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Metabolic Syndrome Components Are Associated with Intervertebral Disc Degeneration: The Wakayama Spine Study
The objective of the present study was to examine the associations between metabolic syndrome (MS) components, such as overweight (OW), hypertension (HT), dyslipidemia (DL), and impaired glucose tolerance (IGT), and intervertebral disc degeneration (DD). The present study included 928 participants (...
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Published in: | PloS one 2016-02, Vol.11 (2), p.e0147565-e0147565 |
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creator | Teraguchi, Masatoshi Yoshimura, Noriko Hashizume, Hiroshi Muraki, Shigeyuki Yamada, Hiroshi Oka, Hiroyuki Minamide, Akihito Ishimoto, Yuyu Nagata, Keiji Kagotani, Ryohei Tanaka, Sakae Kawaguchi, Hiroshi Nakamura, Kozo Akune, Toru Yoshida, Munehito |
description | The objective of the present study was to examine the associations between metabolic syndrome (MS) components, such as overweight (OW), hypertension (HT), dyslipidemia (DL), and impaired glucose tolerance (IGT), and intervertebral disc degeneration (DD).
The present study included 928 participants (308 men, 620 women) of the 1,011 participants in the Wakayama Spine Study. DD on magnetic resonance imaging was classified according to the Pfirrmann system. OW, HT, DL, and IGT were assessed using the criteria of the Examination Committee of Criteria for MS in Japan.
Multivariable logistic regression analysis revealed that OW was significantly associated with cervical, thoracic, and lumbar DD (cervical: odds ratio [OR], 1.28; 95% confidence interval [CI], 0.92-1.78; thoracic: OR, 1.75; 95% CI, 1.24-2.51; lumbar: OR, 1.87; 95% CI, 1.06-3.48). HT and IGT were significantly associated with thoracic DD (HT: OR, 1.54; 95% CI, 1.09-2.18; IGT: OR, 1.65; 95% CI, 1.12-2.48). Furthermore, subjects with 1 or more MS components had a higher OR for thoracic DD compared with those without MS components (vs. no component; 1 component: OR, 1.58; 95% CI, 1.03-2.42; 2 components: OR, 2.60; 95% CI, 1.62-4.20; ≥3 components: OR, 2.62; 95% CI, 1.42-5.00).
MS components were significantly associated with thoracic DD. Furthermore, accumulation of MS components significantly increased the OR for thoracic DD. These findings support the need for further studies of the effects of metabolic abnormality on DD. |
doi_str_mv | 10.1371/journal.pone.0147565 |
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The present study included 928 participants (308 men, 620 women) of the 1,011 participants in the Wakayama Spine Study. DD on magnetic resonance imaging was classified according to the Pfirrmann system. OW, HT, DL, and IGT were assessed using the criteria of the Examination Committee of Criteria for MS in Japan.
Multivariable logistic regression analysis revealed that OW was significantly associated with cervical, thoracic, and lumbar DD (cervical: odds ratio [OR], 1.28; 95% confidence interval [CI], 0.92-1.78; thoracic: OR, 1.75; 95% CI, 1.24-2.51; lumbar: OR, 1.87; 95% CI, 1.06-3.48). HT and IGT were significantly associated with thoracic DD (HT: OR, 1.54; 95% CI, 1.09-2.18; IGT: OR, 1.65; 95% CI, 1.12-2.48). Furthermore, subjects with 1 or more MS components had a higher OR for thoracic DD compared with those without MS components (vs. no component; 1 component: OR, 1.58; 95% CI, 1.03-2.42; 2 components: OR, 2.60; 95% CI, 1.62-4.20; ≥3 components: OR, 2.62; 95% CI, 1.42-5.00).
MS components were significantly associated with thoracic DD. Furthermore, accumulation of MS components significantly increased the OR for thoracic DD. These findings support the need for further studies of the effects of metabolic abnormality on DD.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0147565</identifier><identifier>PMID: 26840834</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Alcohol use ; Analysis ; Arthritis ; Atherosclerosis ; Back pain ; Biology and Life Sciences ; Biomarkers ; Blood Pressure ; Body weight ; Confidence intervals ; Criteria ; Degeneration ; Diabetes ; Disease ; Disease prevention ; Dyslipidemia ; Dyslipidemias ; Female ; Glucose ; Glucose Intolerance ; Glucose tolerance ; Hemoglobin ; Humans ; Hypertension ; Intervertebral Disc Degeneration - diagnosis ; Intervertebral Disc Degeneration - epidemiology ; Intervertebral Disc Degeneration - etiology ; Intervertebral discs ; Magnetic resonance ; Magnetic resonance imaging ; Male ; Medicine ; Medicine and Health Sciences ; Metabolic disorders ; Metabolic syndrome ; Metabolic Syndrome - complications ; Metabolic Syndrome - epidemiology ; Metabolic syndrome X ; Middle Aged ; Multivariate analysis ; NMR ; Nuclear magnetic resonance ; Obesity ; Odds Ratio ; Overweight ; People and Places ; People with disabilities ; Population ; Prevalence ; Regression analysis ; Rehabilitation ; Research and Analysis Methods ; Risk factors ; Spine ; Spine (lumbar) ; Spine - metabolism ; Spine - pathology ; Statistical analysis ; Studies ; Surgery ; Thorax ; Young Adult</subject><ispartof>PloS one, 2016-02, Vol.11 (2), p.e0147565-e0147565</ispartof><rights>COPYRIGHT 2016 Public Library of Science</rights><rights>2016 Teraguchi 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>2016 Teraguchi et al 2016 Teraguchi et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-40b8439b608e35e1ac544e24130312848c5b2d5221bed6887b418a6c3388bfc3</citedby><cites>FETCH-LOGICAL-c692t-40b8439b608e35e1ac544e24130312848c5b2d5221bed6887b418a6c3388bfc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1771248066/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1771248066?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26840834$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Katoh, Masaru</contributor><creatorcontrib>Teraguchi, Masatoshi</creatorcontrib><creatorcontrib>Yoshimura, Noriko</creatorcontrib><creatorcontrib>Hashizume, Hiroshi</creatorcontrib><creatorcontrib>Muraki, Shigeyuki</creatorcontrib><creatorcontrib>Yamada, Hiroshi</creatorcontrib><creatorcontrib>Oka, Hiroyuki</creatorcontrib><creatorcontrib>Minamide, Akihito</creatorcontrib><creatorcontrib>Ishimoto, Yuyu</creatorcontrib><creatorcontrib>Nagata, Keiji</creatorcontrib><creatorcontrib>Kagotani, Ryohei</creatorcontrib><creatorcontrib>Tanaka, Sakae</creatorcontrib><creatorcontrib>Kawaguchi, Hiroshi</creatorcontrib><creatorcontrib>Nakamura, Kozo</creatorcontrib><creatorcontrib>Akune, Toru</creatorcontrib><creatorcontrib>Yoshida, Munehito</creatorcontrib><title>Metabolic Syndrome Components Are Associated with Intervertebral Disc Degeneration: The Wakayama Spine Study</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The objective of the present study was to examine the associations between metabolic syndrome (MS) components, such as overweight (OW), hypertension (HT), dyslipidemia (DL), and impaired glucose tolerance (IGT), and intervertebral disc degeneration (DD).
The present study included 928 participants (308 men, 620 women) of the 1,011 participants in the Wakayama Spine Study. DD on magnetic resonance imaging was classified according to the Pfirrmann system. OW, HT, DL, and IGT were assessed using the criteria of the Examination Committee of Criteria for MS in Japan.
Multivariable logistic regression analysis revealed that OW was significantly associated with cervical, thoracic, and lumbar DD (cervical: odds ratio [OR], 1.28; 95% confidence interval [CI], 0.92-1.78; thoracic: OR, 1.75; 95% CI, 1.24-2.51; lumbar: OR, 1.87; 95% CI, 1.06-3.48). HT and IGT were significantly associated with thoracic DD (HT: OR, 1.54; 95% CI, 1.09-2.18; IGT: OR, 1.65; 95% CI, 1.12-2.48). Furthermore, subjects with 1 or more MS components had a higher OR for thoracic DD compared with those without MS components (vs. no component; 1 component: OR, 1.58; 95% CI, 1.03-2.42; 2 components: OR, 2.60; 95% CI, 1.62-4.20; ≥3 components: OR, 2.62; 95% CI, 1.42-5.00).
MS components were significantly associated with thoracic DD. Furthermore, accumulation of MS components significantly increased the OR for thoracic DD. These findings support the need for further studies of the effects of metabolic abnormality on DD.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alcohol use</subject><subject>Analysis</subject><subject>Arthritis</subject><subject>Atherosclerosis</subject><subject>Back pain</subject><subject>Biology and Life Sciences</subject><subject>Biomarkers</subject><subject>Blood Pressure</subject><subject>Body weight</subject><subject>Confidence intervals</subject><subject>Criteria</subject><subject>Degeneration</subject><subject>Diabetes</subject><subject>Disease</subject><subject>Disease prevention</subject><subject>Dyslipidemia</subject><subject>Dyslipidemias</subject><subject>Female</subject><subject>Glucose</subject><subject>Glucose Intolerance</subject><subject>Glucose tolerance</subject><subject>Hemoglobin</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Intervertebral Disc Degeneration - diagnosis</subject><subject>Intervertebral Disc Degeneration - epidemiology</subject><subject>Intervertebral Disc Degeneration - etiology</subject><subject>Intervertebral discs</subject><subject>Magnetic resonance</subject><subject>Magnetic resonance imaging</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine and Health Sciences</subject><subject>Metabolic disorders</subject><subject>Metabolic syndrome</subject><subject>Metabolic Syndrome - complications</subject><subject>Metabolic Syndrome - epidemiology</subject><subject>Metabolic syndrome X</subject><subject>Middle Aged</subject><subject>Multivariate analysis</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Obesity</subject><subject>Odds Ratio</subject><subject>Overweight</subject><subject>People and Places</subject><subject>People with disabilities</subject><subject>Population</subject><subject>Prevalence</subject><subject>Regression analysis</subject><subject>Rehabilitation</subject><subject>Research and Analysis Methods</subject><subject>Risk factors</subject><subject>Spine</subject><subject>Spine (lumbar)</subject><subject>Spine - metabolism</subject><subject>Spine - pathology</subject><subject>Statistical analysis</subject><subject>Studies</subject><subject>Surgery</subject><subject>Thorax</subject><subject>Young Adult</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNk11v0zAUhiMEYmPwDxBEQkJw0eKvOM4ukKqOj0pDk2gFl5bjnLQeSVxsZ9B_j0OzqUW7QL6wdfyc99ivfZLkOUZTTHP87tr2rlPNdGs7mCLM8oxnD5JTXFAy4QTRhwfrk-SJ99cIZVRw_jg5IVwwJCg7TZovEFRpG6PT5a6rnG0hndt2EO2CT2cO0pn3VhsVoEp_mbBJF10AdwMuQOlUk14Yr9MLWEMHTgVju_N0tYH0u_qhdqpV6XJrOkiXoa92T5NHtWo8PBvns2T18cNq_nlyefVpMZ9dTjQvSJgwVApGi5IjATQDrHTGGBCGKaKYCCZ0VpIqIwSXUHEh8pJhobimVIiy1vQsebmX3TbWy9EnL3GeY8IE4jwSiz1RWXUtt860yu2kVUb-DVi3lsoFoxuQnApaa8hQXdWMF4NxecVyhViNaCaqqPV-rNaXLVQ6-hZtORI93unMRq7tjWQ5LXKKo8CbUcDZnz34INtoKTSN6sD2w7k5KXiGEYnoq3_Q-283UmsVL2C62sa6ehCVM8YIzhHLhrLTe6g4KmiNju9fmxg_Snh7lBCZAL_DWvXey8Xy6_-zV9-O2dcH7AZUEzbeNv3wl_wxyPagdtZ7B_WdyRjJoSdu3ZDD95VjT8S0F4cPdJd02wT0D-LjBYg</recordid><startdate>20160203</startdate><enddate>20160203</enddate><creator>Teraguchi, Masatoshi</creator><creator>Yoshimura, Noriko</creator><creator>Hashizume, Hiroshi</creator><creator>Muraki, Shigeyuki</creator><creator>Yamada, Hiroshi</creator><creator>Oka, Hiroyuki</creator><creator>Minamide, Akihito</creator><creator>Ishimoto, Yuyu</creator><creator>Nagata, Keiji</creator><creator>Kagotani, Ryohei</creator><creator>Tanaka, Sakae</creator><creator>Kawaguchi, Hiroshi</creator><creator>Nakamura, Kozo</creator><creator>Akune, Toru</creator><creator>Yoshida, Munehito</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20160203</creationdate><title>Metabolic Syndrome Components Are Associated with Intervertebral Disc Degeneration: The Wakayama Spine Study</title><author>Teraguchi, Masatoshi ; Yoshimura, Noriko ; Hashizume, Hiroshi ; Muraki, Shigeyuki ; Yamada, Hiroshi ; Oka, Hiroyuki ; Minamide, Akihito ; Ishimoto, Yuyu ; Nagata, Keiji ; Kagotani, Ryohei ; Tanaka, Sakae ; Kawaguchi, Hiroshi ; Nakamura, Kozo ; Akune, Toru ; Yoshida, Munehito</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-40b8439b608e35e1ac544e24130312848c5b2d5221bed6887b418a6c3388bfc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alcohol use</topic><topic>Analysis</topic><topic>Arthritis</topic><topic>Atherosclerosis</topic><topic>Back pain</topic><topic>Biology and Life Sciences</topic><topic>Biomarkers</topic><topic>Blood Pressure</topic><topic>Body weight</topic><topic>Confidence intervals</topic><topic>Criteria</topic><topic>Degeneration</topic><topic>Diabetes</topic><topic>Disease</topic><topic>Disease prevention</topic><topic>Dyslipidemia</topic><topic>Dyslipidemias</topic><topic>Female</topic><topic>Glucose</topic><topic>Glucose Intolerance</topic><topic>Glucose tolerance</topic><topic>Hemoglobin</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Intervertebral Disc Degeneration - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Teraguchi, Masatoshi</au><au>Yoshimura, Noriko</au><au>Hashizume, Hiroshi</au><au>Muraki, Shigeyuki</au><au>Yamada, Hiroshi</au><au>Oka, Hiroyuki</au><au>Minamide, Akihito</au><au>Ishimoto, Yuyu</au><au>Nagata, Keiji</au><au>Kagotani, Ryohei</au><au>Tanaka, Sakae</au><au>Kawaguchi, Hiroshi</au><au>Nakamura, Kozo</au><au>Akune, Toru</au><au>Yoshida, Munehito</au><au>Katoh, Masaru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic Syndrome Components Are Associated with Intervertebral Disc Degeneration: The Wakayama Spine Study</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2016-02-03</date><risdate>2016</risdate><volume>11</volume><issue>2</issue><spage>e0147565</spage><epage>e0147565</epage><pages>e0147565-e0147565</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The objective of the present study was to examine the associations between metabolic syndrome (MS) components, such as overweight (OW), hypertension (HT), dyslipidemia (DL), and impaired glucose tolerance (IGT), and intervertebral disc degeneration (DD).
The present study included 928 participants (308 men, 620 women) of the 1,011 participants in the Wakayama Spine Study. DD on magnetic resonance imaging was classified according to the Pfirrmann system. OW, HT, DL, and IGT were assessed using the criteria of the Examination Committee of Criteria for MS in Japan.
Multivariable logistic regression analysis revealed that OW was significantly associated with cervical, thoracic, and lumbar DD (cervical: odds ratio [OR], 1.28; 95% confidence interval [CI], 0.92-1.78; thoracic: OR, 1.75; 95% CI, 1.24-2.51; lumbar: OR, 1.87; 95% CI, 1.06-3.48). HT and IGT were significantly associated with thoracic DD (HT: OR, 1.54; 95% CI, 1.09-2.18; IGT: OR, 1.65; 95% CI, 1.12-2.48). Furthermore, subjects with 1 or more MS components had a higher OR for thoracic DD compared with those without MS components (vs. no component; 1 component: OR, 1.58; 95% CI, 1.03-2.42; 2 components: OR, 2.60; 95% CI, 1.62-4.20; ≥3 components: OR, 2.62; 95% CI, 1.42-5.00).
MS components were significantly associated with thoracic DD. Furthermore, accumulation of MS components significantly increased the OR for thoracic DD. These findings support the need for further studies of the effects of metabolic abnormality on DD.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26840834</pmid><doi>10.1371/journal.pone.0147565</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
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issn | 1932-6203 1932-6203 |
language | eng |
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source | Publicly Available Content Database; PubMed Central |
subjects | Adult Aged Aged, 80 and over Alcohol use Analysis Arthritis Atherosclerosis Back pain Biology and Life Sciences Biomarkers Blood Pressure Body weight Confidence intervals Criteria Degeneration Diabetes Disease Disease prevention Dyslipidemia Dyslipidemias Female Glucose Glucose Intolerance Glucose tolerance Hemoglobin Humans Hypertension Intervertebral Disc Degeneration - diagnosis Intervertebral Disc Degeneration - epidemiology Intervertebral Disc Degeneration - etiology Intervertebral discs Magnetic resonance Magnetic resonance imaging Male Medicine Medicine and Health Sciences Metabolic disorders Metabolic syndrome Metabolic Syndrome - complications Metabolic Syndrome - epidemiology Metabolic syndrome X Middle Aged Multivariate analysis NMR Nuclear magnetic resonance Obesity Odds Ratio Overweight People and Places People with disabilities Population Prevalence Regression analysis Rehabilitation Research and Analysis Methods Risk factors Spine Spine (lumbar) Spine - metabolism Spine - pathology Statistical analysis Studies Surgery Thorax Young Adult |
title | Metabolic Syndrome Components Are Associated with Intervertebral Disc Degeneration: The Wakayama Spine Study |
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