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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:修复性结肠切除术后患者的乳糖不耐症,乳糖吸收不良和成年型泌乳不足的遗传易感性

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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:这项研究提供了关于72例恢复性直肠结肠切除术(RPC)后乳糖吸收不良,乳糖不耐症和成年型泌乳不足的遗传易感性的最新发现。通过氢-甲烷呼气试验评估乳糖吸收不良。通过检测乳糖酶基因中的–13910T / C多态性,评估成年型泌乳不足的遗传易感性。 UC(溃疡性结肠炎)患者的乳糖不耐症较FAP(家族性腺瘤性息肉病)患者更为常见(77.5%vs. 55.2%; p = 0.01)。在39.1%的受试者中观察到了乳糖酶基因的C / C基因型,在UC和FAP患者之间没有显着差异。乳糖吸收不良发生在10.1%的受试者中,并且几乎仅在具有遗传易感性的患者中发生,在UC和FAP患者中发生频率相同。

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