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Anthropometric measurements as a key diagnostic tool for familial partial lipodystrophy in women.
Veras, Victor Rezende; da Cruz Paiva Lima, Grayce Ellen; da Ponte Melo, Ivana; Fernandes, Virginia Oliveira; de Moura Lopes, Fabia Karine; do Amaral, Camila Lopes; Castelo, Maria Helane Gurgel; Queiroz, Larissa Luna; Araújo, Jessica Silveira; Valerio, Cynthia Melissa; Montenegro Junior, Renan Magalhães.
Afiliação
  • Veras VR; Brazilian Group for the Study of Inherited and Acquired Lipodystrophies (BRAZLIPO), Fortaleza, CE, Brazil.
  • da Cruz Paiva Lima GE; Clinical Research Unit, Walter Cantídio University Hospital, Federal University of Ceará/EBSERH, Fortaleza, CE, Brazil.
  • da Ponte Melo I; Department of Clinical Medicine, Federal University of Ceará, Fortaleza, CE, Brazil.
  • Fernandes VO; Brazilian Group for the Study of Inherited and Acquired Lipodystrophies (BRAZLIPO), Fortaleza, CE, Brazil.
  • de Moura Lopes FK; University of Fortaleza, (UNIFOR), Fortaleza, CE, Brazil.
  • do Amaral CL; Diagnosticos das Americas DASA, São Paulo, Brazil.
  • Castelo MHG; Brazilian Group for the Study of Inherited and Acquired Lipodystrophies (BRAZLIPO), Fortaleza, CE, Brazil.
  • Queiroz LL; Clinical Research Unit, Walter Cantídio University Hospital, Federal University of Ceará/EBSERH, Fortaleza, CE, Brazil.
  • Araújo JS; Department of Clinical Medicine, Federal University of Ceará, Fortaleza, CE, Brazil.
  • Valerio CM; Brazilian Group for the Study of Inherited and Acquired Lipodystrophies (BRAZLIPO), Fortaleza, CE, Brazil.
  • Montenegro Junior RM; Clinical Research Unit, Walter Cantídio University Hospital, Federal University of Ceará/EBSERH, Fortaleza, CE, Brazil.
Diabetol Metab Syndr ; 16(1): 216, 2024 Sep 04.
Article em En | MEDLINE | ID: mdl-39227868
ABSTRACT

BACKGROUND:

Familial Partial Lipodystrophy (FPLD) is a disease with wide clinical and genetic variation, with seven different subtypes described. Until genetic testing becomes feasible in clinical practice, non-invasive tools are used to evaluate body composition in lipodystrophic patients. This study aimed to analyze the different anthropometric parameters used for screening and diagnosis of FPLD, such as thigh skinfold thickness (TS), Köb index (Köbi), leg fat percentage (LFP), fat mass ratio (FMR) and leg-to-total fat mass ratio in grams (LTR), by dual-energy X-ray absorptiometry, focusing on determining cutoff points for TS and LFP within a Brazilian population.

METHODS:

Thirty-seven patients with FPLD and seventy-four healthy controls matched for body mass index, sex and age were studied. Data were collected through medical record review after signing informed consent. All participants had body fat distribution evaluated by skinfolds and DXA measures. Fasting blood samples were collected to evaluate glycemic and lipid profiles. Genetic studies were carried out on all patients. Two groups were categorized based on genetic testing and/or anthropometric characteristics FPLD+ (positive genetic test) and FPLD1 (negative genetic testing, but positive clinical/anthropometric criteria for FPLD).

RESULTS:

Eighteen (48.6%) patients were classified as FPLD+, and 19 (51.4%) as FPLD1. Unlike what is described in the literature, the LMNA variant in codon 582 was the most common. Among the main diagnostic parameters of FPLD, a statistical difference was observed between the groups for, Köbi, TS, LFP, FMR, and LTR. A cutoff point of 20 mm for TS in FPLD women was found, which is lower than the value classically described in the literature for the diagnosis of FPLD. Additionally, an LFP < 29.6% appears to be a useful tool to aid in the diagnosis of these women.

CONCLUSION:

Combining anthropometric measurements to assess body fat distribution can lead to a more accurate diagnosis of FPLD. This study suggests new cutoff points for thigh skinfold and leg fat percentage in women with suspected FPLD in Brazil. Further studies are needed to confirm these findings.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Diabetol Metab Syndr Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Diabetol Metab Syndr Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Reino Unido