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Insomnia and risk of nonalcoholic fatty liver disease: A systematic review and meta-analysis
AIM: This sudy aims to investigate the association between insomnia or excessive daytime sleepiness (EDS) and risk of nonalcoholic fatty liver disease (NAFLD). METHODS: We searched published studies indexed in MEDLINE and EMBASE database from inception to December 2015. Studies that reported odds ra...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664866/ https://www.ncbi.nlm.nih.gov/pubmed/28862239 http://dx.doi.org/10.4103/jpgm.JPGM_140_17 |
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author | Wijarnpreecha, K Thongprayoon, C Panjawatanan, P Ungprasert, P |
author_facet | Wijarnpreecha, K Thongprayoon, C Panjawatanan, P Ungprasert, P |
author_sort | Wijarnpreecha, K |
collection | PubMed |
description | AIM: This sudy aims to investigate the association between insomnia or excessive daytime sleepiness (EDS) and risk of nonalcoholic fatty liver disease (NAFLD). METHODS: We searched published studies indexed in MEDLINE and EMBASE database from inception to December 2015. Studies that reported odds ratios (ORs), risk ratios, hazard ratios or standardized incidence ratio with 95% confidence intervals (CI) comparing the risk of NAFLD among participants who had insomnia or EDS versus those without insomnia or EDS were included. Pooled ORs and 95% CI were calculated using a random-effect, generic inverse variance method of DerSimonian and Laird. Cochran's Q test and I(2) statistic were used to determine the between-study heterogeneity. RESULTS: Our search strategy yielded 2117 potentially relevant articles (781 articles from MEDLINE and 1336 articles from EMBASE). After comprehensive review, seven studies (three cross-sectional studies and four case–control studies) were found to be eligible and were included in the meta-analysis. The risk of NAFLD in participants who had insomnia was significantly higher with the pooled OR of 1.13 (95% CI, 1.00–1.27). The statistical heterogeneity was moderate with an I(2) of 62%. Elevated risk of NAFLD was also observed among participants with EDS even though the 95% CI was wider and did not reach statistical significance (pooled OR 2.21; 95% CI, 0.84–5.82). The statistical heterogeneity was moderate with an I(2) of 62%. CONCLUSIONS: Our study demonstrated an increased risk of NAFLD among participants who had insomnia or EDS. Whether this association is causal needs further investigations. |
format | Online Article Text |
id | pubmed-5664866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56648662017-12-26 Insomnia and risk of nonalcoholic fatty liver disease: A systematic review and meta-analysis Wijarnpreecha, K Thongprayoon, C Panjawatanan, P Ungprasert, P J Postgrad Med Original Article AIM: This sudy aims to investigate the association between insomnia or excessive daytime sleepiness (EDS) and risk of nonalcoholic fatty liver disease (NAFLD). METHODS: We searched published studies indexed in MEDLINE and EMBASE database from inception to December 2015. Studies that reported odds ratios (ORs), risk ratios, hazard ratios or standardized incidence ratio with 95% confidence intervals (CI) comparing the risk of NAFLD among participants who had insomnia or EDS versus those without insomnia or EDS were included. Pooled ORs and 95% CI were calculated using a random-effect, generic inverse variance method of DerSimonian and Laird. Cochran's Q test and I(2) statistic were used to determine the between-study heterogeneity. RESULTS: Our search strategy yielded 2117 potentially relevant articles (781 articles from MEDLINE and 1336 articles from EMBASE). After comprehensive review, seven studies (three cross-sectional studies and four case–control studies) were found to be eligible and were included in the meta-analysis. The risk of NAFLD in participants who had insomnia was significantly higher with the pooled OR of 1.13 (95% CI, 1.00–1.27). The statistical heterogeneity was moderate with an I(2) of 62%. Elevated risk of NAFLD was also observed among participants with EDS even though the 95% CI was wider and did not reach statistical significance (pooled OR 2.21; 95% CI, 0.84–5.82). The statistical heterogeneity was moderate with an I(2) of 62%. CONCLUSIONS: Our study demonstrated an increased risk of NAFLD among participants who had insomnia or EDS. Whether this association is causal needs further investigations. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5664866/ /pubmed/28862239 http://dx.doi.org/10.4103/jpgm.JPGM_140_17 Text en Copyright: © 2017 Journal of Postgraduate Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Wijarnpreecha, K Thongprayoon, C Panjawatanan, P Ungprasert, P Insomnia and risk of nonalcoholic fatty liver disease: A systematic review and meta-analysis |
title | Insomnia and risk of nonalcoholic fatty liver disease: A systematic review and meta-analysis |
title_full | Insomnia and risk of nonalcoholic fatty liver disease: A systematic review and meta-analysis |
title_fullStr | Insomnia and risk of nonalcoholic fatty liver disease: A systematic review and meta-analysis |
title_full_unstemmed | Insomnia and risk of nonalcoholic fatty liver disease: A systematic review and meta-analysis |
title_short | Insomnia and risk of nonalcoholic fatty liver disease: A systematic review and meta-analysis |
title_sort | insomnia and risk of nonalcoholic fatty liver disease: a systematic review and meta-analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664866/ https://www.ncbi.nlm.nih.gov/pubmed/28862239 http://dx.doi.org/10.4103/jpgm.JPGM_140_17 |
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