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Diabetes in patients with acromegaly treated with pegvisomant: observations from acrostudy.

Authors :
Brue T
Lindberg A
Jan van der Lely A
Akerblad AC
Koltowska-Häggström M
Gomez R
Droste M
Hey-Hadavi J
Strasburger CJ
Camacho-Hübner C
Source :
Endocrine [Endocrine] 2019 Mar; Vol. 63 (3), pp. 563-572. Date of Electronic Publication: 2018 Nov 24.
Publication Year :
2019

Abstract

Purpose: To explore the effects of pegvisomant (PEGV) on glucose metabolism in patients with acromegaly within ACROSTUDY, an international, observational, prospective safety surveillance study.<br />Methods: Patients were retrospectively divided into two cohorts, with (DM group) or without diabetes mellitus (no-DM). Parameters of glucose metabolism and IGF-I values were analyzed yearly both cross-sectionally for 4 years (yrs) and longitudinally at 1 and 4-5 yrs of PEGV treatment.<br />Results: Among 1762 patients, 510 (28.9%) had DM before PEGV start. At cross-sectional analyses, in the DM group mean blood glucose was 140.0 ± 58.7 mg/dl at baseline, 116.4 ± 44.8 mg/dl at year 1 and 120.0 ± 44.3 mg/dl at yr 4. Mean HbA1c was 6.6 ± 1.2 % at yr 1 vs. 7.0 ± 1.4 % at baseline. HbA1c was above 6.5% in 61.9% at baseline and ranged from 45.4 to 53.8% at subsequent yearly time points. At the 4-yr longitudinal analysis, in the DM group (n = 109), mean blood glucose decreased by 20.2 mg/dl at yr 4, mean HbA1c was 7.0 ± 1.5% at baseline vs. 6.8 ± 1.4%. Patients achieved IGF-I normalization in 52.1% and 57.4% of cases in the DM and no-DM groups, respectively at 1 year. The mean daily PEGV dose (mg/day) was higher in the DM group (18.2 vs. 15.3) while the absolute change of IGF-I values from baseline was similar in both groups. PEGV was well tolerated in both groups without any unexpected AEs.<br />Conclusions: Patients with DM had a moderate decrease in mean fasting glucose values during PEGV treatment.

Details

Language :
English
ISSN :
1559-0100
Volume :
63
Issue :
3
Database :
MEDLINE
Journal :
Endocrine
Publication Type :
Academic Journal
Accession number :
30474822
Full Text :
https://doi.org/10.1007/s12020-018-1792-0