脂肪营养不良严重程度评分评估脂肪营养不良患者的疾病负担。

IF 5.1 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Rebecca J Brown, Baris Akinci, Matheos Yosef, Helen Phillips, Shokoufeh Khalatbari, Ekaterina Sorkina, Ferruccio Santini, Corinne Vigouroux, Maiah Brush, Rasimcan Meral, Giovanni Ceccarini, Mujdat Zeybel, Flavia Prodam, Julia von Schnurbein, Gian P Sorice, Merve C Guler, Nivedita Patni, Seher Tanrikulu, Saif Alyaarubi, Basak S Ozgen, Maria C Foss-Freitas, Secil Ozisik, Benerice Segrestin, Busra Ozcan, Suleyman C Adiyaman, Gianluca Musolino, Hilal Sekizkardes, Carla Musso, Yael Lebenthal, Samim Ozen, Vinaya Simha, Ilgin Y Simsir, Anna Stears, Thomas Scherer, Alessandra Gambineri, Josivan G Lima, Robert Semple, Martin Wabitsch, David Araujo-Vilar, Robert A Hegele, Elif A Oral
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引用次数: 0

摘要

背景:脂肪营养不良综合征是一种罕见的以脂肪组织缺乏为特征的疾病,可导致胰岛素抵抗、血脂异常和器官系统异常。目的:我们的目标是开发一种脂肪营养不良严重程度评分(LDS),以全面捕捉脂肪营养不良的各种表现为数值评分,以帮助预测临床结果和/或治疗效果。设计:8位疾病专家与患者组织协商制定了8域LDS。另外28名临床医生和9名患者代表对LDS的可行性和内容效度进行了评估。在两个不同的时间点,将LDS与20个假定患者的严重程度的临床总体印象(CGI)进行比较,并将LDS的变化与总体印象的变化进行比较。为了进行外部验证,计算了两组接受美曲瘦素治疗的脂肪营养不良患者的LDS。结果:LDS领域包括糖尿病/胰岛素抵抗、糖尿病微血管并发症、血脂、心血管、肝脏、肾脏、生殖和其他。每个领域通过一个或多个问题来评估脂肪营养不良的终生和近期并发症。通过类内相关系数分析,LDS具有较高的内容效度和可行性,信度较高(>0.95)。总体和领域特异性LDS与CGI密切相关,各次访问评分的变化也与CGI密切相关(R=0.79-0.99)。结论:LDS可以反映脂肪营养不良各种表现的严重程度,并监测干预后的变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lipodystrophy Severity Score to Assess Disease Burden in Lipodystrophy.

Context: Lipodystrophy syndromes are rare disorders characterized by deficient adipose tissue, leading to insulin resistance, dyslipidemia, and organ system abnormalities.

Objective: Our goal was to develop a lipodystrophy severity score (LDS) to holistically capture the diverse manifestations of lipodystrophy into a numerical score to aid in prediction of clinical outcomes and/or treatment impact.

Design: An 8-domain LDS was developed by 8 disease experts in consultation with patient organizations. The LDS was rated for feasibility and content validity by 28 additional clinicians and 9 patient representatives. LDS was compared to the Clinical Global Impression (CGI) of severity for 20 putative patient profiles, each at 2 different time points, and by comparing change in LDS to global impression of change. For external validation, LDS was calculated in 2 cohorts of patients with lipodystrophy treated with metreleptin.

Results: LDS domains include Diabetes/Insulin Resistance, Microvascular Complications of Diabetes, Lipids, Cardiovascular, Liver, Kidney, Reproductive, and Other. Each domain is assessed by 1 or more questions assessing both lifetime and recent complications of lipodystrophy. The LDS had high content validity and feasibility and high reliability by intraclass correlation coefficients (>0.95). Global and domain-specific LDS were strongly correlated with CGI, as were changes in scores across visits (R = 0.79-0.99, P < .001 for all). In generalized lipodystrophy, metreleptin significantly reduced LDS (from 46 to 26 at 12 months, P < .001). The reductions were smaller in partial lipodystrophy (from 65 to 61 at 12 months, P = .04).

Conclusion: The LDS can reflect the severity of diverse manifestations of lipodystrophy and monitor changes following interventions.

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来源期刊
Journal of Clinical Endocrinology & Metabolism
Journal of Clinical Endocrinology & Metabolism 医学-内分泌学与代谢
CiteScore
11.40
自引率
5.20%
发文量
673
审稿时长
1 months
期刊介绍: The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.
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