Effect of pioglitazone treatment on brown adipose tissue volume and activity and hypothalamic gliosis in patients with type 2 diabetes mellitus: a proof-of-concept study.


Journal

Acta diabetologica
ISSN: 1432-5233
Titre abrégé: Acta Diabetol
Pays: Germany
ID NLM: 9200299

Informations de publication

Date de publication:
Dec 2019
Historique:
received: 29 05 2019
accepted: 29 08 2019
pubmed: 12 9 2019
medline: 14 1 2020
entrez: 12 9 2019
Statut: ppublish

Résumé

This study aimed to evaluate the effect of pioglitazone on brown adipose tissue function and hypothalamic gliosis in humans. Brown adipose tissue and the hypothalamus are regarded as important potential pharmacological targets to metabolic diseases, and defining the impact of current therapies on their structure and/or function could provide therapeutic advance in this field. Six patients with type 2 diabetes were treated for 24 weeks with pioglitazone 30 mg/day as an add-on therapy. Brown adipose tissue glucose uptake and volume were determined using Pioglitazone treatment led to a significant 3% body mass increase. There were neither changes in cold-induced brown adipose tissue glucose uptake and volume nor changes in hypothalamic gliosis. This is a proof-of-concept study that provides clinical evidence for a lack of action of a thiazolidinedione, pioglitazone, to promote homogeneous and measurable changes in brown adipose tissue volume and also in hypothalamic gliosis after 6 months of treatment.

Identifiants

pubmed: 31506721
doi: 10.1007/s00592-019-01418-2
pii: 10.1007/s00592-019-01418-2
doi:

Substances chimiques

Thiazolidinediones 0
Fluorodeoxyglucose F18 0Z5B2CJX4D
2,4-thiazolidinedione AA68LXK93C
Pioglitazone X4OV71U42S

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1333-1339

Subventions

Organisme : Fundação de Amparo à Pesquisa do Estado de São Paulo
ID : 2013/07607-8

Auteurs

José C de-Lima-Júnior (JC)

Laboratory of Cell Signaling, Department of Internal Medicine, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
Obesity and Comorbidities Research Center, Campinas, São Paulo, Brazil.

Sylka Rodovalho (S)

Laboratory of Cell Signaling, Department of Internal Medicine, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
Obesity and Comorbidities Research Center, Campinas, São Paulo, Brazil.

Simone Van de Sande-Lee (S)

Laboratory of Cell Signaling, Department of Internal Medicine, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
Department of Internal Medicine, Federal University of Santa Catarina (UFSC), Florianópolis, SC, Brazil.

Milena Monfort-Pires (M)

Laboratory of Cell Signaling, Department of Internal Medicine, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
Obesity and Comorbidities Research Center, Campinas, São Paulo, Brazil.

Briana Rachid (B)

Laboratory of Cell Signaling, Department of Internal Medicine, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil.
Obesity and Comorbidities Research Center, Campinas, São Paulo, Brazil.

Riobaldo M Cintra (RM)

Obesity and Comorbidities Research Center, Campinas, São Paulo, Brazil.

Celso D Ramos (CD)

Department of Radiology, University of Campinas, Campinas, São Paulo, 13084-970, Brazil.

Fernando Cendes (F)

Neuroimaging Laboratory, Department of Neurology, University of Campinas, Campinas, Brazil.

Franco Folli (F)

Obesity and Comorbidities Research Center, Campinas, São Paulo, Brazil.
School of Medicine, Endocrinology and Metabolism Dipartimento di Scienze Della Salute, Universita' degli Studi di Milano, Milan, Italy.
Departmental Unit of Diabetes and Metabolic Disorders, Azienda Socio-Sanitaria Santi Paolo e Carlo, Via A. Di Rudini, 8, 20143, Milan, Italy.

Lício A Velloso (LA)

Laboratory of Cell Signaling, Department of Internal Medicine, University of Campinas (UNICAMP), Campinas, São Paulo, Brazil. lavelloso@fcm.unicamp.br.
Obesity and Comorbidities Research Center, Campinas, São Paulo, Brazil. lavelloso@fcm.unicamp.br.

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Classifications MeSH