Cross-sectional study using the University of California, Los Angeles, Scleroderma Clinical Trials Consortium Gastrointestinal Tract Instrument 2.0 (UCLA SCTC GIT 2.0) for gastrointestinal disorders of systemic sclerosis

IF 2.9 3区 医学 Q2 DERMATOLOGY
Satoko Hisada, Saki Takeuchi, Takahisa Tozawa, Yoshihiro Yamada, Yumi Ito, Masanari Kodera
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引用次数: 0

Abstract

This study aimed to identify severe gastrointestinal ailments in patients with systemic sclerosis (SSc), investigate the role of antibodies in gastrointestinal disorders, and explore the relationship between limited cutaneous SSc (lcSSc) and diffuse cutaneous SSc (dcSSc) in terms of gastrointestinal involvement and its association with skin stiffness. We used the University of California, Los Angeles, Scleroderma Clinical Trials Consortium Gastrointestinal Tract Instrument 2.0 (UCLA SCTC GIT 2.0) questionnaire to assess gastrointestinal disturbances in 100 patients with SSc. Gastrointestinal impairment was categorized into three levels: absence of or minor symptoms, moderate symptoms, and severe symptoms, as indicated by the total gastrointestinal tract (GIT) score. Comparing 27 patients with dcSSc and 73 patients with lcSSc, severe gastrointestinal disturbances were found in 7.4% of patients with dcSSc and 4.1% of patients with lcSSc. A total of 18.0% of anticentromere antibody (ACA)–positive patients exhibited moderate to severe symptoms, while 9.1% of antitopoisomerase 1 antibody–positive patients displayed similar symptoms. The average disease duration in patients with severe symptoms was 15.0 years, in those with moderate symptoms was 10.3 years, and in those who were symptom-free or mildly affected was 8.5 years. Among 16 patients with moderate to severe gastrointestinal disorders, a positive correlation was observed between the modified Rodnan skin thickness score (mRSS) and total GIT score. In addition, a positive correlation was identified between fecal incontinence and mRSS, with weaker correlations for reflux and bloating symptoms. Patients with gastrointestinal disorders showed a tendency to worsen over time, particularly in ACA-positive patients with dcSSc. Furthermore, a correlation was observed between mRSS and fecal incontinence, reflux, and abdominal bloating in patients with moderate to severe gastrointestinal disturbances.

使用加州大学洛杉矶分校硬皮病临床试验联盟胃肠道工具 2.0(UCLA SCTC GIT 2.0)对系统性硬化症的胃肠道疾病进行横断面研究。
本研究旨在确定系统性硬化症(SSc)患者的严重胃肠道疾病,调查抗体在胃肠道疾病中的作用,并探讨局限性皮肤SSc(lcSSc)和弥漫性皮肤SSc(dcSSc)在胃肠道受累方面的关系及其与皮肤僵硬度的关联。我们使用加州大学洛杉矶分校硬皮病临床试验联盟胃肠道工具 2.0(UCLA SCTC GIT 2.0)问卷评估了 100 名 SSc 患者的胃肠功能紊乱情况。胃肠道功能障碍分为三个等级:无症状或轻微症状、中度症状和重度症状,以胃肠道(GIT)总分表示。对 27 名 dcSSc 患者和 73 名 lcSSc 患者进行了比较,发现 7.4% 的 dcSSc 患者和 4.1% 的 lcSSc 患者出现了严重的胃肠功能紊乱。18.0%的抗中心粒抗体(ACA)阳性患者表现出中度至重度症状,9.1%的抗异构酶1抗体阳性患者表现出类似症状。重度症状患者的平均病程为 15.0 年,中度症状患者的平均病程为 10.3 年,无症状或轻度患者的平均病程为 8.5 年。在 16 名中重度胃肠功能紊乱患者中,改良罗德南皮肤厚度评分(mRSS)与胃肠道总评分之间呈正相关。此外,还发现大便失禁与 mRSS 呈正相关,反流和腹胀症状的相关性较弱。随着时间的推移,胃肠功能紊乱患者的病情有恶化的趋势,尤其是在 ACA 阳性的 dcSSc 患者中。此外,在中度至重度胃肠功能紊乱患者中,还观察到 mRSS 与大便失禁、反流和腹胀之间存在相关性。
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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来源期刊
Journal of Dermatology
Journal of Dermatology 医学-皮肤病学
CiteScore
4.60
自引率
9.70%
发文量
368
审稿时长
4-8 weeks
期刊介绍: The Journal of Dermatology is the official peer-reviewed publication of the Japanese Dermatological Association and the Asian Dermatological Association. The journal aims to provide a forum for the exchange of information about new and significant research in dermatology and to promote the discipline of dermatology in Japan and throughout the world. Research articles are supplemented by reviews, theoretical articles, special features, commentaries, book reviews and proceedings of workshops and conferences. Preliminary or short reports and letters to the editor of two printed pages or less will be published as soon as possible. Papers in all fields of dermatology will be considered.
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