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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Montenegro Junior, Renan Magalhães |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-9508722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95087222022-09-25 Reduced gut microbiota diversity in patients with congenital generalized lipodystrophy 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 Diabetol Metab Syndr Research 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. BioMed Central 2022-09-24 /pmc/articles/PMC9508722/ /pubmed/36153588 http://dx.doi.org/10.1186/s13098-022-00908-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research 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 Reduced gut microbiota diversity in patients with congenital generalized lipodystrophy |
title | Reduced gut microbiota diversity in patients with congenital generalized lipodystrophy |
title_full | Reduced gut microbiota diversity in patients with congenital generalized lipodystrophy |
title_fullStr | Reduced gut microbiota diversity in patients with congenital generalized lipodystrophy |
title_full_unstemmed | Reduced gut microbiota diversity in patients with congenital generalized lipodystrophy |
title_short | Reduced gut microbiota diversity in patients with congenital generalized lipodystrophy |
title_sort | reduced gut microbiota diversity in patients with congenital generalized lipodystrophy |
topic | Research |
url | 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 |
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