Martikainen A, Saukkonen T, Kulmala P K, Reijonen H, Ilonen J, Teramo K, Koskela P, Knip M, Akerblom H K
Department of Pediatrics, University of Oulu, Finland.
Diabetes. 1996 Dec;45(12):1706-10. doi: 10.2337/diab.45.12.1706.
We studied 20 infants of mothers with IDDM participating in a pilot study for a dietary intervention trial, testing the hypothesis that avoidance of cow's milk proteins early in life will reduce the risk of subsequent IDDM. The aim was to evaluate the elimination of IDDM-associated antibodies from the peripheral circulation of the infants, the possible emergence of autoantibodies indicating beta-cell destruction, and the influence of the dietary intervention and genetic disease susceptibility on the development of these autoantibodies. Transplacentally transferred islet cell antibodies (ICAs) and antibodies to the 65-kDa isoform of glutamic acid decarboxylase (GAD65As) disappeared from the peripheral circulation of most infants over the first few months of life and in all infants before the age of 9 months. Insulin antibodies were eliminated before the same age in all cases but one. The higher the initial antibody level was, the longer the time required for elimination. Four infants tested positive for insulin autoantibodies (IAAs) on at least one occasion during the first year of life, and 5 out of 16 unaffected subjects (31%) had IAAs at the age of 2 years. One infant became positive for IAA before the age of 6 months, with increasing levels later, seroconverted to positivity for ICAs and GAD65As between 6 and 9 months and presented with clinical IDDM at the age of 14 months. He had the HLA DQB1*0302/x genotype, which predisposes carriers to IDDM, and had been given the casein hydrolysate formula as supplementary milk. There were no significant differences in the levels of various autoantibodies between two groups of subjects defined either on the type of dietary intervention or the degree of genetic susceptibility. The findings indicate that transplacentally transferred antibodies related to IDDM are usually eliminated from the peripheral circulation of infants before 9 months of age and that IDDM-associated autoantibodies may emerge before the age of 6 months. Our results also illustrate that avoidance of cow's milk proteins over the first 9 months of life does not provide total protection against IDDM.
我们研究了20名患有胰岛素依赖型糖尿病(IDDM)母亲的婴儿,这些婴儿参与了一项饮食干预试验的初步研究,该试验检验了这样一个假设:生命早期避免摄入牛奶蛋白将降低后续患IDDM的风险。目的是评估婴儿外周循环中与IDDM相关抗体的清除情况、表明β细胞破坏的自身抗体的可能出现情况,以及饮食干预和遗传疾病易感性对这些自身抗体产生的影响。经胎盘转移的胰岛细胞抗体(ICAs)和针对谷氨酸脱羧酶65-kDa同工型的抗体(GAD65As)在大多数婴儿出生后的头几个月从外周循环中消失,在所有婴儿9个月龄之前全部消失。除一例之外,所有病例中的胰岛素抗体在相同年龄之前被清除。初始抗体水平越高,清除所需时间越长。4名婴儿在出生后第一年至少有一次检测胰岛素自身抗体(IAAs)呈阳性,16名未受影响的受试者中有5名(31%)在2岁时检测出IAAs。一名婴儿在6个月龄之前IAA呈阳性,随后水平升高,在6至9个月之间血清转化为ICA和GAD65A阳性,并在14个月龄时出现临床IDDM。他具有HLA DQB1*0302/x基因型,该基因型使携带者易患IDDM,并且他曾被给予酪蛋白水解物配方作为补充奶。根据饮食干预类型或遗传易感性程度定义的两组受试者之间,各种自身抗体水平没有显著差异。研究结果表明,与IDDM相关的经胎盘转移抗体通常在婴儿9个月龄之前从外周循环中清除,并且与IDDM相关的自身抗体可能在6个月龄之前出现。我们的结果还表明,在生命的前9个月避免摄入牛奶蛋白并不能完全预防IDDM。