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1.
Bull Acad Natl Med ; 184(5): 995-1007; discussion 1007-8, 2000.
Article in French | MEDLINE | ID: mdl-11077720

ABSTRACT

Fetal mortality and morbidity remain dramatically increased in diabetic women. To evaluate the benefit of a preconceptional education combined with a good metabolic control, we compared the outcome of pregnancy in 2 groups of type I diabetic women: group A (n = 21) planned before conception versus group B (n = 40) not planned. Both groups were similar related to the type and duration of diabetes, its complications, age, body mass index and different factors of risk. In group A, HbA1C levels were < or = 3 SD of the normal mean of non diabetic values before conception and during the pregnancy course and > or = 3 SD in group B. We observed a significant reduction (p < 0.05) of the main adverse events regarding fetus outcome (fetal, perinatal and neonatal mortality, malformations) and obstetrical complications in the planned group. These data lead to the need of an extensive policy of early planification of pregnancy in diabetic women.


Subject(s)
Diabetes Mellitus, Type 1/therapy , Patient Education as Topic , Preconception Care/methods , Pregnancy in Diabetics/therapy , Congenital Abnormalities/prevention & control , Female , Follow-Up Studies , Humans , Hypoglycemic Agents/therapeutic use , Infant Mortality , Infant, Newborn , Insulin/therapeutic use , Pregnancy
3.
Acta Diabetol ; 33(1): 1-6, 1996 Mar.
Article in English | MEDLINE | ID: mdl-8777278

ABSTRACT

Glucose clamp experiments have shown that patients with reactive postprandial hypoglycaemia (PRH) frequently have an increased glucose disposal, but the relative involvement of insulin sensitivity (SI) and glucose effectiveness (Sg) in this process remains unknown. The minimal model approach was used to compare 13 patients in whom moderate reactive hypoglycaemia ( < 3.3 mmol) had been previously diagnosed and 13 matched controls. The intravenous glucose tolerance test (IVGTT, 0.5 g/kg glucose IV) with 0.02 U/kg insulin given at the 19th min and frequent sampling over 180 min shows that PRH patients exhibit a higher glucose tolerance coefficient Kg (2.99 +/- 0.26 vs 2.19 +/- 0.12; P < 0.02), higher SI [22.9 +/- 6.4 vs 7.18 +/- 0.14 min-1/(microU/ml). 10(-4); P < 0.01] and higher Sg (3.84 +/- 0.35 vs 2.92 +/- 0.79 min-1. 10(-2); P < 0.05). The increase in Sg is explained by an increase in its component basal insulin effectiveness (BIE: 1.2 +/- 0.27 min-1.10(-2) in PRH subjects vs 0.58 +/- 0.07; P < 0.05) rather than an increase in Sg at zero insulin. The increase in BIE results from the high values of SI. In 4 PRH subjects SI and Sg were within the normal range, and the increase in Kg evidenced in the 9 others was explained by an increase in SI alone in 3 cases, in Sg alone in 1 case, and both SI and Sg in 5 cases. Thus, in sedentary subjects, the previously reported rise in tissue glucose assimilation is mainly explained by an increased insulin-mediated glucose disposal rather than non-insulin-mediated glucose disposal.


Subject(s)
Blood Glucose/metabolism , Eating , Hypoglycemia/physiopathology , Insulin/pharmacology , Adult , Blood Glucose/drug effects , Female , Glucose/metabolism , Glucose Clamp Technique , Glucose Tolerance Test , Humans , Hypoglycemia/blood , Male , Reference Values
4.
Horm Res ; 42(1-2): 55-61, 1994.
Article in English | MEDLINE | ID: mdl-7959635

ABSTRACT

Xenopus laevis oocytes possess insulin and/or insulin-like growth factor-1 (IGF-1) receptors and respond to respective hormones by increasing glucose transport and progressing from the G2 to M phase of the cell cycle (maturation). While molecular transduction mechanisms involving mitogen-activating kinases and cyclin-dependent kinases begin to be elucidated, missing links remain between the initial receptor tyrosine phosphorylation events and downstream signaling. The discovery that phosphotyrosines produced by receptor autophosphorylation or during substrate phosphorylation serve as an anchor for src homology 2 domains of several signaling proteins had a major impact on understanding how cytoplasmic enzymes are recruited at the level of the plasma membrane for subsequent activation.


Subject(s)
Insulin-Like Growth Factor I/physiology , Insulin/physiology , Oocytes/physiology , Signal Transduction , Animals , Cellular Senescence , Genes, ras , Humans , Phosphorylation , Serine/metabolism , Threonine/metabolism , Tyrosine/metabolism
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