Velho G, Hattersley A T, Froguel P
INSERM Unit 342, Saint Vincent de Paul Hospital, Paris, France.
Diabetologia. 2000 Aug;43(8):1060-3. doi: 10.1007/s001250051490.
AIMS/HYPOTHESIS: Altered fetal insulin secretion caused by fetal or maternal glucokinase mutations influence birth weight. Here, we attempt to answer two additional questions: firstly, whether this variation in birth weight (from low birth weight to macrosomia) has an effect on adult height or weight. Secondly, whether maternal hyperglycaemia during fetal life has an effect on metabolic phenotypes of the adult offspring.
We studied 447 family members from 37 MODY2 kindred, divided into four groups according to the presence or absence of a glucokinase mutation in the subject (S+ or S-, respectively) and his/her mother (M+ or M-). Birth weight data were obtained from a questionnaire sent to the mothers.
Birth weight was reduced in the presence of a fetal mutation (M-S+) and increased in the presence of a maternal mutation (M+ S-). These effects are additive as similar birth weights were observed in M+ S+ and M-S- offspring. Adult height, weight or body mass index (weight/height2) were, however, similar in the four groups of subjects. Non-diabetic adult offspring, regardless of the glycaemic status of the mothers (M+ S- or M-S-), had similar insulin secretion, insulin sensitivity, blood pressures and lipid profiles. These variables as well as the severity of hyperglycaemia were similar in adult M+ S+ and M-S+ MODY2 subjects.
CONCLUSION/INTERPRETATION: Maternal environment and fetal genotypes could alter growth in utero by changing fetal insulin secretion but these effects do not result in a persistent programming in latter life.
目的/假设:胎儿或母体葡萄糖激酶突变引起的胎儿胰岛素分泌改变会影响出生体重。在此,我们试图回答另外两个问题:第一,这种出生体重的变化(从低出生体重到巨大儿)是否对成年后的身高或体重有影响。第二,胎儿期母体高血糖是否对成年后代的代谢表型有影响。
我们研究了来自37个青少年发病的成年型糖尿病2型(MODY2)家族的447名家庭成员,根据受试者(分别为S+或S-)及其母亲(分别为M+或M-)是否存在葡萄糖激酶突变分为四组。出生体重数据通过向母亲发放问卷获得。
胎儿存在突变(M-S+)时出生体重降低,母体存在突变(M+S-)时出生体重增加。这些影响是累加的,因为在M+S+和M-S-后代中观察到相似的出生体重。然而,四组受试者的成年身高、体重或体重指数(体重/身高²)相似。非糖尿病成年后代,无论母亲的血糖状态如何(M+S-或M-S-),胰岛素分泌、胰岛素敏感性、血压和血脂谱均相似。成年M+S+和M-S+的MODY2受试者的这些变量以及高血糖的严重程度相似。
结论/解读:母体环境和胎儿基因型可通过改变胎儿胰岛素分泌来改变子宫内生长,但这些影响不会导致成年后持续的编程效应。