Inverse association between 1,5-anhydroglucitol and neonatal diabetic complications.


Journal

Endocrine
ISSN: 1559-0100
Titre abrégé: Endocrine
Pays: United States
ID NLM: 9434444

Informations de publication

Date de publication:
11 2019
Historique:
received: 27 12 2018
accepted: 08 08 2019
pubmed: 23 8 2019
medline: 28 5 2020
entrez: 23 8 2019
Statut: ppublish

Résumé

A glycemic control marker to predict neonatal diabetic complications is unavailable. We aimed to examine if 1,5-anhydroglucitol (1,5-AG) can predict neonatal complications in women with diabetes in pregnancy. Prospective observational study from December 2011 to August 2013. We recruited 105 women, 70 diabetic (gestational and pregestational) and 35 nondiabetic. 1,5-AG at birth was compared between the two groups. In the diabetic group 1,5-AG, HbA1c, and fructosamine were measured before glycemic control initiation (first visit), after 4-6 weeks (second visit), and at delivery. Women were divided to poor (1,5-AG values below median at birth) and good (1,5-AG values at median and above) glycemic control groups. Mean daily glucose charts were collected. The primary outcome was a composite of neonatal diabetic complications: respiratory distress, hypoglycemia, polycythemia, hyperbilirubinemia, and large for gestational age. Mean 1,5-AG in the nondiabetic group was similar to that of the diabetic group without the composite outcome and was significantly higher than in the diabetic group with the composite outcome. The rate of the composite outcome was higher in the poor glycemic control group compared with the good glycemic control group (adjusted odds ratio (OR) 3.8 95% CI [1.2-12.3]). Only 1,5-AG was inversely associated with the composite outcome at all time points; the second visit was the only independent risk factor in multivariable logistic regression (OR 0.7 95% CI 0.54-0.91). The rest of the glycemic markers were not associated with neonatal composite outcome. 1,5-AG is inversely associated with neonatal diabetic complications and is superior to other glycemic markers in predicting those complications.

Identifiants

pubmed: 31435861
doi: 10.1007/s12020-019-02058-w
pii: 10.1007/s12020-019-02058-w
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
Fructosamine 4429-04-3
1,5-anhydroglucitol 54BB3B7XMZ
Deoxyglucose 9G2MP84A8W

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

210-219

Références

Am J Physiol. 1990 Mar;258(3 Pt 1):E423-7
pubmed: 2138419
Clin Chem. 1983 Jul;29(7):1396-8
pubmed: 6345028
Am J Obstet Gynecol. 1982 Dec 1;144(7):768-73
pubmed: 7148898
Endocr Pract. 2015 Jul;21(7):725-33
pubmed: 25786553
Endocr Pract. 2003 Mar-Apr;9(2):137-9
pubmed: 12917076
Acta Obstet Gynecol Scand. 1990;69(6):479-85
pubmed: 2284896
World J Diabetes. 2015 Jul 25;6(8):1045-56
pubmed: 26240701
Diabetologia. 2013 Apr;56(4):709-13
pubmed: 23377619
Diabetes Res Clin Pract. 1994 Oct;24 Suppl:S261-8
pubmed: 7859616
Obstet Gynecol. 2018 Feb;131(2):406-408
pubmed: 29370044
Diabetes Care. 2017 Sep;40(9):1181-1186
pubmed: 28724718
Am J Obstet Gynecol. 1989 Sep;161(3):593-9
pubmed: 2675597
Isr Med Assoc J. 2005 May;7(5):311-4
pubmed: 15909464
Am J Obstet Gynecol. 2004 Aug;191(2):576-81
pubmed: 15343240
Eur J Obstet Gynecol Reprod Biol. 2015 Jun;189:55-8
pubmed: 25864111
Expert Rev Mol Diagn. 2008 Jan;8(1):9-19
pubmed: 18088226
Am J Obstet Gynecol. 1987 Sep;157(3):758-63
pubmed: 3631178
Am J Obstet Gynecol. 2016 Sep;215(3):287-97
pubmed: 27133007
Diabetes Technol Ther. 2003;5(3):355-63
pubmed: 12828817
Diabetes. 1979 Dec;28(12):1039-57
pubmed: 510803
J Biochem. 1981 Jul;90(1):157-62
pubmed: 7287673
N Engl J Med. 1995 Nov 9;333(19):1237-41
pubmed: 7565999
Am J Obstet Gynecol. 1994 Apr;170(4):1036-46; discussion 1046-7
pubmed: 8166187
Diabetes Care. 2019 Jan;42(Suppl 1):S13-S28
pubmed: 30559228
Diabetes Care. 2008 Aug;31(8):1534-5
pubmed: 18426859
Diabetes Care. 2006 Jun;29(6):1214-9
pubmed: 16731998
Obstet Gynecol. 2003 Oct;102(4):850-6
pubmed: 14551018
Am J Perinatol. 2016 Jan;33(2):151-6
pubmed: 26332585
Am J Physiol. 1992 Aug;263(2 Pt 1):E268-73
pubmed: 1514606

Auteurs

Enav Yefet (E)

Department of Obstetrics & Gynecology, Emek Medical Center, Afula, Israel. enavy1@gmail.com.

Shams Twafra (S)

Department of Human Biology, Faculty of Natural Sciences, University of Haifa, Mount Carmel, Haifa, Israel.
Clinical Chemistry Laboratory, Emek Medical Center, Afula, Israel.

Neta Shwartz (N)

Clinical Chemistry Laboratory, Emek Medical Center, Afula, Israel.

Noura Hissin (N)

Department of Obstetrics & Gynecology, Emek Medical Center, Afula, Israel.

Jamal Hasanein (J)

Neonatology Department, Emek Medical Center, Afula, Israel.

Raul Colodner (R)

Rappaport Faculty of Medicine, Technion, Haifa, Israel.
Molecular Microbiology Laboratory, Emek Medical Center, Afula, Israel.

Neetsa Mirsky (N)

Department of Human Biology, Faculty of Natural Sciences, University of Haifa, Mount Carmel, Haifa, Israel.

Zohar Nachum (Z)

Department of Obstetrics & Gynecology, Emek Medical Center, Afula, Israel.
Rappaport Faculty of Medicine, Technion, Haifa, Israel.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH