Irisin levels in LMNA-associated partial lipodystrophies.


Journal

Diabetes & metabolism
ISSN: 1878-1780
Titre abrégé: Diabetes Metab
Pays: France
ID NLM: 9607599

Informations de publication

Date de publication:
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

67-75

Informations de copyright

Copyright © 2018. Published by Elsevier Masson SAS.

Auteurs

F Bensmaïne (F)

Department of endocrinology and metabolism, Lille university hospital, 59037 Lille, France.

K Benomar (K)

Department of endocrinology and metabolism, Lille university hospital, 59037 Lille, France.

S Espiard (S)

Department of endocrinology and metabolism, Lille university hospital, 59037 Lille, France.

C Vahe (C)

Department of endocrinology and metabolism, Lille university hospital, 59037 Lille, France.

K Le Mapihan (K)

Department of endocrinology and metabolism, Lille university hospital, 59037 Lille, France.

G Lion (G)

Department of nuclear medicine, Lille university hospital, 59037 Lille, France.

M Lemdani (M)

Department of public health, university Lille EA 2694, 59000 Lille, France.

E Chazard (E)

Department of public health, university Lille EA 2694, 59000 Lille, France.

O Ernst (O)

Department of radiology, Lille university hospital, 59037 Lille France.

C Vigouroux (C)

Inserm UMR_S938, departments of endocrinology and molecular biology and genetics, Saint-Antoine hospital, Saint-Antoine research centre, Sorbonne université, Assistance publique-Hôpitaux de Paris (AP-HP), 75012 Paris, France; Institute of cardiometabolism and nutrition (ICAN), 75013 Paris, France; National reference centre of rare diseases of insulin secretion and of insulin sensitivity, hospital Saint-Antoine, 75012 Paris, France.

P Pigny (P)

Department of biology, Lille university hospital, 59037 Lille France.

M-C Vantyghem (MC)

Department of endocrinology and metabolism, Lille university hospital, 59037 Lille, France; National reference centre of rare diseases of insulin secretion and of insulin sensitivity, hospital Saint-Antoine, 75012 Paris, France; Inserm U1190, European genomic institute for diabetes, 59000 Lille, France. Electronic address: mc-vantyghem@chru-lille.fr.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH