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Lebenthal, Yael

0000-0001-5963-0574

Mayo Clinic

Pediatric Endocrinology and Diabetes Unit, Dana-Dwek Children's Hospital , Tel Aviv 6423906 ,

Citations 1

Lipodystrophy Severity Score to Assess Disease Burden in Lipodystrophy
Brown, Rebecca J. , Akıncı, Barış , Yosef, Matheos , Phillips, Helen , Khalatbari, Shokoufeh , Santini, Ferruccio , Brush, Maiah, Meral, Rasimcan , Prodam, Flavia , Schnurbein, Julia von , Sorice, Gian Pio , Güler, Merve Çelik , Patni, Nivedita , Tanrıkulu, Seher , Ozgen, Basak S, Foss‐Freitas, Maria Cristina , Özışık, Seçil , Segrestin, Bérénice , Özcan, Büşra, Adıyaman, Süleyman Cem , Musolino, Gianluca , Sekizkardes, Hilal , Musso, Carla , Simha, Vinaya , Stears, Anna, Gambineri, Alessandra , Semple, Robert K. , Prodam, Flavia , von Schnurbein, Julia , Sekizkardes, Hilal , Lebenthal, Yael , Simha, Vinaya , Wabitsch, Martin , Oral, Elif A , Brown, Rebecca J. , Sorkina, Ekaterina , Vigouroux, Corinne , Ceccarini, Giovanni , Zeybel, Müjdat , Al-Yaarubi, Saif , Ozgen, Basak S, Özen, Samim , Şimşir, İlgın Yıldırım , Scherer, Thomas , Lima, Josivan Gomes , Araújo‐Vilar, David , Hegele, Robert Alexander , Oral, Elif A

The Journal of Clinical Endocrinology & Metabolism | February 19, 2025 | Volume: 110 | Issue: 11 | Pages: 3243-3255

10.1210/clinem/dgaf103 Get It

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 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.