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Are Patients with Axial Spondyloarthritis Who Were Breastfed Protected against the Development of Severe Disease?

Background and aims: Breastfeeding is recognized as one of the most influential drivers of the gut microbiome. In turn, alterations in the gut microbiome may play a role in the development and severity of spondyloarthritis (SpA). We aimed to analyze different disease outcomes in patients with axial...

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Autores principales: Alonso, Sara, Braña, Ignacio, Pardo, Estefanía, Burger, Stefanie, González del Pozo, Pablo, Alperi, Mercedes, Queiro, Rubén
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003909/
https://www.ncbi.nlm.nih.gov/pubmed/36902650
http://dx.doi.org/10.3390/jcm12051863
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author Alonso, Sara
Braña, Ignacio
Pardo, Estefanía
Burger, Stefanie
González del Pozo, Pablo
Alperi, Mercedes
Queiro, Rubén
author_facet Alonso, Sara
Braña, Ignacio
Pardo, Estefanía
Burger, Stefanie
González del Pozo, Pablo
Alperi, Mercedes
Queiro, Rubén
author_sort Alonso, Sara
collection PubMed
description Background and aims: Breastfeeding is recognized as one of the most influential drivers of the gut microbiome. In turn, alterations in the gut microbiome may play a role in the development and severity of spondyloarthritis (SpA). We aimed to analyze different disease outcomes in patients with axial SpA (axSpA) based on the history of breastfeeding. Patients and methods: A random sample was selected from a large database of axSpA patients. Patients were divided based on history of breastfeeding and several disease outcomes were compared. Both groups were also compared based on disease severity. Adjusted linear and logistic regression statistical methods were used. Results: The study included 105 patients (46 women and 59 men), and the median age was 45 years (IQR: 16–72), and the mean age at diagnosis was 34.3 ± 10.9 years. Sixty-one patients (58.1%) were breastfed, with a median duration of 4 (IQR: 1–24) months. After the fully adjusted model, BASDAI [−1.13 (95%CI: −2.04, −0.23), p = 0.015] and ASDAS [−0.38 (95%CI: −0.72, −0.04), p = 0.030] scores were significantly lower in breastfed patients. Forty-two percent had severe disease. In the adjusted logistic model for age, sex, disease duration, family history, HLA-B27, biologic therapy, smoking, and obesity, breastfeeding had a protective effect against the development of severe disease (OR 0.22, 95%CI: 0.08–0.57, p = 0.003). The selected sample size was sufficient to detect this difference with a statistical power of 87% and a confidence level of 95%. Conclusion: Breastfeeding might exert a protective effect against severe disease in patients with axSpA. These data need further confirmation.
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spelling pubmed-100039092023-03-11 Are Patients with Axial Spondyloarthritis Who Were Breastfed Protected against the Development of Severe Disease? Alonso, Sara Braña, Ignacio Pardo, Estefanía Burger, Stefanie González del Pozo, Pablo Alperi, Mercedes Queiro, Rubén J Clin Med Article Background and aims: Breastfeeding is recognized as one of the most influential drivers of the gut microbiome. In turn, alterations in the gut microbiome may play a role in the development and severity of spondyloarthritis (SpA). We aimed to analyze different disease outcomes in patients with axial SpA (axSpA) based on the history of breastfeeding. Patients and methods: A random sample was selected from a large database of axSpA patients. Patients were divided based on history of breastfeeding and several disease outcomes were compared. Both groups were also compared based on disease severity. Adjusted linear and logistic regression statistical methods were used. Results: The study included 105 patients (46 women and 59 men), and the median age was 45 years (IQR: 16–72), and the mean age at diagnosis was 34.3 ± 10.9 years. Sixty-one patients (58.1%) were breastfed, with a median duration of 4 (IQR: 1–24) months. After the fully adjusted model, BASDAI [−1.13 (95%CI: −2.04, −0.23), p = 0.015] and ASDAS [−0.38 (95%CI: −0.72, −0.04), p = 0.030] scores were significantly lower in breastfed patients. Forty-two percent had severe disease. In the adjusted logistic model for age, sex, disease duration, family history, HLA-B27, biologic therapy, smoking, and obesity, breastfeeding had a protective effect against the development of severe disease (OR 0.22, 95%CI: 0.08–0.57, p = 0.003). The selected sample size was sufficient to detect this difference with a statistical power of 87% and a confidence level of 95%. Conclusion: Breastfeeding might exert a protective effect against severe disease in patients with axSpA. These data need further confirmation. MDPI 2023-02-27 /pmc/articles/PMC10003909/ /pubmed/36902650 http://dx.doi.org/10.3390/jcm12051863 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
Alonso, Sara
Braña, Ignacio
Pardo, Estefanía
Burger, Stefanie
González del Pozo, Pablo
Alperi, Mercedes
Queiro, Rubén
Are Patients with Axial Spondyloarthritis Who Were Breastfed Protected against the Development of Severe Disease?
title Are Patients with Axial Spondyloarthritis Who Were Breastfed Protected against the Development of Severe Disease?
title_full Are Patients with Axial Spondyloarthritis Who Were Breastfed Protected against the Development of Severe Disease?
title_fullStr Are Patients with Axial Spondyloarthritis Who Were Breastfed Protected against the Development of Severe Disease?
title_full_unstemmed Are Patients with Axial Spondyloarthritis Who Were Breastfed Protected against the Development of Severe Disease?
title_short Are Patients with Axial Spondyloarthritis Who Were Breastfed Protected against the Development of Severe Disease?
title_sort are patients with axial spondyloarthritis who were breastfed protected against the development of severe disease?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10003909/
https://www.ncbi.nlm.nih.gov/pubmed/36902650
http://dx.doi.org/10.3390/jcm12051863
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