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胰岛素抵抗性肥胖相关黑棘皮病的治疗选择

Treatment options in insulin resistance obesity-related acanthosis nigricans.

作者信息

Romo Anthony, Benavides Sandra

机构信息

College of Pharmacy, University of Texas at Austin, Austin, TX, USA.

出版信息

Ann Pharmacother. 2008 Jul;42(7):1090-4. doi: 10.1345/aph.1K446. Epub 2008 May 20.

Abstract

OBJECTIVE

To evaluate the literature to determine which oral and topical medications are most effective in the treatment of insulin resistance obesity-related acanthosis nigricans (IRORAN).

DATA SOURCES

A MEDLINE literature search was conducted (1950-January 2008) using the search terms acanthosis nigricans (AN), metformin, rosiglitazone, octreotide, retinoic acid, acitretin, etretinate, and isotretinoin. The search was limited to articles on treatment of IRORAN in humans written in the English language. Articles were retrieved and all references were reviewed.

STUDY SELECTION AND DATA EXTRACTION

Articles selected for inclusion were limited to AN related to obesity with no other underlying etiology. Clinical trials and case reports using monotherapy were included.

DATA SYNTHESIS

Metformin, rosiglitazone, octreotide, vitamin D analogs, and retinoic acid have been used in the treatment of IRORAN. In one randomized trial, metformin 500 mg 3 times daily was compared with rosiglitazone 4 mg once daily. Neither treatment demonstrated significant improvements in AN; however, rosiglitazone did significantly decrease serum insulin levels. In a second clinical trial and in several case reports, AN and hyperinsulinemia did show improvement with metformin treatment. After a 6-month period, octreotide improved IRORAN, body weight, and glucose/insulin response to a meal. The improvements persisted for 6 additional months after discontinuation of octreotide. Vitamin D analogs and retinoids produced inconsistent results in 5 separate case reports.

CONCLUSIONS

IRORAN is a growing problem, particularly in children and adolescents, secondary to the increase in the prevalence of obesity. Treatment of IRONAN should focus on reversal of the underlying hyperinsulinemia. Patients with IRORAN may benefit from a trial of metformin for improvement of lesions and underlying hyperinsulinemia.

摘要

目的

评估文献以确定哪些口服和外用药物在治疗胰岛素抵抗性肥胖相关黑棘皮病(IRORAN)方面最有效。

数据来源

利用搜索词“黑棘皮病(AN)”“二甲双胍”“罗格列酮”“奥曲肽”“维甲酸”“阿维A”“依曲替酯”和“异维A酸”进行了MEDLINE文献检索(1950年1月至2008年)。检索仅限于用英语撰写的关于人类IRORAN治疗的文章。检索出文章并对所有参考文献进行了审查。

研究选择和数据提取

入选的文章仅限于与肥胖相关且无其他潜在病因的黑棘皮病。纳入了使用单一疗法的临床试验和病例报告。

数据综合

二甲双胍、罗格列酮、奥曲肽、维生素D类似物和维甲酸已用于IRORAN的治疗。在一项随机试验中,将每日3次、每次500毫克的二甲双胍与每日1次、每次4毫克的罗格列酮进行了比较。两种治疗均未显示黑棘皮病有显著改善;然而,罗格列酮确实显著降低了血清胰岛素水平。在第二项临床试验和几篇病例报告中,二甲双胍治疗后黑棘皮病和高胰岛素血症确实有所改善。经过6个月的治疗期,奥曲肽改善了IRORAN、体重以及对一餐的血糖/胰岛素反应。停用奥曲肽后,改善情况又持续了6个月。在5篇单独的病例报告中,维生素D类似物和维甲酸产生了不一致的结果。

结论

IRORAN是一个日益严重的问题,尤其是在儿童和青少年中,这是肥胖患病率增加的继发问题。IRONAN的治疗应侧重于逆转潜在的高胰岛素血症。IRORAN患者可能会从试用二甲双胍改善皮损和潜在的高胰岛素血症中获益。

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