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
Abstract
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 eight 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 Clinical Global Impression (CGI) of severity for 20 putative patient profiles, each at two different time points, and by comparing change in LDS to global impression of change. For external validation, LDS was calculated in two 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 one 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<0.001 for all). In generalized lipodystrophy, metreleptin significantly reduced LDS (from 46 to 26 at 12 months, P<0.001). The reductions were smaller in partial lipodystrophy (from 65 to 61 at 12 months, P=0.04).
Conclusions: The LDS can reflect the severity of diverse manifestations of lipodystrophy and monitor changes following interventions.
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.