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Serum HBV surface antigen positivity is associated with low prevalence of metabolic syndrome: A meta-analysis
As there is conflicting evidence for the relationship between hepatitis B virus surface antigen (HBsAg) positivity and the prevalence of metabolic syndrome (MetS), we performed a meta-analysis to investigate whether HBsAg positivity affects the incidence of MetS. Observational studies on the relatio...
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Published in: | PloS one 2017-05, Vol.12 (5), p.e0177713-e0177713 |
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description | As there is conflicting evidence for the relationship between hepatitis B virus surface antigen (HBsAg) positivity and the prevalence of metabolic syndrome (MetS), we performed a meta-analysis to investigate whether HBsAg positivity affects the incidence of MetS.
Observational studies on the relationship between HBsAg positivity and MetS were obtained from PubMed, Web of Science, and the Cochrane Library in April 2016. The pooled odds ratios (ORs) of MetS and its components (central obesity, increased fasting glucose, increased blood pressure, dyslipidemia) for subjects with or without HBsAg positivity were synthesized. The standardized mean difference of MetS components between HBsAg-positive participants and healthy controls was calculated. Heterogeneity was explored with subgroup analysis and sensitivity analysis. Publication bias was detected using Egger's test and Begg's test.
Thirty studies were eligible for meta-analysis. The MetS OR for HBsAg-positive participants was significantly decreased compared with the controls [OR = 0.80, 95% confidence interval (CI), 0.70-0.90]. The negative effect of HBsAg positivity on elevated triglycerides (OR = 0.62, 95% CI, 0.59-0.64) was strong, while that for increased fasting blood glucose was weak (OR = 0.94, 95% CI, 0.90-0.98). The pooled ORs of central obesity (OR = 0.97, 95% CI, 0.91-1.04), reduced high-density lipoprotein cholesterol (OR = 0.98, 95% CI, 0.83-1.14), and elevated blood pressure (OR = 1.00, 95% CI, 0.80-1.25) for HBsAg-positive participants were all not significantly different compared with the controls. No publication bias was detected.
Serum HBsAg positivity is inversely associated with the prevalence of MetS. Among the five components of MetS, elevated triglycerides had the strongest inverse relationship with HBsAg positivity. |
doi_str_mv | 10.1371/journal.pone.0177713 |
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Observational studies on the relationship between HBsAg positivity and MetS were obtained from PubMed, Web of Science, and the Cochrane Library in April 2016. The pooled odds ratios (ORs) of MetS and its components (central obesity, increased fasting glucose, increased blood pressure, dyslipidemia) for subjects with or without HBsAg positivity were synthesized. The standardized mean difference of MetS components between HBsAg-positive participants and healthy controls was calculated. Heterogeneity was explored with subgroup analysis and sensitivity analysis. Publication bias was detected using Egger's test and Begg's test.
Thirty studies were eligible for meta-analysis. The MetS OR for HBsAg-positive participants was significantly decreased compared with the controls [OR = 0.80, 95% confidence interval (CI), 0.70-0.90]. The negative effect of HBsAg positivity on elevated triglycerides (OR = 0.62, 95% CI, 0.59-0.64) was strong, while that for increased fasting blood glucose was weak (OR = 0.94, 95% CI, 0.90-0.98). The pooled ORs of central obesity (OR = 0.97, 95% CI, 0.91-1.04), reduced high-density lipoprotein cholesterol (OR = 0.98, 95% CI, 0.83-1.14), and elevated blood pressure (OR = 1.00, 95% CI, 0.80-1.25) for HBsAg-positive participants were all not significantly different compared with the controls. No publication bias was detected.
Serum HBsAg positivity is inversely associated with the prevalence of MetS. Among the five components of MetS, elevated triglycerides had the strongest inverse relationship with HBsAg positivity.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0177713</identifier><identifier>PMID: 28505202</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adiponectin ; Age composition ; Analysis ; Antigens ; Antiviral agents ; Arteriosclerosis ; Atherosclerosis ; Bias ; Biology and Life Sciences ; Biomarkers ; Blood ; Blood pressure ; Body mass ; Body mass index ; Cardiovascular diseases ; Cholesterol ; Chronic active hepatitis ; Chronic infection ; Cirrhosis ; Diabetes ; Diabetes mellitus ; Disease resistance ; Dyslipidemia ; Fasting ; Glucose ; Glucose metabolism ; Heart diseases ; Hepatitis ; Hepatitis B surface antigen ; Hepatitis B Surface Antigens - blood ; Heterogeneity ; Hospitals ; Humans ; Hypertension ; Incidence ; Infections ; Influence ; Insulin ; Insulin resistance ; Interferon ; Laboratories ; Lipids ; Liver ; Liver cirrhosis ; Liver diseases ; Medical ethics ; Medicine ; Medicine and Health Sciences ; Meta-analysis ; Metabolic disorders ; Metabolic syndrome ; Metabolic Syndrome - blood ; Metabolic Syndrome - epidemiology ; Metabolic syndrome X ; Metabolism ; Obesity ; Obesity, Abdominal - blood ; Obesity, Abdominal - epidemiology ; Observational studies ; Odds Ratio ; Offspring ; Physical Sciences ; Pregnancy ; Prevalence ; Prevalence studies (Epidemiology) ; Promoters ; Publication Bias ; Quality ; Quality control ; Research and Analysis Methods ; Risk analysis ; Risk assessment ; Risk factors ; Sensitivity analysis ; Statistical analysis ; Statistics ; Studies ; Subgroups ; Triglycerides ; Viruses</subject><ispartof>PloS one, 2017-05, Vol.12 (5), p.e0177713-e0177713</ispartof><rights>COPYRIGHT 2017 Public Library of Science</rights><rights>2017 Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2017 Li et al 2017 Li et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-1d5bb85907861c32dc5c95830465bf5c99d8493361f303d1825739a522da0d2a3</citedby><cites>FETCH-LOGICAL-c692t-1d5bb85907861c32dc5c95830465bf5c99d8493361f303d1825739a522da0d2a3</cites><orcidid>0000-0002-9363-3848</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1899014667/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1899014667?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28505202$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Bonino, Ferruccio</contributor><creatorcontrib>Li, Yuanyuan</creatorcontrib><creatorcontrib>Zhao, Ying</creatorcontrib><creatorcontrib>Wu, Jianping</creatorcontrib><title>Serum HBV surface antigen positivity is associated with low prevalence of metabolic syndrome: A meta-analysis</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>As there is conflicting evidence for the relationship between hepatitis B virus surface antigen (HBsAg) positivity and the prevalence of metabolic syndrome (MetS), we performed a meta-analysis to investigate whether HBsAg positivity affects the incidence of MetS.
Observational studies on the relationship between HBsAg positivity and MetS were obtained from PubMed, Web of Science, and the Cochrane Library in April 2016. The pooled odds ratios (ORs) of MetS and its components (central obesity, increased fasting glucose, increased blood pressure, dyslipidemia) for subjects with or without HBsAg positivity were synthesized. The standardized mean difference of MetS components between HBsAg-positive participants and healthy controls was calculated. Heterogeneity was explored with subgroup analysis and sensitivity analysis. Publication bias was detected using Egger's test and Begg's test.
Thirty studies were eligible for meta-analysis. The MetS OR for HBsAg-positive participants was significantly decreased compared with the controls [OR = 0.80, 95% confidence interval (CI), 0.70-0.90]. The negative effect of HBsAg positivity on elevated triglycerides (OR = 0.62, 95% CI, 0.59-0.64) was strong, while that for increased fasting blood glucose was weak (OR = 0.94, 95% CI, 0.90-0.98). The pooled ORs of central obesity (OR = 0.97, 95% CI, 0.91-1.04), reduced high-density lipoprotein cholesterol (OR = 0.98, 95% CI, 0.83-1.14), and elevated blood pressure (OR = 1.00, 95% CI, 0.80-1.25) for HBsAg-positive participants were all not significantly different compared with the controls. No publication bias was detected.
Serum HBsAg positivity is inversely associated with the prevalence of MetS. Among the five components of MetS, elevated triglycerides had the strongest inverse relationship with HBsAg positivity.</description><subject>Adiponectin</subject><subject>Age composition</subject><subject>Analysis</subject><subject>Antigens</subject><subject>Antiviral agents</subject><subject>Arteriosclerosis</subject><subject>Atherosclerosis</subject><subject>Bias</subject><subject>Biology and Life Sciences</subject><subject>Biomarkers</subject><subject>Blood</subject><subject>Blood pressure</subject><subject>Body mass</subject><subject>Body mass index</subject><subject>Cardiovascular diseases</subject><subject>Cholesterol</subject><subject>Chronic active hepatitis</subject><subject>Chronic infection</subject><subject>Cirrhosis</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Disease resistance</subject><subject>Dyslipidemia</subject><subject>Fasting</subject><subject>Glucose</subject><subject>Glucose metabolism</subject><subject>Heart diseases</subject><subject>Hepatitis</subject><subject>Hepatitis B surface antigen</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>Heterogeneity</subject><subject>Hospitals</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Incidence</subject><subject>Infections</subject><subject>Influence</subject><subject>Insulin</subject><subject>Insulin resistance</subject><subject>Interferon</subject><subject>Laboratories</subject><subject>Lipids</subject><subject>Liver</subject><subject>Liver cirrhosis</subject><subject>Liver diseases</subject><subject>Medical ethics</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Meta-analysis</subject><subject>Metabolic disorders</subject><subject>Metabolic syndrome</subject><subject>Metabolic Syndrome - blood</subject><subject>Metabolic Syndrome - epidemiology</subject><subject>Metabolic syndrome X</subject><subject>Metabolism</subject><subject>Obesity</subject><subject>Obesity, Abdominal - blood</subject><subject>Obesity, Abdominal - epidemiology</subject><subject>Observational studies</subject><subject>Odds Ratio</subject><subject>Offspring</subject><subject>Physical Sciences</subject><subject>Pregnancy</subject><subject>Prevalence</subject><subject>Prevalence studies (Epidemiology)</subject><subject>Promoters</subject><subject>Publication Bias</subject><subject>Quality</subject><subject>Quality control</subject><subject>Research and Analysis Methods</subject><subject>Risk analysis</subject><subject>Risk assessment</subject><subject>Risk factors</subject><subject>Sensitivity analysis</subject><subject>Statistical analysis</subject><subject>Statistics</subject><subject>Studies</subject><subject>Subgroups</subject><subject>Triglycerides</subject><subject>Viruses</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk11v0zAUhiMEYmPwDxBYQkJw0eKP2Im5QCoTsEqTJjHYreXaTuvJiTvb6ei_x12zqUG7QLmwffK87zk5zimK1whOEanQp2vfh0666dp3ZgpRVVWIPCmOESd4wjAkTw_2R8WLGK8hpKRm7HlxhGsKKYb4uGgvTehbcPb1CsQ-NFIZILtkl6YDax9tshubtsBGIGP0yspkNLi1aQWcvwXrYDbSmS6LfANak-TCO6tA3HY6-NZ8BrO76ETmQrfRxpfFs0a6aF4N60nx-_u3X6dnk_OLH_PT2flEMY7TBGm6WNSUw6pmSBGsFVWc1gSWjC6avOe6LjkhDDUEEo1qTCvCJcVYS6ixJCfF273v2vkohk5FgWrOISoZqzIx3xPay2uxDraVYSu8tOIu4MNSyJCsckYwI6lGXBPOy7JhFYdMkZooVOWTLHH2-jJk6xet0cp0KUg3Mh2_6exKLP1G0JLgXHw2-DAYBH_Tm5hEa6MyzsnO-H5fdwlLyHd1v_sHffzrBmqZr0fYrvE5r9qZilnJUcVQVZeZmj5C5Ueb1qr8WzU2x0eCjyNBZpL5k5ayj1HML3_-P3txNWbfH7ArI11aRe_6ZH0Xx2C5B1XwMQbTPDQZQbGbivtuiN1UiGEqsuzN4QU9iO7HgPwFHOoGZw</recordid><startdate>20170515</startdate><enddate>20170515</enddate><creator>Li, 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HBV surface antigen positivity is associated with low prevalence of metabolic syndrome: A meta-analysis</title><author>Li, Yuanyuan ; Zhao, Ying ; Wu, Jianping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-1d5bb85907861c32dc5c95830465bf5c99d8493361f303d1825739a522da0d2a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adiponectin</topic><topic>Age composition</topic><topic>Analysis</topic><topic>Antigens</topic><topic>Antiviral agents</topic><topic>Arteriosclerosis</topic><topic>Atherosclerosis</topic><topic>Bias</topic><topic>Biology and Life Sciences</topic><topic>Biomarkers</topic><topic>Blood</topic><topic>Blood pressure</topic><topic>Body mass</topic><topic>Body mass index</topic><topic>Cardiovascular diseases</topic><topic>Cholesterol</topic><topic>Chronic active hepatitis</topic><topic>Chronic infection</topic><topic>Cirrhosis</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Disease resistance</topic><topic>Dyslipidemia</topic><topic>Fasting</topic><topic>Glucose</topic><topic>Glucose metabolism</topic><topic>Heart diseases</topic><topic>Hepatitis</topic><topic>Hepatitis B surface antigen</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Heterogeneity</topic><topic>Hospitals</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Incidence</topic><topic>Infections</topic><topic>Influence</topic><topic>Insulin</topic><topic>Insulin resistance</topic><topic>Interferon</topic><topic>Laboratories</topic><topic>Lipids</topic><topic>Liver</topic><topic>Liver cirrhosis</topic><topic>Liver diseases</topic><topic>Medical ethics</topic><topic>Medicine</topic><topic>Medicine and Health Sciences</topic><topic>Meta-analysis</topic><topic>Metabolic disorders</topic><topic>Metabolic syndrome</topic><topic>Metabolic Syndrome - 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Ferruccio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum HBV surface antigen positivity is associated with low prevalence of metabolic syndrome: A meta-analysis</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2017-05-15</date><risdate>2017</risdate><volume>12</volume><issue>5</issue><spage>e0177713</spage><epage>e0177713</epage><pages>e0177713-e0177713</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>As there is conflicting evidence for the relationship between hepatitis B virus surface antigen (HBsAg) positivity and the prevalence of metabolic syndrome (MetS), we performed a meta-analysis to investigate whether HBsAg positivity affects the incidence of MetS.
Observational studies on the relationship between HBsAg positivity and MetS were obtained from PubMed, Web of Science, and the Cochrane Library in April 2016. The pooled odds ratios (ORs) of MetS and its components (central obesity, increased fasting glucose, increased blood pressure, dyslipidemia) for subjects with or without HBsAg positivity were synthesized. The standardized mean difference of MetS components between HBsAg-positive participants and healthy controls was calculated. Heterogeneity was explored with subgroup analysis and sensitivity analysis. Publication bias was detected using Egger's test and Begg's test.
Thirty studies were eligible for meta-analysis. The MetS OR for HBsAg-positive participants was significantly decreased compared with the controls [OR = 0.80, 95% confidence interval (CI), 0.70-0.90]. The negative effect of HBsAg positivity on elevated triglycerides (OR = 0.62, 95% CI, 0.59-0.64) was strong, while that for increased fasting blood glucose was weak (OR = 0.94, 95% CI, 0.90-0.98). The pooled ORs of central obesity (OR = 0.97, 95% CI, 0.91-1.04), reduced high-density lipoprotein cholesterol (OR = 0.98, 95% CI, 0.83-1.14), and elevated blood pressure (OR = 1.00, 95% CI, 0.80-1.25) for HBsAg-positive participants were all not significantly different compared with the controls. No publication bias was detected.
Serum HBsAg positivity is inversely associated with the prevalence of MetS. Among the five components of MetS, elevated triglycerides had the strongest inverse relationship with HBsAg positivity.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>28505202</pmid><doi>10.1371/journal.pone.0177713</doi><tpages>e0177713</tpages><orcidid>https://orcid.org/0000-0002-9363-3848</orcidid><oa>free_for_read</oa></addata></record> |
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ispartof | PloS one, 2017-05, Vol.12 (5), p.e0177713-e0177713 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_1899014667 |
source | Open Access: PubMed Central; Publicly Available Content Database |
subjects | Adiponectin Age composition Analysis Antigens Antiviral agents Arteriosclerosis Atherosclerosis Bias Biology and Life Sciences Biomarkers Blood Blood pressure Body mass Body mass index Cardiovascular diseases Cholesterol Chronic active hepatitis Chronic infection Cirrhosis Diabetes Diabetes mellitus Disease resistance Dyslipidemia Fasting Glucose Glucose metabolism Heart diseases Hepatitis Hepatitis B surface antigen Hepatitis B Surface Antigens - blood Heterogeneity Hospitals Humans Hypertension Incidence Infections Influence Insulin Insulin resistance Interferon Laboratories Lipids Liver Liver cirrhosis Liver diseases Medical ethics Medicine Medicine and Health Sciences Meta-analysis Metabolic disorders Metabolic syndrome Metabolic Syndrome - blood Metabolic Syndrome - epidemiology Metabolic syndrome X Metabolism Obesity Obesity, Abdominal - blood Obesity, Abdominal - epidemiology Observational studies Odds Ratio Offspring Physical Sciences Pregnancy Prevalence Prevalence studies (Epidemiology) Promoters Publication Bias Quality Quality control Research and Analysis Methods Risk analysis Risk assessment Risk factors Sensitivity analysis Statistical analysis Statistics Studies Subgroups Triglycerides Viruses |
title | Serum HBV surface antigen positivity is associated with low prevalence of metabolic syndrome: A meta-analysis |
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