Irisin levels in LMNA-associated partial lipodystrophies.
Absorptiometry, Photon
Adult
Blood Glucose
Body Composition
/ physiology
Body Mass Index
Case-Control Studies
Female
Fibronectins
/ blood
Humans
Insulin
/ blood
Lamin Type A
/ genetics
Leptin
/ blood
Lipodystrophy, Familial Partial
/ blood
Magnetic Resonance Imaging
Male
Middle Aged
Obesity
/ blood
Triglycerides
/ blood
Young Adult
Fat mass
Irisin
Lamin A
Lean mass
Leptin
Lipodystrophy
Journal
Diabetes & metabolism
ISSN: 1878-1780
Titre abrégé: Diabetes Metab
Pays: France
ID NLM: 9607599
Informations de publication
Date de publication:
01 2019
01 2019
Historique:
received:
01
05
2017
revised:
22
07
2018
accepted:
16
08
2018
pubmed:
31
8
2018
medline:
22
6
2019
entrez:
31
8
2018
Statut:
ppublish
Résumé
The adipo-myokine irisin regulates energy expenditure and fat metabolism. LMNA-associated familial partial lipodystrophy (FPLD2) comprises insulin resistance, muscle hypertrophy and lipoatrophy. The aim of this study was to investigate whether irisin could be a biomarker of FPLD2. This case control study included 19 FPLD2 subjects, 13 obese non-diabetic (OND) patients and 19 healthy controls (HC) of normal weight (median BMI: 26, 39 and 22 kg/m BMI and MRI intra-abdominal fat significantly differed among these three groups, whereas DXA total fat mass and leptin levels were higher in the OND group, but did not differ between HC and FPLD2. Lipodystrophy patients had higher intra-abdominal/total abdominal fat ratios than the other two groups. Irisin levels were higher in FPLD2 and OND patients than in HC (medians: 944, 934 and 804 ng/mL, respectively). However, irisin/leptin ratios and lean body mass percentages were strikingly higher, and lean mass indices lower, in FPLD2 and HC than in the OND (median irisin/leptin ratios: 137, 166 and 21, respectively). In the entire study group, irisin levels positively correlated with BMI, lean body mass and index, intra-abdominal/total abdominal fat ratio, triglyceride, cholesterol, insulin, glucose and HbA Circulating irisin is similarly increased in FPLD2 and OND patients, who are characterized by higher lean body mass regardless of their clearly different fat mass. However, irisin/leptin ratios, strikingly higher in FPLD2 than in OND patients, could help to make the diagnosis and prompt genetic testing in clinically atypical cases.
Identifiants
pubmed: 30165155
pii: S1262-3636(18)30160-5
doi: 10.1016/j.diabet.2018.08.003
pii:
doi:
Substances chimiques
Blood Glucose
0
FNDC5 protein, human
0
Fibronectins
0
Insulin
0
LMNA protein, human
0
Lamin Type A
0
Leptin
0
Triglycerides
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
67-75Informations de copyright
Copyright © 2018. Published by Elsevier Masson SAS.