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Aim: Observational studies have suggested an association between celiac disease and thyroid dysfunction, but their causal relationship has not yet been established.
Methods: Summary statistics for celiac disease were retrieved from the FinnGen Consortium, thyroid hormone and antibody data were obtained from the ThyroidOmics Consortium, and genetic variants associated with hyperthyroidism and hypothyroidism were sourced from the UK Biobank. MR statistical analyses used the inverse variance weighted algorithm, followed by various sensitivity analyses and reliability evaluations.
Results: Genetic proxied celiac disease was significantly associated with increased free thyroxine (FT4) and thyroid peroxidase antibody (TPOAb) levels and decreased free triiodothyronine (FT3)/FT4 ratio, whereas the causality of this common enteropathy on thyroid stimulating hormone (TSH), FT3, total triiodothyronine (TT3), and TT3/FT4 ratio (and vice versa) is unfounded. Moreover, the findings of MR analysis tend to favor the causality of celiac disease for hyperthyroidism, but not hypothyroidism.
Conclusion: By leveraging large GWAS consortia datasets, our MR study indicates that the genetic liability to celiac disease is suggestively detrimental to the homeostasis of FT4 and TPOAb levels and FT3/FT4 ratio. Our findings provide caution regarding the risk of hyperthyroidism but not hypothyroidism for individuals suffering from celiac disease.
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http://dx.doi.org/10.2174/0118715303364014250713045734 | DOI Listing |
Genes Immun
September 2025
Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
In coeliac disease (CeD), the epithelial lining (EL) of the small intestine is severely damaged by a complex auto-inflammatory response, leading intraepithelial lymphocytes to attack epithelial cells. To understand the intestinal changes and genetic regulation in CeD, we investigated the heterogeneity in the transcriptomic profile of the duodenal EL using RNA-seq and eQTL analysis on predicted cell types. The study included duodenal biopsies from 82 patients, grouped into controls, gluten-free diet treated CeD and untreated CeD.
View Article and Find Full Text PDFAnn Afr Med
September 2025
Department of Medical Gastroenterology, JSS Medical College and Hospital, JSS AHER, Mysore, Karnataka, India.
Aims: The aim is to assess the usefulness of routine duodenal biopsy in patients presenting with iron deficiency anemia in areas with low prevalence of celiac disease (CD).
Methods: This prospective study included 156 patients with unexplained iron deficiency anemia, referred to the Department of Gastroenterology. JSS Medical College and Hospital, Mysuru, India.
Clin Exp Immunol
September 2025
Mucosal Immunology Lab, Department of Paediatrics and Immunology. Universidad de Valladolid. Valladolid. Spain.
Introduction: Although Coeliac disease (CD) current and only treatment is a life-long strict gluten free diet (GFD), some patients suffer from persistent duodenal lesions despite years into the diet. Hence, we aimed to study the effect that the GFD elicits on the mucosal immune infiltrate from these patients.
Method: To that end, duodenal biopsies were collected from non-coeliac controls and CD patients, both at diagnosis and after at least one year into the GFD.
JTCVS Open
August 2025
State Key Laboratory of Cardiovascular Disease, Center of Vascular Surgery, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Objective: To evaluate the remodeling of the distal aorta and outcomes after aortic surgery for type A aortic dissection (TAAD) in patients with Marfan syndrome and investigate whether morphologic characteristics of the dissection can predict negative remodeling.
Methods: Between 2013 and 2021, we performed total arch with a frozen elephant trunk for 325 patients with Marfan syndrome with DeBakey type I aortic dissection. Mean age was 47.
Oman Med J
March 2025
Freelance Public Health Senior Consultant, Muscat, Oman.
Objectives: Selective immunoglobulin A deficiency (SIgAD) is characterized by an isolated deficiency of serum IgA while immunoglobulin G (IgG) and immunoglobulin M (IgM) levels remain normal. Symptoms range from asymptomatic to recurrent infections. We aimed to determine the prevalence of IgAD and SIgAD among Omani patients undergoing screening for celiac disease.
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