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Refining Evaluation of Bone Mass and Adipose Distribution in Dunnigan Syndrome

Familial partial lipodystrophies (FPLD) are rare diseases characterized by selective loss of subcutaneous adipose tissue at different sites. This cross-sectional observational study aimed to estimate adipose tissue in the bone marrow (BMAT), intra (IMCL) and extra-myocyte lipids (EMCL), and define t...

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Autores principales: Moreira, Mariana Lima Mascarenhas, de Araújo, Iana Mizumukai, Fukada, Sandra Yasuyo, Venturini, Lucas Gabriel R., Guidorizzi, Natalia Rossin, Garrido, Carlos Ernesto, Rosen, Clifford J., de Paula, Francisco José Albuquerque
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488191/
https://www.ncbi.nlm.nih.gov/pubmed/37685926
http://dx.doi.org/10.3390/ijms241713118
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author Moreira, Mariana Lima Mascarenhas
de Araújo, Iana Mizumukai
Fukada, Sandra Yasuyo
Venturini, Lucas Gabriel R.
Guidorizzi, Natalia Rossin
Garrido, Carlos Ernesto
Rosen, Clifford J.
de Paula, Francisco José Albuquerque
author_facet Moreira, Mariana Lima Mascarenhas
de Araújo, Iana Mizumukai
Fukada, Sandra Yasuyo
Venturini, Lucas Gabriel R.
Guidorizzi, Natalia Rossin
Garrido, Carlos Ernesto
Rosen, Clifford J.
de Paula, Francisco José Albuquerque
author_sort Moreira, Mariana Lima Mascarenhas
collection PubMed
description Familial partial lipodystrophies (FPLD) are rare diseases characterized by selective loss of subcutaneous adipose tissue at different sites. This cross-sectional observational study aimed to estimate adipose tissue in the bone marrow (BMAT), intra (IMCL) and extra-myocyte lipids (EMCL), and define the bone phenotype in the context of FPLD2/Dunnigan syndrome (DS). The subjects comprised 23 controls (C) and 18 DS patients, matched by age, weight and height. Blood samples, dual-energy X-ray absorptiometry for bone mineral density (BMD) and trabecular bone score (TBS) and 1H-spectroscopy using magnetic resonance to estimate BMAT in the lumbar spine, IMCL, EMCL and osteoclastogenesis were assessed. The prevalence of diabetes mellitus was 78% in DS patients. Glucose, HbA1c, triglycerides, insulin and HOMA-IR levels were elevated in DS, whereas HDLc, 25(OH)D, PTH and osteocalcin levels were reduced. BMD was similar between groups at all sites, except 1/3 radius, which was lower in DS group. TBS was reduced in DS. DS presented increased osteoclastogenesis and elevated BMAT, with greater saturation levels and higher IMCL than the C group. HOMA-IR and EMCL were negatively associated with TBS; osteocalcin and EMCL were correlated negatively with BMD. This study contributes to refining the estimation of adipose tissue in DS by showing increased adiposity in the lumbar spine and muscle tissue. DXA detected lower TBS and BMD in the 1/3 radius, suggesting impairment in bone quality and that bone mass is mainly affected in the cortical bone.
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spelling pubmed-104881912023-09-09 Refining Evaluation of Bone Mass and Adipose Distribution in Dunnigan Syndrome Moreira, Mariana Lima Mascarenhas de Araújo, Iana Mizumukai Fukada, Sandra Yasuyo Venturini, Lucas Gabriel R. Guidorizzi, Natalia Rossin Garrido, Carlos Ernesto Rosen, Clifford J. de Paula, Francisco José Albuquerque Int J Mol Sci Article Familial partial lipodystrophies (FPLD) are rare diseases characterized by selective loss of subcutaneous adipose tissue at different sites. This cross-sectional observational study aimed to estimate adipose tissue in the bone marrow (BMAT), intra (IMCL) and extra-myocyte lipids (EMCL), and define the bone phenotype in the context of FPLD2/Dunnigan syndrome (DS). The subjects comprised 23 controls (C) and 18 DS patients, matched by age, weight and height. Blood samples, dual-energy X-ray absorptiometry for bone mineral density (BMD) and trabecular bone score (TBS) and 1H-spectroscopy using magnetic resonance to estimate BMAT in the lumbar spine, IMCL, EMCL and osteoclastogenesis were assessed. The prevalence of diabetes mellitus was 78% in DS patients. Glucose, HbA1c, triglycerides, insulin and HOMA-IR levels were elevated in DS, whereas HDLc, 25(OH)D, PTH and osteocalcin levels were reduced. BMD was similar between groups at all sites, except 1/3 radius, which was lower in DS group. TBS was reduced in DS. DS presented increased osteoclastogenesis and elevated BMAT, with greater saturation levels and higher IMCL than the C group. HOMA-IR and EMCL were negatively associated with TBS; osteocalcin and EMCL were correlated negatively with BMD. This study contributes to refining the estimation of adipose tissue in DS by showing increased adiposity in the lumbar spine and muscle tissue. DXA detected lower TBS and BMD in the 1/3 radius, suggesting impairment in bone quality and that bone mass is mainly affected in the cortical bone. MDPI 2023-08-23 /pmc/articles/PMC10488191/ /pubmed/37685926 http://dx.doi.org/10.3390/ijms241713118 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Moreira, Mariana Lima Mascarenhas
de Araújo, Iana Mizumukai
Fukada, Sandra Yasuyo
Venturini, Lucas Gabriel R.
Guidorizzi, Natalia Rossin
Garrido, Carlos Ernesto
Rosen, Clifford J.
de Paula, Francisco José Albuquerque
Refining Evaluation of Bone Mass and Adipose Distribution in Dunnigan Syndrome
title Refining Evaluation of Bone Mass and Adipose Distribution in Dunnigan Syndrome
title_full Refining Evaluation of Bone Mass and Adipose Distribution in Dunnigan Syndrome
title_fullStr Refining Evaluation of Bone Mass and Adipose Distribution in Dunnigan Syndrome
title_full_unstemmed Refining Evaluation of Bone Mass and Adipose Distribution in Dunnigan Syndrome
title_short Refining Evaluation of Bone Mass and Adipose Distribution in Dunnigan Syndrome
title_sort refining evaluation of bone mass and adipose distribution in dunnigan syndrome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10488191/
https://www.ncbi.nlm.nih.gov/pubmed/37685926
http://dx.doi.org/10.3390/ijms241713118
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