intervention in Werner syndrome.沃纳综合征的药物干预潜力。
Drugs Aging. 1995 Dec;7(6):449-58. doi: 10.2165/00002512-199507060-00005.
3
Role of phospholipase A2 in expression of the scavenger pathway in cultured aortic smooth muscle cells stimulated with phorbol 12-myristate 13-acetate.
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Biochem J. 1994 Oct 1;303 ( Pt 1)(Pt 1):247-53. doi: 10.1042/bj3030247.