Francis-Emmanuel Patrice M, Thompson Debbie S, Barnett Alan T, Osmond Clive, Byrne Christopher D, Hanson Mark A, Gluckman Peter D, Forrester Terrence E, Boyne Michael S
Tropical Medicine Research Institute (P.M.F.-E., D.S.T., A.T.B., T.E.F., M.S.B.) and Department of Surgery, Radiology, Anaesthesia, and Intensive Care (A.T.B.), The University of the West Indies, Mona, Kingston 7, Jamaica, West Indies; Medical Research Council Lifecourse Epidemiology Unit (C.O.), Institute of Developmental Sciences (M.A.H.) and Nutrition and Metabolism Unit (C.D.B.), School of Medicine, University of Southampton, Southampton SO16 6YD, United Kingdom; and Centre for Human Evolution, Adaptation, and Disease (P.D.G.), Liggins Institute, University of Auckland, Auckland 1142, New Zealand.
J Clin Endocrinol Metab. 2014 Jun;99(6):2233-40. doi: 10.1210/jc.2013-3511. Epub 2014 Feb 11.
The clinical syndromes of severe acute malnutrition may have early life origins because children with marasmus have lower birth weight than those with kwashiorkor. We hypothesized that resultant metabolic effects may persist into adulthood. We investigated whether marasmus survivors (MS) are more insulin resistant and glucose intolerant than kwashiorkor survivors (KS).
This was a case-control study in Jamaican adults.
We performed oral glucose tolerance tests on 191 adults (aged 17-50 y; 52% male; body mass index 24.2 ± 5.5 kg/m(2)). There were 43 MS; 38 KS; 70 age-, sex-, and body mass index-matched community controls; and 40 age- and birth weight-matched controls.
We measured insulin sensitivity with the whole-body insulin sensitivity index, and β-cell function with the insulinogenic index and the oral disposition index.
Fasting glucose was comparable across groups, but glucose intolerance was significantly more common in MS (19%) than in KS (3%), community controls (11%), and birth weight-matched controls (10%). The whole-body insulin sensitivity index was lower in MS than KS (P = .06) but similar between MS and controls. The insulinogenic index and oral disposition index were lower in MS compared with all three groups (P < .01).
Marasmus survivors tend to be less insulin sensitive, but have significantly lower insulin secretion and are more glucose intolerant compared with kwashiorkor survivors and controls. This suggests that poor nutrition in early life causes β-cell dysfunction, which may predispose to the development of diabetes.
严重急性营养不良的临床综合征可能源于生命早期,因为消瘦型营养不良患儿的出生体重低于夸希奥科病患儿。我们推测由此产生的代谢影响可能会持续到成年期。我们调查了消瘦型营养不良幸存者(MS)是否比夸希奥科病幸存者(KS)更具胰岛素抵抗和葡萄糖不耐受性。
这是一项针对牙买加成年人的病例对照研究。
我们对191名成年人(年龄17 - 50岁;52%为男性;体重指数24.2±5.5kg/m²)进行了口服葡萄糖耐量试验。其中有43名MS;38名KS;70名年龄、性别和体重指数匹配的社区对照者;以及40名年龄和出生体重匹配的对照者。
我们用全身胰岛素敏感性指数测量胰岛素敏感性,用胰岛素生成指数和口服处置指数测量β细胞功能。
各组间空腹血糖相当,但葡萄糖不耐受在MS中(19%)比在KS中(3%)、社区对照者中(11%)和出生体重匹配的对照者中(10%)明显更常见。MS的全身胰岛素敏感性指数低于KS(P = 0.06),但与对照者相似。与所有三组相比,MS的胰岛素生成指数和口服处置指数较低(P < 0.01)。
与夸希奥科病幸存者及对照者相比,消瘦型营养不良幸存者往往胰岛素敏感性较低,但胰岛素分泌显著减少且葡萄糖不耐受性更高。这表明生命早期的营养不良会导致β细胞功能障碍,这可能易引发糖尿病。