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Reduced gut microbiota diversity in patients with congenital generalized lipodystrophy

BACKGROUND: Previous studies suggest intestinal dysbiosis is associated with metabolic diseases. However, the causal relationship between them is not fully elucidated. Gut microbiota evaluation of patients with congenital generalized lipodystrophy (CGL), a disease characterized by the absence of sub...

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Detalles Bibliográficos
Autores principales: Montenegro Junior, Renan Magalhães, Ponte, Clarisse Mourão Melo, Castelo, Maria Helane Costa Gurgel, de Oliveira Silveira, Alessandro Conrado, Fernandes, Virgínia Oliveira, D’Alva, Catarina Brasil, Oliveira, Luiz Felipe Valter, Hristov, Angélica Domingues, Bandeira, Silviane Praciano, da Cruz Paiva, Grayce Ellen, Levi, José Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9508722/
https://www.ncbi.nlm.nih.gov/pubmed/36153588
http://dx.doi.org/10.1186/s13098-022-00908-8
Descripción
Sumario:BACKGROUND: Previous studies suggest intestinal dysbiosis is associated with metabolic diseases. However, the causal relationship between them is not fully elucidated. Gut microbiota evaluation of patients with congenital generalized lipodystrophy (CGL), a disease characterized by the absence of subcutaneous adipose tissue, insulin resistance, and diabetes since the first years of life, could provide insights into these relationships. METHODS: A cross-sectional study was conducted with patients with CGL (n = 17) and healthy individuals (n = 17). The gut microbiome study was performed by sequencing the 16S rRNA gene through High-Throughput Sequencing (BiomeHub Biotechnologies, Brazil). RESULTS: The median age was 20.0 years old, and 64.7% were female. There was no difference between groups in pubertal stage, BMI, ethnicity, origin (rural or urban), delivery, breastfeeding, caloric intake, macronutrient, or fiber consumption. Lipodystrophic patients presented a lower alpha diversity (Richness index: 54.0 versus 67.5; p = 0.008). No differences were observed in the diversity parameters when analyzing the presence of diabetes, its complications, or the CGL subtype. CONCLUSION: In this study, we demonstrate for the first time a reduced gut microbiota diversity in individuals with CGL. Dysbiosis was present despite dietary treatment and was also observed in young patients. Our findings allow us to speculate that the loss of intestinal microbiota diversity may be due to metabolic abnormalities present since the first years of life in CGL. Longitudinal studies are needed to confirm these findings, clarifying the possible causal link between dysbiosis and insulin resistance in humans. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-022-00908-8.