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胆汁酸吸收不良患儿的粪便和胆汁胆汁酸模式

Fecal and biliary bile acid patterns in children with bile acid malabsorption.

作者信息

Tazawa Y, Yamada M, Nakagawa M, Suzuki H, Igarashi Y, Konno T, Tada K

出版信息

J Pediatr Gastroenterol Nutr. 1984 Jun;3(3):378-84. doi: 10.1097/00005176-198406000-00013.

Abstract

Bile acid metabolism was examined in two children with bile acid malabsorption, who were being treated with intravenous hyperalimentation. Fecal bile acid excretion was 1,261 mumol/m2/day in a child with bile acid malabsorption of unknown origin, and 1,877 mumol/m2/day in a child with secondary bile acid malabsorption after an operation for long-segment aganglionosis. These values were approximately 10 times higher than those in diarrheal or nondiarrheal children without apparent abnormalities in bile acid metabolism. Fecal bile acids in these patients with bile acid malabsorption were almost completely conjugated, with little unconjugated bile acid present. It is possible that the disturbed bile acid deconjugation in the intestine might be caused by a rapid intestinal transit time, which was found in our patients with bile acid malabsorption. In the analysis of biliary lipid composition, children with bile acid malabsorption were shown to have a chenodeoxycholate-dominant pattern, an increased glycine- to taurine-conjugated bile acid ratio, and markedly supersaturated cholesterol. Such profiles may be related not only to bile acid malabsorption but also to cholestasis, presumably due to intravenous hyperalimentation.

摘要

对两名接受静脉高营养治疗的胆汁酸吸收不良患儿的胆汁酸代谢进行了检查。一名病因不明的胆汁酸吸收不良患儿的粪便胆汁酸排泄量为1261μmol/m²/天,一名因长段无神经节症手术后出现继发性胆汁酸吸收不良的患儿的粪便胆汁酸排泄量为1877μmol/m²/天。这些值比胆汁酸代谢无明显异常的腹泻或非腹泻儿童的值高约10倍。这些胆汁酸吸收不良患者的粪便胆汁酸几乎完全结合,未结合胆汁酸含量很少。肠道中胆汁酸去结合紊乱可能是由于肠道转运时间过快所致,这在我们的胆汁酸吸收不良患者中也有发现。在分析胆汁脂质成分时,胆汁酸吸收不良患儿表现出以鹅去氧胆酸盐为主的模式、甘氨酸与牛磺酸结合胆汁酸的比例增加以及胆固醇明显过饱和。这些特征可能不仅与胆汁酸吸收不良有关,还与胆汁淤积有关,推测是由于静脉高营养所致。

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