Pelvis Magnetic Resonance Imaging to Diagnose Familial Partial Lipodystrophy

Author:

Adiyaman Suleyman Cem1ORCID,Altay Canan2ORCID,Kamisli Berfu Y3ORCID,Avci Emre Ruhat2ORCID,Basara Isil2ORCID,Simsir Ilgin Yildirim4ORCID,Atik Tahir5ORCID,Secil Mustafa2ORCID,Oral Elif A6ORCID,Akinci Baris7ORCID

Affiliation:

1. Division of Endocrinology and Metabolism, Department of Internal Medicine, Dokuz Eylul University School of Medicine , Izmir 35330 , Turkey

2. Department of Radiology, Dokuz Eylul University School of Medicine , Izmir 35330 , Turkey

3. Department of Internal Medicine, Dokuz Eylul University School of Medicine , Izmir 35330 , Turkey

4. Division of Endocrinology, Department of Internal Medicine, Ege University School of Medicine , Izmir 35030 , Turkey

5. Department of Pediatric Genetics, Ege University School of Medicine , Izmir 35030 , Turkey

6. Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine, University of Michigan , Ann Arbor, MI 48105 , USA

7. Depark, Dokuz Eylul University , Izmir 35330 , Turkey

Abstract

Abstract Context The diagnosis of familial partial lipodystrophy (FPLD) is currently made based on clinical judgment. Objective There is a need for objective diagnostic tools that can diagnose FPLD accurately. Methods We have developed a new method that uses measurements from pelvic magnetic resonance imaging (MRI) at the pubis level. We evaluated measurements from a lipodystrophy cohort (n = 59; median age [25th-75th percentiles]: 32 [24-44]; 48 females and 11 males) and age- and sex-matched controls (n = 29). Another dataset included MRIs from 289 consecutive patients. Results Receiver operating characteristic curve analysis revealed a potential cut-point of ≤13 mm gluteal fat thickness for the diagnosis of FPLD. A combination of gluteal fat thickness ≤13 mm and pubic/gluteal fat ratio ≥2.5 (based on a receiver operating characteristic curve) provided 96.67% (95% CI, 82.78-99.92) sensitivity and 91.38% (95% CI, 81.02-97.14) specificity in the overall cohort and 100.00% (95% CI, 87.23-100.00) sensitivity and 90.00% (95% CI, 76.34-97.21) specificity in females for the diagnosis of FPLD. When this approach was tested in a larger dataset of random patients, FPLD was differentiated from subjects without lipodystrophy with 96.67% (95% CI, 82.78-99.92) sensitivity and 100.00% (95% CI, 98.73-100.00) specificity. When only women were analyzed, the sensitivity and the specificity was 100.00% (95% CI, 87.23-100.00 and 97.95-100.00, respectively). The performance of gluteal fat thickness and pubic/gluteal fat thickness ratio was comparable to readouts performed by radiologists with expertise in lipodystrophy. Conclusion The combined use of gluteal fat thickness and pubic/gluteal fat ratio from pelvic MRI is a promising method to diagnose FPLD that can reliably identify FPLD in women. Our findings need to be tested in larger populations and prospectively.

Funder

Aegerion Pharmaceuticals

Amryt Pharmaceuticals

Regeneron Pharmaceuticals

Third Rock Ventures

Amryt

AstraZeneca

Lilly

MSD

Novartis

Novo Nordisk

Boehringer-Ingelheim

Servier

Sanofi-Aventis

Ionis Pharmaceuticals

Akcea Therapeutics

Gemphire Therapeutics

GI Dynamics

Thera Therapeutics

BMS

Rhythm Pharmaceuticals

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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