Adipokines and bone status in a cohort of ...
Document type :
Article dans une revue scientifique: Article original
PMID :
Permalink :
Title :
Adipokines and bone status in a cohort of anorexic patients.
Author(s) :
Legroux-Gérot, Isabelle [Auteur]
Marrow Adiposity & Bone Lab - Adiposité Médullaire et Os - ULR 4490 [MABLab]
Vignau, Jean [Auteur]
Viltart, Odile [Auteur]
Centre de Recherche Jean-Pierre AUBERT Neurosciences et Cancer - U837 [JPArc]
Hardouin, Pierre [Auteur]
Marrow Adiposity & Bone Lab (MABLab) - ULR 4490
Chauveau, Christophe [Auteur]
Marrow Adiposity & Bone Lab (MABLab) - ULR 4490
Cortet, Bernard [Auteur]
Marrow Adiposity & Bone Lab (MABLab) - ULR 4490
Marrow Adiposity & Bone Lab - Adiposité Médullaire et Os - ULR 4490 [MABLab]
Vignau, Jean [Auteur]
Viltart, Odile [Auteur]
Centre de Recherche Jean-Pierre AUBERT Neurosciences et Cancer - U837 [JPArc]
Hardouin, Pierre [Auteur]
Marrow Adiposity & Bone Lab (MABLab) - ULR 4490
Chauveau, Christophe [Auteur]
Marrow Adiposity & Bone Lab (MABLab) - ULR 4490
Cortet, Bernard [Auteur]
Marrow Adiposity & Bone Lab (MABLab) - ULR 4490
Journal title :
Joint Bone Spine
Abbreviated title :
Joint Bone Spine
Volume number :
86
Pages :
95-101
Publication date :
2019-01-01
ISSN :
1778-7254
English keyword(s) :
Absorptiometry, Photon
Adiponectin
Adolescent
Adult
Anorexia
Body Mass Index
Bone Density
Bone Diseases, Metabolic
Calcium-Binding Proteins
Cohort Studies
Female
Femur Neck
Humans
Leptin
Membrane Proteins
Osteoporosis
Young Adult
Adipokines
Adiponectin
Anorexia nervosa
Bone mineral density
Leptin
Pref-1
Adiponectin
Adolescent
Adult
Anorexia
Body Mass Index
Bone Density
Bone Diseases, Metabolic
Calcium-Binding Proteins
Cohort Studies
Female
Femur Neck
Humans
Leptin
Membrane Proteins
Osteoporosis
Young Adult
Adipokines
Adiponectin
Anorexia nervosa
Bone mineral density
Leptin
Pref-1
English abstract : [en]
Bone loss in anorexia nervosa (AN) is multifactorial; its mechanisms are not yet clearly understood and may vary depending on disease duration and severity. To determine to what extent adipokines may be involved in the ...
Show more >Bone loss in anorexia nervosa (AN) is multifactorial; its mechanisms are not yet clearly understood and may vary depending on disease duration and severity. To determine to what extent adipokines may be involved in the bone alterations found in anorexic patients, we evaluated plasma levels for leptin, adiponectin and Pref-1 against other clinical and biological parameters in a population of anorexic patients split according to weight and bone status. Plasma concentrations of leptin, total adiponectin, high molecular weight (HMW) adiponectin, and Pref-1 were measured. The ratio of HMW adiponectin to total adiponectin - HMW (percentage) - was calculated. We divided our population into 5 groups with different phenotypes characterizing the severity of the disease and/or the severity of bone involvement: 1 - Normal BMD and body mass index (BMI): recovery from AN; 2 - Osteopenia (-217kg/m; 3 - Osteopenia and BMI≤17kg/m; 4 - Osteoporosis (Z-score≤-2) and BMI>17kg/m; 5 - Osteoporosis and BMI≤17kg/m. The study involved 80 anorexia nervosa patients. Mean BMI was 16.8±2.4kg/m. No significant difference was found in total and HMW adiponectin plasma concentrations between the 5 groups. HMW (percentage) was significantly higher in group 5 compared to group 1. Leptin was significantly lower in groups 3 and 5 compared to the other groups. For the whole group femoral neck and hip BMD correlated negatively with total adiponectin and HMW adiponectin. No correlation was found between BMD (whatever the site) and plasma leptin. Multivariate analysis revealed that 2 factors - leptin and BMI - explained 10% of the variance in spine BMD. For femoral neck BMD, the 2 explanatory factors were BMI and total adiponectin which explained 14% of the variance in BMD. For total hip BMD, 27% of the variance in BMD was explained by 3 factors: leptin, BMI, and total adiponectin. Bone status in anorexia nervosa is mainly determined by BMI, leptin and adiponectin.Show less >
Show more >Bone loss in anorexia nervosa (AN) is multifactorial; its mechanisms are not yet clearly understood and may vary depending on disease duration and severity. To determine to what extent adipokines may be involved in the bone alterations found in anorexic patients, we evaluated plasma levels for leptin, adiponectin and Pref-1 against other clinical and biological parameters in a population of anorexic patients split according to weight and bone status. Plasma concentrations of leptin, total adiponectin, high molecular weight (HMW) adiponectin, and Pref-1 were measured. The ratio of HMW adiponectin to total adiponectin - HMW (percentage) - was calculated. We divided our population into 5 groups with different phenotypes characterizing the severity of the disease and/or the severity of bone involvement: 1 - Normal BMD and body mass index (BMI): recovery from AN; 2 - Osteopenia (-217kg/m; 3 - Osteopenia and BMI≤17kg/m; 4 - Osteoporosis (Z-score≤-2) and BMI>17kg/m; 5 - Osteoporosis and BMI≤17kg/m. The study involved 80 anorexia nervosa patients. Mean BMI was 16.8±2.4kg/m. No significant difference was found in total and HMW adiponectin plasma concentrations between the 5 groups. HMW (percentage) was significantly higher in group 5 compared to group 1. Leptin was significantly lower in groups 3 and 5 compared to the other groups. For the whole group femoral neck and hip BMD correlated negatively with total adiponectin and HMW adiponectin. No correlation was found between BMD (whatever the site) and plasma leptin. Multivariate analysis revealed that 2 factors - leptin and BMI - explained 10% of the variance in spine BMD. For femoral neck BMD, the 2 explanatory factors were BMI and total adiponectin which explained 14% of the variance in BMD. For total hip BMD, 27% of the variance in BMD was explained by 3 factors: leptin, BMI, and total adiponectin. Bone status in anorexia nervosa is mainly determined by BMI, leptin and adiponectin.Show less >
Language :
Anglais
Peer reviewed article :
Oui
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Université de Lille
CNRS
CHU Lille
CNRS
CHU Lille
Collections :
Submission date :
2024-01-10T15:08:23Z
2024-01-10T17:47:54Z
2024-01-10T17:47:54Z
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