Viswanathan Lavanya, Rao Satish S C, Kennedy Kevin, Sharma Amol, Yan Yun, Jimenez Enoe
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Augusta University, Augusta, GA, USA.
J Neurogastroenterol Motil. 2020 Jul 30;26(3):384-390. doi: 10.5056/jnm19167.
BACKGROUND/AIMS: Disaccharidase assay is used for assessing carbohydrate intolerance in children, but its usefulness in adults is not known. The aim of this study is to assess the prevalence of disaccharidase deficiency in patients with unexplained gastrointestinal symptoms.
A retrospective review of adults with chronic (> 1 year) abdominal symptoms and negative imaging and endoscopy/colonoscopy and who completed bowel symptom questionnaire and duodenal biopsy for lactase, maltase, sucrase, and palatinase was performed. A subset also underwent 25 g lactose breath test (LBT).
One hundred twenty patients (females = 83) were evaluated, of whom 48 also underwent LBT. Fifty-six (46.7%) patients had enzyme deficiency; 44 (36.7%) had single (either lactase or maltase), 1 had 3 enzyme deficiencies, 11 (9.2 %) had all 4 disaccharidase enzyme (pan-disaccharidase) deficiency, and 64 (53.0%) had normal enzyme levels. Baseline prevalence and severity of 11 gastrointestinal symptoms were similar between normal and single enzyme deficiency groups. The sensitivity and specificity of LBT was 78.3% and 72.0%, respectively and overall agreement with lactase deficiency was 75.0%.
Isolated disaccharidase deficiency occurs in adults, usually lactase and rarely maltase, and pan-disaccharidase deficiency is rare. Baseline symptoms or its severity did not predict enzyme deficiency.
背景/目的:双糖酶检测用于评估儿童的碳水化合物不耐受情况,但其在成人中的作用尚不清楚。本研究旨在评估不明原因胃肠道症状患者中双糖酶缺乏的患病率。
对患有慢性(>1年)腹部症状、影像学及内镜/结肠镜检查阴性的成人进行回顾性研究,这些患者完成了肠道症状问卷以及乳糖酶、麦芽糖酶、蔗糖酶和帕拉金酶的十二指肠活检。一部分患者还接受了25g乳糖呼气试验(LBT)。
共评估了120例患者(女性83例),其中48例还接受了LBT。56例(46.7%)患者存在酶缺乏;44例(36.7%)为单一酶缺乏(乳糖酶或麦芽糖酶),1例有3种酶缺乏,11例(9.2%)存在所有4种双糖酶(全双糖酶)缺乏,64例(53.0%)酶水平正常。正常组和单一酶缺乏组11种胃肠道症状的基线患病率和严重程度相似。LBT的敏感性和特异性分别为78.3%和72.0%,与乳糖酶缺乏的总体一致性为75.0%。
成人中存在孤立性双糖酶缺乏,通常为乳糖酶缺乏,麦芽糖酶缺乏罕见,全双糖酶缺乏则更为罕见。基线症状及其严重程度无法预测酶缺乏情况。