Effect of 40:1 myo-inositol/D-chiro-inositol treatment on serum asprosin levels in polycystic ovary syndrome: a prospective randomized pilot study.

IF 1
Ozlen Emekci Ozay, Yusuf Ozay, Oguzhan Edebal, Marco Calcagno, Ali Cenk Ozay
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Abstract

Objectives: Asprosin, a novel adipokine primarily secreted by white adipose tissue, has been implicated in the pathogenesis of insulin resistance and metabolic dysfunction. Its elevated levels characterize patients with polycystic ovary syndrome (PCOS) exhibiting metabolic alterations. Aim of this work was to evaluate the effects of insulin sensitizer administration, as inositols, on asprosin levels and then compare these results with the effects of metformin treatment.

Material and methods: 30 patients with PCOS were enrolled in this study and randomly divided into two groups: (i) group 1 assumed a dietary supplement based on 40:1 myo-inositol (MI)/D-chiro-inositol (DCI), (ii) group 2 assumed metformin (MET), for 12-16 weeks of treatment.

Results: The reduction of serum asprosin levels in patients with PCOS after treatment with MET and MI/DCI is the most intriguing result. Its levels decreased more in the inositol group, although they did not reach statistical significance probably due to the lower number of patients.

Conclusions: The observed dysregulation of asprosin levels in PCOS highlights a potential link between this novel adipokine and the pathophysiology of the disorder, suggesting a modulatory effect of the combined 40:1 MI/DCI on asprosin levels. Of course, further studies may contribute to disclosing molecular mechanisms underlying asprosin reduction and open toward new perspectives.

40:1肌肌醇/ d -肌肌醇治疗对多囊卵巢综合征血清asprosin水平的影响:一项前瞻性随机先导研究
目的:Asprosin是一种主要由白色脂肪组织分泌的新型脂肪因子,与胰岛素抵抗和代谢功能障碍的发病机制有关。其水平升高是多囊卵巢综合征(PCOS)患者表现出代谢改变的特征。这项工作的目的是评估胰岛素增敏剂(如肌醇)对asprosin水平的影响,然后将这些结果与二甲双胍治疗的效果进行比较。材料和方法:本研究纳入30例PCOS患者,随机分为两组:(i)组1服用40:1肌肌醇(MI)/ d -手性肌醇(DCI)膳食补充剂,(ii)组2服用二甲双胍(MET),治疗12-16周。结果:经MET和MI/DCI治疗后,PCOS患者血清asprosin水平的降低是最有趣的结果。它的水平在肌醇组下降得更多,尽管它们没有达到统计学意义,可能是由于患者人数较少。结论:在PCOS中观察到的asprosin水平失调突出了这种新型脂肪因子与疾病病理生理之间的潜在联系,表明40:1 MI/DCI对asprosin水平的调节作用。当然,进一步的研究可能有助于揭示asprosin还原的分子机制,并开辟新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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