Discordant biochemical parameters of acromegaly remission do not influence the prevalence or aggressiveness of metabolic comorbidities: a single-center study.
Acromegaly
GH
IGF-1
complications
discrepancy
metabolic
Journal
Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782
Informations de publication
Date de publication:
2023
2023
Historique:
received:
11
07
2023
accepted:
06
09
2023
medline:
2
11
2023
pubmed:
13
10
2023
entrez:
13
10
2023
Statut:
epublish
Résumé
The discrepancy between the biomarkers of disease's activity in acromegalic patients (GH and IGF-1) is almost frequent representing a challenge for the development of comorbidities in the long term. The aim of this study was to evaluate the prevalence and severity of metabolic comorbidities (diabetes, hypertension, and dyslipidemia) in surgically treated acromegalic patients with disease control and discordant GH and/or IGF-1 levels compared with those with concordant values. Retrospective monocentric observational study on acromegalic surgically treated patients with biochemical remission (group A) or mild discordant GH or IGF-1 levels (group B). Metabolic complications and medical therapy were assessed at diagnosis and at the last follow-up visit. Severity of the disease was set for drug titration or shift to another molecule or more than before. There were 18 patients that met the inclusion criteria [group A: nine patients; group B: nine patients, follow-up 7 years (IQR 5.0;11.25)]. The prevalence of female patients was significantly higher in the remission group compared with the discordant group (p < 0.02). Considering metabolic complications, at the last follow-up, 61.1% was affected by hypertension, 33.3% by diabetes, and 61.1% by dyslipidemia, without differences between groups. Drug characteristics (dose, shift, number) during the follow-up did not differ significantly between groups. Metabolic complications, mainly dyslipidemia, are frequent in cured acromegalic patients, but GH/IGF-1 discrepancy does not seem to represent a risk factor for their presence or persistence. More extended studies are needed to confirm our results in a long-term period.
Identifiants
pubmed: 37829686
doi: 10.3389/fendo.2023.1256975
pmc: PMC10565344
doi:
Substances chimiques
Human Growth Hormone
12629-01-5
Insulin-Like Growth Factor I
67763-96-6
Types de publication
Observational Study
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1256975Informations de copyright
Copyright © 2023 Romanisio, Pitino, Ferrero, Pizzolitto, Costelli, Antoniotti, Marzullo, Aimaretti, Prodam and Caputo.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
Références
Nat Rev Endocrinol. 2018 Sep;14(9):552-561
pubmed: 30050156
J Endocrinol Invest. 2020 Apr;43(4):529-538
pubmed: 31741320
Endocr Rev. 2004 Feb;25(1):102-52
pubmed: 14769829
J Clin Invest. 2009 Nov;119(11):3189-202
pubmed: 19884662
J Clin Endocrinol Metab. 2021 May 13;106(6):1783-1792
pubmed: 33544833
J Endocrinol Invest. 2022 Oct;45(10):1955-1965
pubmed: 35748978
Pituitary. 2012 Dec;15(4):562-70
pubmed: 22183781
Hypertension. 2018 Jun;71(6):e13-e115
pubmed: 29133356
Trends Endocrinol Metab. 2016 Jul;27(7):470-483
pubmed: 27229934
Endocr Rev. 2019 Feb 1;40(1):268-332
pubmed: 30184064
J Clin Endocrinol Metab. 2010 Aug;95(8):3648-56
pubmed: 20463098
Endocrine. 2020 Oct;70(1):134-142
pubmed: 32562181
Eur J Endocrinol. 2018 Jul;179(1):59-71
pubmed: 29764907
Endocrinol Metab Clin North Am. 2019 Dec;48(4):779-793
pubmed: 31655776
J Clin Endocrinol Metab. 2014 Nov;99(11):3933-51
pubmed: 25356808
J Clin Endocrinol Metab. 2014 Nov;99(11):4124-32
pubmed: 25137427
Nat Rev Dis Primers. 2019 Mar 21;5(1):20
pubmed: 30899019
Cells. 2021 Jun 02;10(6):
pubmed: 34199514
Endocrine. 2020 Apr;68(1):16-31
pubmed: 32060689
Eur J Endocrinol. 2011 Jun;164(6):885-9
pubmed: 21471168
Eur J Endocrinol. 2017 May;176(5):645-655
pubmed: 28246150
J Clin Endocrinol Metab. 2008 Apr;93(4):1324-30
pubmed: 18230660
J Clin Endocrinol Metab. 2021 Mar 8;106(3):789-801
pubmed: 33236108
J Endocrinol Invest. 2019 Apr;42(4):397-402
pubmed: 30069856
Pituitary. 2020 Oct;23(5):582-594
pubmed: 32602066
Eur J Endocrinol. 2018 Jan;178(1):65-74
pubmed: 28993415
Clin Endocrinol (Oxf). 2016 Nov;85(5):681-688
pubmed: 27292418
Neuroendocrinology. 2022;112(1):1-14
pubmed: 33454712
Endocr Rev. 2004 Oct;25(5):693-721
pubmed: 15466938
J Clin Endocrinol Metab. 2020 Apr 1;105(4):
pubmed: 31606735
Eur Heart J. 2020 Jan 1;41(1):111-188
pubmed: 31504418