Metformin Treatment of Hidradenitis Suppurativa: Effect on Metabolic Parameters, Inflammation, Cardiovascular Risk Biomarkers, and Immune Mediators

被引:16
作者
Hambly, Roisin [1 ,2 ]
Kearney, Niamh [1 ,2 ]
Hughes, Rosalind [1 ]
Fletcher, Jean M. [3 ,4 ]
Kirby, Brian [1 ,2 ]
机构
[1] St Vincents Univ Hosp, Charles Ctr, Dept Dermatol, Dublin D04T6F4, Ireland
[2] Univ Coll Dublin, Charles Inst Dermatol, Sch Med, Dublin D04V1W8, Ireland
[3] Trinity Coll Dublin, Trinity Biomed Sci Inst, Sch Biochem & Immunol, Dublin D02R590, Ireland
[4] Trinity Coll Dublin, Trinity Biomed Sci Inst, Sch Med, Dublin D02R590, Ireland
基金
英国惠康基金;
关键词
hidradenitis suppurativa; HS; metformin; insulin resistance; cardiovascular risk; adipokines; CRP; metabolic syndrome; POLYCYSTIC-OVARY-SYNDROME; TYPE-2; DIABETES-MELLITUS; ACTIVATED PROTEIN-KINASE; C-REACTIVE PROTEIN; T-HELPER; 17; INSULIN-RESISTANCE; WAIST CIRCUMFERENCE; WEIGHT-LOSS; ASSOCIATION; PREVALENCE;
D O I
10.3390/ijms24086969
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hidradenitis suppurativa (HS) is a common cutaneous and systemic inflammatory disease with a significant impact on mental health and quality of life. It is associated with obesity, insulin resistance, metabolic syndrome, cardiovascular (CV) disease, and increased all-cause mortality. Metformin is used frequently in HS treatment and is effective for some patients. The mechanism of action of metformin in HS is unknown. A case-control study of 40 patients with HS (20 on metformin and 20 controls) was conducted to assess differences in metabolic markers, inflammation (C-reactive protein [CRP], serum adipokines, and CV risk biomarkers), and serum immune mediators. Body mass index (BMI), insulin resistance (77%), and metabolic syndrome (44%) were high overall, but not significantly different between the groups. This highlights the need for co-morbidity screening and management. A significant reduction in fasting insulin and a trend towards a reduction in insulin resistance were identified in the metformin group compared with pre-treatment levels. CV risk biomarkers were significantly favourable in the metformin group (lymphocytes, monocyte-lymphocyte ratio, neutrophil-lymphocyte ratio, and platelet-lymphocyte ratio). CRP was lower in the metformin group but was not statistically significant. Adipokines were dysregulated overall but were not different between the two groups. Serum IFN-gamma, IL-8, TNF-alpha, and CXCL1 trended lower in the metformin group but did not reach significance. These results suggest that metformin improves CV risk biomarkers and insulin resistance in patients with HS. When the results of this study are considered alongside other studies in HS and related conditions, it is likely that metformin also has beneficial effects on metabolic markers and systemic inflammation in HS (CRP, serum adipokines, and immune mediators), warranting further research.
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页数:19
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