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家族性无β脂蛋白血症中活化因子VII极低及因子VII抗原减少。

Very low activated factor VII and reduced factor VII antigen in familial abetalipoproteinaemia.

作者信息

Miller G J, Mitropoulos K A, Nanjee M N, Howarth D J, Martin J C, Esnouf M P, Reeves B E, Miller N E, Cooper J A

机构信息

Medical Research Council Epidemiology and Medical Care Unit, London, England.

出版信息

Thromb Haemost. 1998 Aug;80(2):233-8.

PMID:9716144
Abstract

Abetalipoproteinaemia is a rare disorder of apolipoprotein B metabolism associated with extremely low plasma concentrations of triglyceride. To discover whether the general positive association between factor VII and triglyceride levels extends to this condition, 5 patients were compared with 18 controls. All patients had a triglyceride below 100 micromol/l. Plasma unesterified fatty acid concentration was normal. Although factor IX activity was only slightly reduced (mean 88% standard) and factor IX antigen was normal, mean activated factor VII in patients was strikingly reduced to 34% of that in controls, a level similar to that found in haemophilia B. The patients' mean factor VII activity and factor VII antigen were also significantly reduced to 54% and 63% of those in controls, respectively. Mean factor XI activity and tissue factor pathway inhibitor activity were reduced in patients to 70% and 75% of control values respectively, while factor XII, factor XI antigen, factor X, prothrombin and protein C were normal.

摘要

无β脂蛋白血症是一种罕见的载脂蛋白B代谢紊乱疾病,与极低的血浆甘油三酯浓度相关。为了探究因子VII与甘油三酯水平之间普遍存在的正相关关系是否也适用于这种情况,对5名患者和18名对照者进行了比较。所有患者的甘油三酯水平均低于100微摩尔/升。血浆未酯化脂肪酸浓度正常。尽管因子IX活性仅略有降低(平均为标准值的88%)且因子IX抗原正常,但患者的平均活化因子VII显著降低至对照者的34%,这一水平与乙型血友病患者相似。患者的平均因子VII活性和因子VII抗原也分别显著降低至对照者的54%和63%。患者的平均因子XI活性和组织因子途径抑制物活性分别降至对照值的70%和75%,而因子 XII、因子XI抗原、因子X、凝血酶原和蛋白C均正常。

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