Cohen Stanley A, Oloyede Hannah, Gold Benjamin D, Mohammed Aminu, Elser Heather E
Children's Center for Digestive Health Care, LLC.
Children's Healthcare of Atlanta, Atlanta, GA.
J Pediatr Gastroenterol Nutr. 2018 Jun;66 Suppl 3:S56-S60. doi: 10.1097/MPG.0000000000001961.
The epidemiology and clinical significance of disaccharidase deficiencies have not been thoroughly characterized. Recent work suggests at least genetic sucrase-isomaltase deficiency is more prevalent than previously believed. Because lactase deficiency (LD) is well described, the present study focuses on the clinical characteristics of children with disaccharidase deficiencies determined by esophagogastroduodenoscopy.
Endoscopic records were reviewed from patients undergoing esophagogastroduodenoscopies with biopsies assayed for disaccharidase activity performed by 13 pediatric gastroenterologists during 5 years (2010-2014). Presenting symptoms, clinical and histological diagnosis, treatment, disaccharidase results, and demographic variables were obtained from medical and endoscopic records of those with maltase and sucrase deficiency (SD).
Among 963 patients undergoing intestinal disaccharidase testing, 73 (7.6%) had SD on biopsy (enzyme activity <25 μmol · min · g). Thirty-four (34/73; 47%) had normal duodenal histology and are the focus of this report. Four patients had SD without LD. Pan-disaccharidase deficiency was observed in 24 patients when maltase and palatinase assays were obtained (n = 646), and 11 had SD + LD when just those 2 enzymes were analyzed (n = 317). Those with SD without LD were younger 4.6 ± 6.1 versus 14.1 ± 3.6 years and uniformly presented with diarrhea. Patients with pan-disaccharidase deficiency or SD + LD primarily reported abdominal pain (33/35; 94%), diarrhea (16/35; 46%), nausea (14/35; 40%); and poor weight gain/weight loss (10/35; 29%); constipation, flatulence, and bloating were also noted. Maltase deficiency is less common (8/963; 0.8%), presenting with similar symptoms.
Genetic sucrase-isomaltase deficiency often occurs together with lactase or pan-disaccharide deficiency. Disaccharidase deficiency should be considered a potential cause of abdominal pain and/or diarrhea in children and adolescents.
双糖酶缺乏症的流行病学及临床意义尚未得到充分阐明。近期研究表明,至少遗传性蔗糖酶 - 异麦芽糖酶缺乏症比之前认为的更为普遍。由于乳糖酶缺乏症(LD)已有详尽描述,本研究聚焦于通过食管胃十二指肠镜检查确定的双糖酶缺乏症患儿的临床特征。
回顾了13位儿科胃肠病学家在5年(2010 - 2014年)期间对接受食管胃十二指肠镜检查并进行活检以检测双糖酶活性的患者的内镜记录。从患有麦芽糖酶和蔗糖酶缺乏症(SD)患者的医疗及内镜记录中获取其症状表现、临床及组织学诊断、治疗情况、双糖酶检测结果以及人口统计学变量。
在963例接受肠道双糖酶检测的患者中,73例(7.6%)活检显示有SD(酶活性<25 μmol·min·g)。34例(34/73;47%)十二指肠组织学正常,为本报告的重点研究对象。4例患者仅有SD而无LD。在进行麦芽糖酶和帕拉金酶检测时(n = 646),24例患者存在全双糖酶缺乏;仅分析这两种酶时(n = 317),11例患者有SD + LD。无LD的SD患者年龄更小,分别为4.6 ± 6.1岁和14.1 ± 3.6岁,且均表现为腹泻。全双糖酶缺乏或SD + LD的患者主要报告有腹痛(33/35;94%)、腹泻(16/35;46%)、恶心(14/35;40%)以及体重增加缓慢/体重减轻(10/35;29%);还提到有便秘、肠胃胀气和腹胀。麦芽糖酶缺乏症较少见(8/963;0.8%),症状相似。
遗传性蔗糖酶 - 异麦芽糖酶缺乏症常与乳糖酶或全双糖酶缺乏共同出现。双糖酶缺乏症应被视为儿童和青少年腹痛和/或腹泻的潜在病因。