Clinical Case Seminar The First Case Report of Sulfonylurea Use in a Woman with Permanent Neonatal Diabetes Mellitus due to KCNJ11 Mutation during a High-Risk Pregnancy

被引:11
作者
Klupa, Tomasz [1 ,2 ]
Kozek, Elzbieta [1 ,2 ]
Nowak, Natalia [1 ]
Cyganek, Katarzyna [1 ,2 ,6 ]
Gach, Agnieszka [3 ,4 ]
Milewicz, Tomasz [5 ]
Czajkowski, Krzysztof
Tolloczko, Justyna [7 ]
Mlynarski, Wojciech [3 ]
Malecki, Maciej T. [1 ,2 ]
机构
[1] Jagiellonian Univ, Dept Metab Dis, Coll Med, PL-31501 Krakow, Poland
[2] Univ Hosp, PL-31351 Krakow, Poland
[3] Med Univ Lodz, Dept Pediat Oncol Hematol & Diabetol, PL-90419 Lodz, Poland
[4] Polish Mothers Mem Hosp, Dept Genet, PL-93338 Lodz, Poland
[5] Jagiellonian Univ, Coll Med, Dept Gynecol Endocrinol, PL-31501 Krakow, Poland
[6] Warsaw Med Univ, Dept Obstet & Gynecol 2, PL-02091 Warsaw, Poland
[7] Warsaw Med Univ, Dept Neonatol & Neonatal Intens Care, PL-02091 Warsaw, Poland
关键词
FOLLOW-UP; ACTIVATING MUTATIONS; ORAL SULFONYLUREAS; ENCODES KIR6.2; GENE-MUTATIONS; INSULIN; GLYBURIDE; THERAPY; WOMEN; GLIBENCLAMIDE;
D O I
10.1210/jc.2010-0096
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sulfonylureas (SUs) were proven to be more effective than insulin in most Kir6.2 permanent neonatal diabetes mellitus (PNDM) patients. We report SU use during pregnancy in PNDM. A woman with the R201H Kir6.2 mutation became pregnant at the age of 37. The patient had been on glipizide 30 mg for 3 yr; her glycosylated hemoglobin level was 5.8%. She was diagnosed with chronic diabetes complications and a congenital defect of the urogenitary tract-a bicornuate uterus with septum. Because the effect of SU on fetal development is uncertain, she was switched to insulin after the pregnancy diagnosis; however, the subsequent glycemic control was unsatisfactory, with episodes of hyper- and hypoglycemia. Thus, in the second trimester, the patient was transferred to SU (glibenclamide, 40 mg), which resulted in stabilization of glycemic control; glycosylated hemoglobin in the third trimester was 5.8%. Prenatal genetic testing excluded the Kir6.2 R201H mutation in the fetus. A preterm cesarean delivery was carried out in the 35th week. The Apgar score of the newborn boy (weight, 3010 g; 75th percentile) was 8 at 1 min. He presented with hypoglycemia, transient tachypnea of the newborn, and hyperbilirubinemia. The recovery was uneventful. No birth defects were recorded. His development at the ninth month of life was normal. In summary, we show a high-risk pregnancy in long-term PNDM that despite perinatal complications ended with the birth of a healthy child. SUs, which seem to constitute an alternative to insulin during pregnancy in Kir6.2-related PNDM, were used during the conception period and most of the second and third trimesters. (J Clin Endocrinol Metab 95: 3599-3604, 2010)
引用
收藏
页码:3599 / 3604
页数:6
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