首页> 外文期刊>Acta Biochimica Polonica >Lactose intolerance, lactose malabsorption and genetic predisposition to adult-type hypolactasia in patients after restorative proctocolectomy
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Lactose intolerance, lactose malabsorption and genetic predisposition to adult-type hypolactasia in patients after restorative proctocolectomy

机译:乳糖不耐受,乳糖不耐受性和遗传性易受术治疗后患者成人型低解瘤切除术治疗

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摘要

This study provides up-to-date findings on lactose malabsorption, lactose intolerance and genetic predisposition to adult-type hypolactasia in 72 patients after restorative proctocolectomy (RPC). The lactose malabsorption was assessed by hydrogen-methane breath test. Genetic predisposition to adult-type hypolactasia was assessed by detecting -13910T/C polymorphism in the lactase gene. Lactose intolerance was more frequent in UC (ulcerative colitis) patients than FAP (familial adenomatous polyposis) patients (77.5% vs. 55.2%; p=0.01). The C/C genotype of the lactase gene was observed in 39.1% subjects with no significant difference between UC and FAP patients. Lactose malabsorption occurred in 10.1% of subjects and almost only in patients with genetic predisposition, with the same frequency in UC and FAP patients.
机译:本研究提供了在恢复性ProctocolcoMy(RPC)后72名患者成人型低辐射症对成人型低解障的最新结果。 通过氢甲烷呼吸试验评估乳糖吸收理。 通过检测乳糖酶基因中的-13910t / c多态性来评估成人型低actacisia的遗传倾向。 在UC(溃疡性结肠炎)患者比FAP(家族性腺瘤性息肉)患者(77.5%vs.5.2%; P = 0.01),在UC(溃疡性结肠炎)患者中更频繁。 在39.1%受试者中观察到乳糖酶基因的C / C基因型,UC和FAP患者无显着差异。 乳糖吸收吸收在10.1%的受试者中发生,几乎只在遗传易感性患者中,在UC和FAP患者中具有相同的频率。

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