Metabolic Fingerprint of Acromegaly and Its Potential Usefulness in Clinical Practice
Biagetti, Betina 
(Hospital Universitari Vall d'Hebron)
Herance, José Raul 
(Vall d'Hebron Institut de Recerca (VHIR))
Ferrer Costa, Roser 
(Vall d'Hebron Institut de Recerca (VHIR))
Aulinas, Anna 
(Hospital Universitari de Vic)
Palomino-Schätzlein, Martina (Centro de Investigación Príncipe Felipe (València))
Mesa Manteca, Jordi 
(Vall d'Hebron Institut de Recerca (VHIR))
Castaño, Justo P.
(Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y Nutrición)
Luque, Raul M. (Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y Nutrición)
Simó Canonge, Rafael
(Vall d'Hebron Institut de Recerca (VHIR))
Universitat Autònoma de Barcelona
| Data: |
2019 |
| Resum: |
Insulin-like growth factor-1 (IGF-1) and growth hormone (GH) levels are the main targets for monitoring acromegaly activity, but they are not in close relationship with the clinical course of the disease and the associated comorbidities. The present study was aimed at identifying metabolites that could be used as biomarkers for a better disease phenotyping. For this purpose, metabolic fingerprint using an untargeted metabolomic approach was examined in serum from 30 patients with acromegaly and 30 age-matched controls. Patients with acromegaly presented fewer branched-chain amino acids (BCAAs) compared to the control group (valine: 4. 75 ± 0. 87 vs. 5. 20 ± 1. 06 arbitrary units (AUs), p < 0. 05; isoleucine: 2. 54 ± 0. 41 vs. 2. 80 ± 0. 51 AUs; p < 0. 05). BCAAs were also lower in patients with active disease compared to patients with normal levels of IGF-1 with or without medical treatment. GH, but not IGF-1, serum levels were inversely correlated with both valine and isoleucine. These findings indicate that low levels of BCAAs represent the main metabolic fingerprint of acromegaly and that GH, rather than IGF-1, might be the primary mediator. In addition, our results suggest that the assessment of BCAAs could help to identify active disease and to monitor the response to therapeutic strategies. |
| Ajuts: |
Agencia Estatal de Investigación BFU2016-80360-R Ministerio de Economía y Competitividad PI16/00264 Ministerio de Economía y Competitividad CP15/00156
|
| Drets: |
Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original.  |
| Llengua: |
Anglès |
| Document: |
Article ; recerca ; Versió publicada |
| Matèria: |
Acromegaly ;
Metabolomics ;
Amino acids ;
Branched chain ;
Insulin resistance ;
Muscular weakness |
| Publicat a: |
Journal of clinical medicine, Vol. 8 (september 2019) , ISSN 2077-0383 |
DOI: 10.3390/jcm8101549
PMID: 31561638
El registre apareix a les col·leccions:
Articles >
Articles de recercaArticles >
Articles publicats
Registre creat el 2022-02-07, darrera modificació el 2026-02-15