Suppr超能文献

进行性家族性肝内胆汁淤积症:部分胆汁转流可使非肝硬化患者的血脂正常化并促进生长。

Progressive familial intrahepatic cholestasis: partial biliary diversion normalizes serum lipids and improves growth in noncirrhotic patients.

作者信息

Melter M, Rodeck B, Kardorff R, Hoyer P F, Petersen C, Ballauff A, Brodehl J

机构信息

Department of Pediatric Nephrology and Metabolic Disorders, Children's Hospital, Hannover Medical School, Germany.

出版信息

Am J Gastroenterol. 2000 Dec;95(12):3522-8. doi: 10.1111/j.1572-0241.2000.03370.x.

Abstract

OBJECTIVES

Progressive familial intrahepatic cholestasis (PFIC) usually presents with pruritus, jaundice, hepatomegaly, and growth failure. A group of PFIC is recognized by marked elevation of total serum bile acids, decreased serum apolipoprotein A-1, and high-density lipoprotein, but normal gamma-glutamyltranspeptidase and cholesterol. Although medical therapy generally fails, partial external biliary diversion (DIV) has been used with promising results for cholestasis. However, little has been reported of its effect on linear growth, synthetic liver function, and lipid metabolism.

METHODS

DIV was performed on six noncirrhotic children with PFIC, all suffering from severe pruritus and cholestasis, refractory to medical treatment. Stature was below -1 (median, -2.3) standard deviation score (SDS) for height in all cases. All patients had markedly enhanced bile acids (307 +/- 72 microl/L), markedly decreased high-density lipoprotein (20 +/- 7 mg/dl), and apolipoprotein A-1 (58 +/- 37 mg/dl), but normal gamma-glutamyltranspeptidase and cholesterol. In addition, cholinesterase activity, monoethylglycinexylidide test, and Fischer's ratio indicated a significantly reduced synthetic liver function in all children but the youngest.

RESULTS

After DIV, all patients were consistently relieved of pruritus, and experienced normalization of all liver function tests, including cholinesterase activity, monoethylglycinexylidide test, and Fischer's ratio, as well as the serum lipid profile within 1 yr. In addition, a marked catch-up growth (median, +/- 1.3 SDS) was evident after 1 yr in all cases.

CONCLUSIONS

This report shows an excellent result of DIV in noncirrhotic PFIC patients and compares favorably with other reports. All patients experienced complete remission, including normalization of synthetic liver function and lipid metabolism. For the first time we have shown that DIV can also be associated with an accelerated growth in these patients.

摘要

目的

进行性家族性肝内胆汁淤积症(PFIC)通常表现为瘙痒、黄疸、肝肿大和生长发育迟缓。一组PFIC患者表现为血清总胆汁酸显著升高、血清载脂蛋白A-1和高密度脂蛋白降低,但γ-谷氨酰转肽酶和胆固醇正常。尽管药物治疗通常无效,但部分外引流术(DIV)已用于治疗胆汁淤积症并取得了有希望的结果。然而,关于其对线性生长、肝脏合成功能和脂质代谢的影响报道较少。

方法

对6例非肝硬化的PFIC患儿进行DIV,所有患儿均有严重瘙痒和胆汁淤积,药物治疗无效。所有病例的身高均低于身高标准差评分(SDS)-1(中位数,-2.3)。所有患者的胆汁酸均显著升高(307±72微升/升),高密度脂蛋白(20±7毫克/分升)和载脂蛋白A-1(58±37毫克/分升)显著降低,但γ-谷氨酰转肽酶和胆固醇正常。此外,胆碱酯酶活性、单乙基甘氨酰二甲苯胺试验和Fischer比值表明,除最年幼的患儿外,所有患儿的肝脏合成功能均显著降低。

结果

DIV术后,所有患者的瘙痒症状持续缓解,所有肝功能指标,包括胆碱酯酶活性、单乙基甘氨酰二甲苯胺试验和Fischer比值以及血清脂质谱在1年内均恢复正常。此外,所有病例在1年后均出现明显的追赶生长(中位数,±1.3 SDS)。

结论

本报告显示DIV在非肝硬化PFIC患者中取得了优异的效果,与其他报告相比具有优势。所有患者均完全缓解,包括肝脏合成功能和脂质代谢正常化。我们首次表明,DIV还可使这些患者加速生长。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验