Glycemia after Betamethasone in Pregnant Women without Diabetes-Impact of Marginal Values in the 75-g OGTT.
Ioannis KakoulidisIoannis IliasAnastasia LinardiAikaterini MichouCharalampos MilionisFoteini PetychakiEvangelia VenakiEftychia KoukkouPublished in: Healthcare (Basel, Switzerland) (2020)
Betamethasone (BM) administration in pregnancy has been shown to reduce the incidence and severity of neonatal respiratory distress syndrome. Its known diabetogenic impact, combined with placental insulin resistance, leads to a transient increase in glycemia. However, its effect on glucose homeostasis in pregnancy has not been adequately investigated. We closely monitored and assessed the glycemic profile of 83 pregnant women, with normal glucose metabolism, who were given BM during their hospitalization due to threatened premature labor. A significant change in the glycemic profile in most patients was noted, lasting 1.34 ± 1.05 days. Sixty-six of eighty-three women were eventually treated with insulin to maintain glycemia within acceptable limits. The mean ± SD insulin dosage was 12.25 ± 11.28 units/day. The need for insulin therapy was associated with higher BM doses and the presence of marginal values in the 75-g oral glucose tolerance test (OGTT) at 60 min. Our study demonstrates, following BM administration, the need for increased awareness and individualized monitoring/treatment of pregnant women with normal-yet marginal-values in the 75-g OGTT.
Keyphrases
- type diabetes
- glycemic control
- pregnant women
- pregnancy outcomes
- insulin resistance
- blood glucose
- end stage renal disease
- polycystic ovary syndrome
- newly diagnosed
- chronic kidney disease
- preterm birth
- ejection fraction
- cardiovascular disease
- prognostic factors
- risk factors
- weight loss
- high fat diet
- peritoneal dialysis
- stem cells
- adipose tissue
- case report
- skeletal muscle
- patient reported outcomes
- atomic force microscopy
- high fat diet induced
- respiratory tract
- bone marrow
- high resolution
- patient reported
- mass spectrometry
- replacement therapy
- breast cancer risk
- blood brain barrier