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The role of adipose tissue secretion in the creation and pain level in osteoarthritis.

Authors :
Askari A
Arasteh P
Homayounfar R
Naghizadeh MM
Ehrampoush E
Mousavi SM
Alipoor R
Source :
Endocrine regulations [Endocr Regul] 2020 Jan 01; Vol. 54 (1), pp. 6-13.
Publication Year :
2020

Abstract

Objectives: With increasing evidence regarding the metabolic basis of osteoarthritis (OA), we studied the relationship between adipose tissue and OA.<br />Methods: This study is part of an OA registry in the eastern part of Fars Province, Iran. Overall, 150 patients with OA and 300 sex matched individuals were selected as a control group. They were compared regarding adipokine concentration (leptin, adiponectin, resistin and visfatin), anthropo-metric indices, the Western Ontario and McMaster universities arthritis index score (WOMAC).<br />Results: All adipokine levels were higher among OA patients (p<0.001). After adjusting for age, sex, and body mass index (BMI), adipokines showed a significant and positive association with OA (B: 14.12, B: 9.92, B: 24.71 and B: 12.29 for leptin, adiponectin, visfatin, and resistin, respectively; p<0.001). Except the adiponectin that had a negative relationship with BMI in the OA group (r=-0.570, p<0.001), other adipokines had positive relationships with BMI (r=0.781, p<0.001; r=0.530, p<0.001; r=0.549, p<0.001 for leptin, visfatin, and resistin, respectively). Only leptin and adiponectin levels were correlated with pain (B: 0.045, -0.079 and p<0.05).<br />Conclusion: The present study shows that aside to the well-known role of mechanical stress in OA pathogenesis (weight load), leptin, adiponectin, visfatin, and resistin, which represent the adi-pose tissue independent on the weight, may play a chemical role in OA pathogenesis. In addition, leptin and adiponectin may be involved in the pain levels among patients with OA.

Details

Language :
English
ISSN :
1336-0329
Volume :
54
Issue :
1
Database :
MEDLINE
Journal :
Endocrine regulations
Publication Type :
Academic Journal
Accession number :
32597150
Full Text :
https://doi.org/10.2478/enr-2020-0002