Serum Leptin, Resistin, and Adiponectin Concentrations in Psoriasis: A Meta-Analysis of Observational Studies

被引:77
作者
Kyriakou, Aikaterini [1 ]
Patsatsi, Aikaterini [1 ]
Sotiriadis, Dimitrios [1 ]
Goulis, Dimitrios G. [2 ]
机构
[1] Aristotle Univ Thessaloniki, Med Sch, Dept Dermatol & Venereol 2, Thessaloniki, Greece
[2] Aristotle Univ Thessaloniki, Med Sch, Dept Obstet & Gynecol 1, Unit Reprod Endocrinol, Thessaloniki, Greece
关键词
Leptin; Resistin; Adiponectin; Psoriasis; Adipokines; Meta-analysis; NECROSIS-FACTOR-ALPHA; BODY-MASS INDEX; ADIPOSE-TISSUE; INSULIN-RESISTANCE; METABOLIC SYNDROME; ADIPOKINE LEVELS; PLASMA ADIPONECTIN; OBESITY; INFLAMMATION; ASSOCIATION;
D O I
10.1159/000481882
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Psoriasis is an immune-mediated, inflammatory disease. Adipokines contribute to the regulation of immune-mediated processes and inflammation. Objective: The aim of our study was to systematically review the literature for studies that have evaluated the circulating concentrations of adipokines in patients with psoriasis and controls and to meta-analyze the best evidence available. Methods: Eligible were studies that have assessed leptin, resistin, or adiponectin concentrations in psoriatic patients and a reference group. The study was conducted in adherence with the PRISMA standards. Results: Psoriatic patients had higher leptin concentrations compared to controls (random effects model, mean difference, MD = 5.64 ng/mL, 95% CI: 3.00-8.29, p < 0.0001). Heterogeneity among studies was high (I-2 = 95.9%). Psoriatic patients had higher resistin concentrations compared to controls (MD = 4.66 ng/mL, 95% CI: 2.62-6.69, p < 0.0001). Heterogeneity was high (I-2 = 99.2%). Finally, psoriatic patients had lower adiponectin concentrations compared to controls (MD = -1.87 mu g/mL, 95% CI: -2.76 to -0.98, p < 0.0001). Heterogeneity was high (I-2 = 95.9%). Conclusion: The study supported the hypothesis that leptin and resistin concentrations are higher and adiponectin concentrations are lower in patients with psoriasis compared to controls. Hereby, the suggested pathogenic link between psoriasis and metabolic syndrome/obesity is reinforced and the role of comorbidities in psoriasis is highlighted. (c) 2017 S. Karger AG, Basel
引用
收藏
页码:378 / 389
页数:12
相关论文
共 69 条
[1]   Clinical and laboratory parameters associated with metabolic syndrome in Turkish patients with psoriasis [J].
Akcali, Cenk ;
Buyukcelik, Burcin ;
Kirtak, Necmettin ;
Inaloz, Serhat .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2014, 42 (02) :386-394
[2]  
[Anonymous], 2001, SYSTEMATIC REV HLTH
[3]  
Asha Kumari, 2014, Acta Medica (Hradec Kralove), V57, P21
[4]   Adipose tissue and its relation to inflammation:: The role of adipokines [J].
Axelsson, J ;
Heimbürger, O ;
Lindholm, B ;
Stenvinkel, P .
JOURNAL OF RENAL NUTRITION, 2005, 15 (01) :131-136
[5]   The correlation between adiposity and adiponectin tumor necrosis factor α, interleukin-6 and high sensitivity C-reactive protein levels.: Is adipocyte size asssociated with inflammation in adults? [J].
Bahceci, M. ;
Gokalp, D. ;
Bahceci, S. ;
Tuzcu, A. ;
Atmaca, S. ;
Arikan, S. .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2007, 30 (03) :210-214
[6]   Serum adiponectin and leptin levels in psoriatic patients according to topical treatment [J].
Baran, A. ;
Flisiak, I. ;
Jaroszewicz, J. ;
Swiderska, M. .
JOURNAL OF DERMATOLOGICAL TREATMENT, 2015, 26 (02) :134-138
[8]   The 'psoriatic march': a concept of how severe psoriasis may drive cardiovascular comorbidity [J].
Boehncke, Wolf-Henning ;
Boehncke, Sandra ;
Tobin, Anne-Marie ;
Kirby, Brian .
EXPERIMENTAL DERMATOLOGY, 2011, 20 (04) :303-307
[9]  
Boehncke Wolf-Henning, 2011, J Rheumatol, V38, P567, DOI 10.3899/jrheum.101124
[10]   Serum levels of adipocytokines in psoriasis patients receiving tumor necrosis factor-α inhibitors: results of a retrospective analysis [J].
Campanati, Anna ;
Ganzetti, Giulia ;
Giuliodori, Katia ;
Marra, Maurizio ;
Bonfigli, Annarita ;
Testa, Roberto ;
Offidani, Annamaria .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2015, 54 (07) :839-845