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Association of vitamin D and functional dyspepsia: a case-control study

BACKGROUND: Vitamin D plays a key role in responses of brain-gut axis. It has been suggested that functional dyspepsia (FD) may be associated with decreased levels of vitamin D. Hence this study wished to find the association between vitamin D in patients with FD. MATERIALS AND METHODS: This case-co...

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Autores principales: Das, Dhriti Sundar, Saharia, Gautom Kumar, Panigrahi, Manas Kumar, Sahoo, Debananda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553082/
https://www.ncbi.nlm.nih.gov/pubmed/37811112
http://dx.doi.org/10.1097/MS9.0000000000001204
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author Das, Dhriti Sundar
Saharia, Gautom Kumar
Panigrahi, Manas Kumar
Sahoo, Debananda
author_facet Das, Dhriti Sundar
Saharia, Gautom Kumar
Panigrahi, Manas Kumar
Sahoo, Debananda
author_sort Das, Dhriti Sundar
collection PubMed
description BACKGROUND: Vitamin D plays a key role in responses of brain-gut axis. It has been suggested that functional dyspepsia (FD) may be associated with decreased levels of vitamin D. Hence this study wished to find the association between vitamin D in patients with FD. MATERIALS AND METHODS: This case-control study was done at a tertiary care hospital with 150 cases and 150 controls. FD was diagnosed by the ROME IV criteria. Demographic profile and serum vitamin D levels including Perceived Stress Score (PSS) and salivary amylase were determined for both cases and controls. RESULTS: Majority of the FD cases were males (57.3%). Post-prandial distress syndrome represented the major type of FD cases (69.3%). A higher mean BMI was found among the control group (23.2 vs. 21.2, P<0.05) and higher percentage of obese individuals in the control group (42.7% vs. 29.3%, P= 0.05). Majority of the cases are from rural background (89.3% vs. 74%, P<0.001). Comparison of PSS showed that cases had significantly higher grades of PSS than control (P<0.001). However, no significant association was found in the levels of salivary amylase between the groups (P=0.728). Hypovitaminosis D (<30 ng/ml) was found significantly more among cases than controls (73.3% vs. 60%; P<0.05) with an odds ratio of 1.833 (CI 95%= 1.126–2.985). After adjustment of age, place of residence and BMI, vitamin D levels were significantly associated with FD in the regression analysis. CONCLUSION: This study shows significant association of vitamin D deficiency in FD patients. It also opens up new avenues for further research into the role of vitamin D supplementation to further improve the management of such cases.
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spelling pubmed-105530822023-10-06 Association of vitamin D and functional dyspepsia: a case-control study Das, Dhriti Sundar Saharia, Gautom Kumar Panigrahi, Manas Kumar Sahoo, Debananda Ann Med Surg (Lond) Original Research BACKGROUND: Vitamin D plays a key role in responses of brain-gut axis. It has been suggested that functional dyspepsia (FD) may be associated with decreased levels of vitamin D. Hence this study wished to find the association between vitamin D in patients with FD. MATERIALS AND METHODS: This case-control study was done at a tertiary care hospital with 150 cases and 150 controls. FD was diagnosed by the ROME IV criteria. Demographic profile and serum vitamin D levels including Perceived Stress Score (PSS) and salivary amylase were determined for both cases and controls. RESULTS: Majority of the FD cases were males (57.3%). Post-prandial distress syndrome represented the major type of FD cases (69.3%). A higher mean BMI was found among the control group (23.2 vs. 21.2, P<0.05) and higher percentage of obese individuals in the control group (42.7% vs. 29.3%, P= 0.05). Majority of the cases are from rural background (89.3% vs. 74%, P<0.001). Comparison of PSS showed that cases had significantly higher grades of PSS than control (P<0.001). However, no significant association was found in the levels of salivary amylase between the groups (P=0.728). Hypovitaminosis D (<30 ng/ml) was found significantly more among cases than controls (73.3% vs. 60%; P<0.05) with an odds ratio of 1.833 (CI 95%= 1.126–2.985). After adjustment of age, place of residence and BMI, vitamin D levels were significantly associated with FD in the regression analysis. CONCLUSION: This study shows significant association of vitamin D deficiency in FD patients. It also opens up new avenues for further research into the role of vitamin D supplementation to further improve the management of such cases. Lippincott Williams & Wilkins 2023-08-16 /pmc/articles/PMC10553082/ /pubmed/37811112 http://dx.doi.org/10.1097/MS9.0000000000001204 Text en Copyright © 2023 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Research
Das, Dhriti Sundar
Saharia, Gautom Kumar
Panigrahi, Manas Kumar
Sahoo, Debananda
Association of vitamin D and functional dyspepsia: a case-control study
title Association of vitamin D and functional dyspepsia: a case-control study
title_full Association of vitamin D and functional dyspepsia: a case-control study
title_fullStr Association of vitamin D and functional dyspepsia: a case-control study
title_full_unstemmed Association of vitamin D and functional dyspepsia: a case-control study
title_short Association of vitamin D and functional dyspepsia: a case-control study
title_sort association of vitamin d and functional dyspepsia: a case-control study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553082/
https://www.ncbi.nlm.nih.gov/pubmed/37811112
http://dx.doi.org/10.1097/MS9.0000000000001204
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