AimsThis 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.MethodsSix 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 18F-FDG PET/CT scans; hypothalamic gliosis was determined using MRI scans; blood was collected for hormone and biochemistry measurements. All tests were performed at inclusion and six months after pioglitazone introduction.ResultsPioglitazone 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.ConclusionsThis 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.

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 / J.C. De‑lima‑júnior, S. Rodovalho, S. Van de Sande‑Lee, M.M. ·, B. Rachid, R.M. Cintra, C.D. Ramos, F. Cendes, F. Folli, L.A. Velloso. - In: ACTA DIABETOLOGICA. - ISSN 0940-5429. - 56:12(2019 Dec 01), pp. 1333-1339. [10.1007/s00592-019-01418-2]

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

F. Folli
Penultimo
Writing – Original Draft Preparation
;
2019

Abstract

AimsThis 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.MethodsSix 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 18F-FDG PET/CT scans; hypothalamic gliosis was determined using MRI scans; blood was collected for hormone and biochemistry measurements. All tests were performed at inclusion and six months after pioglitazone introduction.ResultsPioglitazone 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.ConclusionsThis 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.
English
insulin resistance; Glucose intolerance; obesity; hypothalamus; brown adipose tissue
Settore MED/09 - Medicina Interna
Articolo
Esperti anonimi
Ricerca applicata
Pubblicazione scientifica
1-dic-2019
10-set-2019
Springer
56
12
1333
1339
7
Pubblicato
Periodico con rilevanza internazionale
Aderisco
info:eu-repo/semantics/article
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 / J.C. De‑lima‑júnior, S. Rodovalho, S. Van de Sande‑Lee, M.M. ·, B. Rachid, R.M. Cintra, C.D. Ramos, F. Cendes, F. Folli, L.A. Velloso. - In: ACTA DIABETOLOGICA. - ISSN 0940-5429. - 56:12(2019 Dec 01), pp. 1333-1339. [10.1007/s00592-019-01418-2]
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J.C. De‑lima‑júnior, S. Rodovalho, S. Van de Sande‑Lee, M.M. ·, B. Rachid, R.M. Cintra, C.D. Ramos, F. Cendes, F. Folli, L.A. Velloso...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/674607
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