Pegvisomant Improves Glucose Metabolism in Acromegaly: A Meta-Analysis of Prospective Interventional Studies.
Acromegaly
/ drug therapy
Blood Glucose
/ metabolism
Body Mass Index
Cholesterol
/ metabolism
Cholesterol, HDL
/ metabolism
Cholesterol, LDL
/ metabolism
Drug Therapy, Combination
Glucose Tolerance Test
Glycated Hemoglobin
/ metabolism
Human Growth Hormone
/ analogs & derivatives
Humans
Insulin Resistance
Octreotide
/ therapeutic use
Peptides, Cyclic
/ therapeutic use
Receptors, Somatotropin
/ antagonists & inhibitors
Somatostatin
/ analogs & derivatives
Triglycerides
/ metabolism
Journal
The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362
Informations de publication
Date de publication:
01 07 2019
01 07 2019
Historique:
received:
23
10
2018
accepted:
06
03
2019
pubmed:
15
3
2019
medline:
2
6
2020
entrez:
15
3
2019
Statut:
ppublish
Résumé
Pegvisomant (PEG) in monotherapy or combined with somatostatin analogs (SSAs) is used to control acromegaly, improving metabolism. However, the metabolic changes induced by PEG have not been systematically reviewed. To address the following questions: does PEG or the combination of PEG and SSAs affect fasting plasma glucose (FPG), glycosylated Hb (HbA1c), glucose load (2-hour oral glucose tolerance test), insulin levels [fasting plasma insulin (FPI)], homeostatic model assessment of insulin resistance (HOMA-I), homeostatic model assessment of β-cell function, lipid profile, or body mass index? Are the effects disease-related or drug-related? Indexed databases up to January 2019. Prospective interventional trials reporting glycometabolic outcomes under PEG or PEG plus SSAs for a minimum of 6 months. Three reviewers screened eligible publications (7248), three others extracted the outcomes, and all assessed the risk of biases. Thirteen studies were included in the PEG and 5 in the PEG plus SSAs analysis (overall 550 subjects). PEG significantly decreased FPG [effect size (ES) -0.80 mmol/L (95% CI, -1.06 to -0.55); P = 0.000], HbA1c [ES -0.43% (95% CI, -0.56 to -0.31); P = 0.000], FPI [ES -5.31 mU/L (95% CI, -10.23 to -0.39); P = 0.034], and HOMA-I [ES -0.61 (95% CI, -1.17 to -0.04); P = 0.034]. Effects on FPG and FPI were not correlated to IGF-1 changes. The addition of PEG to SSAs mitigated the effects of SSAs on metabolism, producing an overall neutral effect. Independently of disease control, PEG in monotherapy or combined with SSAs seems to improve glucose metabolism, reducing FPG, HbA1c, FPI, and HOMA-I.
Identifiants
pubmed: 30869797
pii: 5376631
doi: 10.1210/jc.2018-02281
doi:
Substances chimiques
Blood Glucose
0
Cholesterol, HDL
0
Cholesterol, LDL
0
Glycated Hemoglobin A
0
Peptides, Cyclic
0
Receptors, Somatotropin
0
Triglycerides
0
hemoglobin A1c protein, human
0
lanreotide
0G3DE8943Y
Human Growth Hormone
12629-01-5
Somatostatin
51110-01-1
Cholesterol
97C5T2UQ7J
pegvisomant
N824AOU5XV
Octreotide
RWM8CCW8GP
Types de publication
Journal Article
Meta-Analysis
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2892-2902Informations de copyright
Copyright © 2019 Endocrine Society.