Candy David C A, Devane Seán P
Department of Child Health, King's College School of Medicine and Dentistry, and King's Healthcare Trust, Denmark Hill, London SE5 9RS, UK.
Semin Neonatol. 1997 Nov;2(4):255-262. doi: 10.1016/S1084-2756(97)80032-2. Epub 2006 Dec 24.
The frequency with which necrotizing enterocolitis occurs in outbreaks makes it likely that the illness can have an infective origin. Immunological and non-immunological defences of the gastrointestinal are impaired in early life. Consequently the gut of the preterm infant is predisposed to bacterial overgrowth. A wide range of pathogenic bacteria and viruses have been isolated from infants with necrotizing enterocolitis or detected histologically. The presence of bacterial metabolites in the breath, intestinal bullae (hydrogen) and urine (D-lactate) during the course of the illness is further confirmatory evidence. The presence of bacteria or bacterial products (such as exo- and endotoxin) in the circulation will lead to ischaemia of the intestine and other organs either directly or via mediators such as cytokines or platelet activating factor. Future studies in necrotizing enterocolitis should be directed to understanding and modulating inflammatory mediators in necrotizing enterocolitis and preventing the disease with breast milk and nutritional supplements (glutamine, short chain fatty acids), chemoprophylaxis, and antibodies.
坏死性小肠结肠炎在疾病暴发中的发生频率表明,这种疾病可能源于感染。胃肠道的免疫和非免疫防御在生命早期会受到损害。因此,早产儿的肠道易发生细菌过度生长。从患有坏死性小肠结肠炎的婴儿中已分离出多种致病细菌和病毒,或通过组织学检测到它们。在疾病过程中,呼出气体、肠道气泡(氢气)和尿液(D-乳酸)中存在细菌代谢产物是进一步的确证证据。循环中存在细菌或细菌产物(如外毒素和内毒素)将直接或通过细胞因子或血小板活化因子等介质导致肠道和其他器官的缺血。未来关于坏死性小肠结肠炎的研究应致力于了解和调节坏死性小肠结肠炎中的炎症介质,并通过母乳和营养补充剂(谷氨酰胺、短链脂肪酸)、化学预防和抗体来预防该疾病。