Impaired Insulin Secretion After Prenatal Exposure to the Dutch Famine

OBJECTIVE:--We previously reported that people prenatally exposed to famine during the Dutch Hunger Winter of 1944-1945 have higher 2-h glucose concentrations after an oral glucose tolerance test in later life. We aimed to determine whether this association is mediated through alterations in insulin...

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Veröffentlicht in:Diabetes care 2006-08, Vol.29 (8), p.1897-1901
Hauptverfasser: Rooij, Susanne R. de, Painter, Rebecca C, Phillips, David I.W, Osmond, Clive, Michels, Robert P.J, Godsland, Ian F, Bossuyt, Patrick M.M, Bleker, Otto P, Roseboom, Tessa J
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Zusammenfassung:OBJECTIVE:--We previously reported that people prenatally exposed to famine during the Dutch Hunger Winter of 1944-1945 have higher 2-h glucose concentrations after an oral glucose tolerance test in later life. We aimed to determine whether this association is mediated through alterations in insulin secretion, insulin sensitivity, or a combination of both. RESEARCH DESIGN AND METHODS--We performed a 15-sample intravenous glucose tolerance test in a subsample of 94 normoglycemic men and women from the Dutch Famine Birth Cohort. We used the disposition index, derived as the product of insulin sensitivity and the first-phase insulin response to glucose as a measure of the activity of the β-cells adjusted for insulin resistance. In all analyses, we adjusted for sex and BMI. RESULTS:--Glucose tolerance was impaired in people who had been prenatally exposed to famine compared with people unexposed to famine (difference in intravenous glucose tolerance test Kg value -21% [95% CI -41 to -4]). People exposed to famine during midgestation had a significantly lower disposition index (-53% [-126 to -3]) compared with people unexposed to famine. Prenatal exposure to famine during early gestation was also associated with a lower disposition index, but this difference did not reach statistical significance. CONCLUSIONS:--Impaired glucose tolerance after exposure to famine during mid-gestation and early gestation seems to be mediated through an insulin secretion defect.
ISSN:0149-5992
1935-5548
DOI:10.2337/dc06-0460