Betatrophin is downregulated in pregnant women with a history of RYGB operation and a high risk of postprandial hypoglycaemia.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
04 08 2020
Historique:
received: 28 02 2020
accepted: 22 06 2020
entrez: 6 8 2020
pubmed: 6 8 2020
medline: 15 12 2020
Statut: epublish

Résumé

Betatrophin is a liver and adipose tissue-derived protein which has recently been linked to glucose metabolism. So far, no data exist about the role of betatrophin in pregnant women with a history of Roux-En-Y gastric bypass (RYGB) operation with a high risk of postprandial hypoglycaemia. In this prospective clinical study, an oral glucose tolerance test (OGTT) and an intravenous glucose tolerance test (IVGTT) were performed between the 24th and 28th week of pregnancy and 3-6 months post-partum in a cohort of obese and normal-weight pregnant women, as well as in women with a history of RYGB operation. In the cohort of pregnant women with RYGB and exaggerated risk of postprandial hypoglycaemic events, basal and dynamic betatrophin levels during the OGTT were lower than in the obese or normal-weight pregnant women (basal levels: 13.66 ± 5.88 vs. 19.03 ± 4.15 vs. 15.68 ± 6.48, p = 0.016; OGTT 60': 13.33 ± 5.40 vs. 17.37 ± 3.16 vs. 15.84 ± 4.99, p = 0.030). During the OGTT, basal and dynamic betatrophin levels at 60' were positively associated with glucose levels at 60 min (r = 0.55, p = 0.01 and r = 0.45, p = 0.039). This positive association was followed by significant hypoglycaemic events in the RYGB group. It was only in the RYGB group that betatrophin was negatively related to the disposition index (rho = -0.53, p = 0.014). After pregnancy there was a decrease in basal and stimulated betatrophin levels during the OGTT in all three patient groups. In comparison to normal-weight and obese pregnant women, women with a history of RYGB operation and a high risk of postprandial hypoglycaemic events have lower levels of betatrophin. This indicate a mechanistic role in order to decrease the risk of postprandial hypoglycaemia in this specific cohort.

Identifiants

pubmed: 32753693
doi: 10.1038/s41598-020-70075-1
pii: 10.1038/s41598-020-70075-1
pmc: PMC7403341
doi:

Substances chimiques

ANGPTL8 protein, human 0
Angiopoietin-Like Protein 8 0
Angiopoietin-like Proteins 0
Peptide Hormones 0

Types de publication

Clinical Trial Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

13152

Références

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Auteurs

Michael Leutner (M)

Unit of Gender Medicine, Clinical Division of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Caspar Matzhold (C)

Section for Science of Complex Systems, CeMSIIS, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria.
Complexity Science Hub Vienna, Josefstädter Strasse 39, 1080, Vienna, Austria.

Luise Bellach (L)

Unit of Gender Medicine, Clinical Division of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Carola Deischinger (C)

Unit of Gender Medicine, Clinical Division of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.

Stefan Thurner (S)

Section for Science of Complex Systems, CeMSIIS, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria.
Complexity Science Hub Vienna, Josefstädter Strasse 39, 1080, Vienna, Austria.
Santa Fe Institute, 1399 Hyde Park Road, Santa Fe, NM, 85701, USA.
IIASA, Schlossplatz 1, 2361, Laxenburg, Austria.

Peter Klimek (P)

Section for Science of Complex Systems, CeMSIIS, Medical University of Vienna, Spitalgasse 23, 1090, Vienna, Austria.
Complexity Science Hub Vienna, Josefstädter Strasse 39, 1080, Vienna, Austria.

Alexandra Kautzky-Willer (A)

Unit of Gender Medicine, Clinical Division of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria. alexandra.kautzky-willer@meduniwien.ac.at.
Gender Institute, 3571, Gars am Kamp, Austria. alexandra.kautzky-willer@meduniwien.ac.at.

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