A case-control study to assess possible triggers and cofactors in chronic fatigue syndrome
To assess possible triggers and cofactors for chronic fatigue syndrome (CFS) and to compare levels of selected cytokines between cases and an appropriately matched control group. We Conducted a casecontrol study of 47 cases of CFS obtained through a regional CFS research program maintained at a tert...
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Veröffentlicht in: | The American journal of medicine 1996-05, Vol.100 (5), p.548-554 |
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creator | MacDonald, Kristine L. Osterholm, Michael T. LeDell, Kathleen H. White, Karen E. Schenck, Carlos H. Chao, Chun C. Persing, David H. Johnson, Russell C. Barker, James M. Peterson, Phillip K. |
description | To assess possible triggers and cofactors for chronic fatigue syndrome (CFS) and to compare levels of selected cytokines between cases and an appropriately matched control group.
We Conducted a casecontrol study of 47 cases of CFS obtained through a regional CFS research program maintained at a tertiary care medical center. One age-, gender-, and neighborhood-matched control was identified for each case through systematic community telephone sampling. Standardized questionnaires were administered to cases and controls. Sera were assayed for transforming growth factor-
β (TGF-
β), interleukin-1
β, interleukin-6, tumor necrosis factor-
α, and antibody to
Borrelia burgdorferi and
Babesia microti.
Cases were more likely to have exercised regularly before illness onset than controls (67% versus 40%; matched odds ratio (MOR) = 3.4; 95% Cl = 1.2 to 11.8;
P = 0.02). Female cases were more likely to be nulliparous prior to onset of CFS than controls (51% versus 31%; MOR = 8.0; 95% Cl = 1.03 to 170;
P = 0.05). History of other major factors, including silicone-gel breast implants (one female case and one female control), pre-morbid history of depression (15% of cases, 11% of controls) and history of allergies (66% of cases, 51% of controls) were similar for cases and controls. However, cases were more likely to have a diagnosis of depression subsequent to their diagnosis of CFS compared to a similar time frame for controls (MOR = undefined; 95% Cl lower bound = 2.5;
P < 0.001). Positive antibody titers to
B burgdorferi (one case and one control) and
B microti (zero cases and two controls) were also similar.
Further investigation into the role of prior routine exercise as a cofactor for CFS is warranted. This study supports the concurrence of CFS and depression, although pre-morbid history of depression was similar for both groups. |
doi_str_mv | 10.1016/S0002-9343(96)00017-4 |
format | Article |
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We Conducted a casecontrol study of 47 cases of CFS obtained through a regional CFS research program maintained at a tertiary care medical center. One age-, gender-, and neighborhood-matched control was identified for each case through systematic community telephone sampling. Standardized questionnaires were administered to cases and controls. Sera were assayed for transforming growth factor-
β (TGF-
β), interleukin-1
β, interleukin-6, tumor necrosis factor-
α, and antibody to
Borrelia burgdorferi and
Babesia microti.
Cases were more likely to have exercised regularly before illness onset than controls (67% versus 40%; matched odds ratio (MOR) = 3.4; 95% Cl = 1.2 to 11.8;
P = 0.02). Female cases were more likely to be nulliparous prior to onset of CFS than controls (51% versus 31%; MOR = 8.0; 95% Cl = 1.03 to 170;
P = 0.05). History of other major factors, including silicone-gel breast implants (one female case and one female control), pre-morbid history of depression (15% of cases, 11% of controls) and history of allergies (66% of cases, 51% of controls) were similar for cases and controls. However, cases were more likely to have a diagnosis of depression subsequent to their diagnosis of CFS compared to a similar time frame for controls (MOR = undefined; 95% Cl lower bound = 2.5;
P < 0.001). Positive antibody titers to
B burgdorferi (one case and one control) and
B microti (zero cases and two controls) were also similar.
Further investigation into the role of prior routine exercise as a cofactor for CFS is warranted. This study supports the concurrence of CFS and depression, although pre-morbid history of depression was similar for both groups.</description><identifier>ISSN: 0002-9343</identifier><identifier>EISSN: 1555-7162</identifier><identifier>DOI: 10.1016/S0002-9343(96)00017-4</identifier><identifier>PMID: 8644768</identifier><identifier>CODEN: AJMEAZ</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Aged ; Animals ; Antibodies, Bacterial - analysis ; Antibodies, Protozoan - analysis ; Babesia - immunology ; Biological and medical sciences ; Borrelia burgdorferi Group - immunology ; Case-Control Studies ; Chronic fatigue syndrome ; Chronic illnesses ; Data Interpretation, Statistical ; Depression - complications ; Fatigue ; Fatigue Syndrome, Chronic - blood ; Fatigue Syndrome, Chronic - etiology ; Female ; Humans ; Hypersensitivity - complications ; Interleukin-1 - blood ; Interleukin-6 - blood ; Male ; Medical research ; Medical sciences ; Mental depression ; Middle Aged ; Parity ; Physical Exertion ; Risk Factors ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Surveys and Questionnaires ; Time Factors ; Transforming Growth Factor beta - blood ; Tumor Necrosis Factor-alpha - analysis</subject><ispartof>The American journal of medicine, 1996-05, Vol.100 (5), p.548-554</ispartof><rights>1996 Excerpta Medica, Inc. All rights reserved</rights><rights>1996 INIST-CNRS</rights><rights>Copyright Elsevier Sequoia S.A. May 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-551802b576ddeae0cb6cb6ac09b8c1055b9b754cf127e6e694d38cc795d987e13</citedby><cites>FETCH-LOGICAL-c416t-551802b576ddeae0cb6cb6ac09b8c1055b9b754cf127e6e694d38cc795d987e13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0002-9343(96)00017-4$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3115002$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8644768$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MacDonald, Kristine L.</creatorcontrib><creatorcontrib>Osterholm, Michael T.</creatorcontrib><creatorcontrib>LeDell, Kathleen H.</creatorcontrib><creatorcontrib>White, Karen E.</creatorcontrib><creatorcontrib>Schenck, Carlos H.</creatorcontrib><creatorcontrib>Chao, Chun C.</creatorcontrib><creatorcontrib>Persing, David H.</creatorcontrib><creatorcontrib>Johnson, Russell C.</creatorcontrib><creatorcontrib>Barker, James M.</creatorcontrib><creatorcontrib>Peterson, Phillip K.</creatorcontrib><title>A case-control study to assess possible triggers and cofactors in chronic fatigue syndrome</title><title>The American journal of medicine</title><addtitle>Am J Med</addtitle><description>To assess possible triggers and cofactors for chronic fatigue syndrome (CFS) and to compare levels of selected cytokines between cases and an appropriately matched control group.
We Conducted a casecontrol study of 47 cases of CFS obtained through a regional CFS research program maintained at a tertiary care medical center. One age-, gender-, and neighborhood-matched control was identified for each case through systematic community telephone sampling. Standardized questionnaires were administered to cases and controls. Sera were assayed for transforming growth factor-
β (TGF-
β), interleukin-1
β, interleukin-6, tumor necrosis factor-
α, and antibody to
Borrelia burgdorferi and
Babesia microti.
Cases were more likely to have exercised regularly before illness onset than controls (67% versus 40%; matched odds ratio (MOR) = 3.4; 95% Cl = 1.2 to 11.8;
P = 0.02). Female cases were more likely to be nulliparous prior to onset of CFS than controls (51% versus 31%; MOR = 8.0; 95% Cl = 1.03 to 170;
P = 0.05). History of other major factors, including silicone-gel breast implants (one female case and one female control), pre-morbid history of depression (15% of cases, 11% of controls) and history of allergies (66% of cases, 51% of controls) were similar for cases and controls. However, cases were more likely to have a diagnosis of depression subsequent to their diagnosis of CFS compared to a similar time frame for controls (MOR = undefined; 95% Cl lower bound = 2.5;
P < 0.001). Positive antibody titers to
B burgdorferi (one case and one control) and
B microti (zero cases and two controls) were also similar.
Further investigation into the role of prior routine exercise as a cofactor for CFS is warranted. This study supports the concurrence of CFS and depression, although pre-morbid history of depression was similar for both groups.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Animals</subject><subject>Antibodies, Bacterial - analysis</subject><subject>Antibodies, Protozoan - analysis</subject><subject>Babesia - immunology</subject><subject>Biological and medical sciences</subject><subject>Borrelia burgdorferi Group - immunology</subject><subject>Case-Control Studies</subject><subject>Chronic fatigue syndrome</subject><subject>Chronic illnesses</subject><subject>Data Interpretation, Statistical</subject><subject>Depression - complications</subject><subject>Fatigue</subject><subject>Fatigue Syndrome, Chronic - blood</subject><subject>Fatigue Syndrome, Chronic - etiology</subject><subject>Female</subject><subject>Humans</subject><subject>Hypersensitivity - complications</subject><subject>Interleukin-1 - blood</subject><subject>Interleukin-6 - blood</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Mental depression</subject><subject>Middle Aged</subject><subject>Parity</subject><subject>Physical Exertion</subject><subject>Risk Factors</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Surveys and Questionnaires</subject><subject>Time Factors</subject><subject>Transforming Growth Factor beta - blood</subject><subject>Tumor Necrosis Factor-alpha - analysis</subject><issn>0002-9343</issn><issn>1555-7162</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkFFrFDEQx4Mo9Vr9CIUgIvVha7K7yW6eSilqCwUfqi--hOxk9kzZS87MrnDf3rR33IMvQiD8md8MMz_GzqW4lELqTw9CiLoyTdtcGP2xBNlV7Qu2kkqpqpO6fslWR-Q1OyV6LFEYpU_YSa_bttP9iv285uAIK0hxzmniNC9-x-fEHRES8W0iCsOEfM5hvcZM3EXPIY0O5lRSiBx-5RQD8NHNYb0gp130OW3wDXs1uonw7eE_Yz--fP5-c1vdf_t6d3N9X0Er9VwpJXtRD6rT3qNDAYMuz4EwQw9SKDWYoVMtjLLuUKM2rW96gM4ob_oOZXPGPuznbnP6vSDNdhMIcJpcxLSQ7XqhZa10Ad_9Az6mJceym62bulGN1KJAag9BLqdnHO02h43LOyuFfRJvn8XbJ6vWaPss3ral7_wwfBk26I9dB9Ol_v5QdwRuGrOLEOiINVKqMrZgV3sMi7E_AbMlCBgBfcgIs_Up_GeRv6IinyU</recordid><startdate>19960501</startdate><enddate>19960501</enddate><creator>MacDonald, Kristine L.</creator><creator>Osterholm, Michael T.</creator><creator>LeDell, Kathleen H.</creator><creator>White, Karen E.</creator><creator>Schenck, Carlos H.</creator><creator>Chao, Chun C.</creator><creator>Persing, David H.</creator><creator>Johnson, Russell C.</creator><creator>Barker, James M.</creator><creator>Peterson, Phillip K.</creator><general>Elsevier Inc</general><general>Elsevier</general><general>Elsevier Sequoia S.A</general><scope>IQODW</scope><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>7T5</scope><scope>7TK</scope><scope>7TO</scope><scope>7TS</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>19960501</creationdate><title>A case-control study to assess possible triggers and cofactors in chronic fatigue syndrome</title><author>MacDonald, Kristine L. ; Osterholm, Michael T. ; LeDell, Kathleen H. ; White, Karen E. ; Schenck, Carlos H. ; Chao, Chun C. ; Persing, David H. ; Johnson, Russell C. ; Barker, James M. ; Peterson, Phillip K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-551802b576ddeae0cb6cb6ac09b8c1055b9b754cf127e6e694d38cc795d987e13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Animals</topic><topic>Antibodies, Bacterial - analysis</topic><topic>Antibodies, Protozoan - analysis</topic><topic>Babesia - immunology</topic><topic>Biological and medical sciences</topic><topic>Borrelia burgdorferi Group - immunology</topic><topic>Case-Control Studies</topic><topic>Chronic fatigue syndrome</topic><topic>Chronic illnesses</topic><topic>Data Interpretation, Statistical</topic><topic>Depression - complications</topic><topic>Fatigue</topic><topic>Fatigue Syndrome, Chronic - blood</topic><topic>Fatigue Syndrome, Chronic - etiology</topic><topic>Female</topic><topic>Humans</topic><topic>Hypersensitivity - complications</topic><topic>Interleukin-1 - blood</topic><topic>Interleukin-6 - blood</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Mental depression</topic><topic>Middle Aged</topic><topic>Parity</topic><topic>Physical Exertion</topic><topic>Risk Factors</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Surveys and Questionnaires</topic><topic>Time Factors</topic><topic>Transforming Growth Factor beta - blood</topic><topic>Tumor Necrosis Factor-alpha - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MacDonald, Kristine L.</creatorcontrib><creatorcontrib>Osterholm, Michael T.</creatorcontrib><creatorcontrib>LeDell, Kathleen H.</creatorcontrib><creatorcontrib>White, Karen E.</creatorcontrib><creatorcontrib>Schenck, Carlos H.</creatorcontrib><creatorcontrib>Chao, Chun C.</creatorcontrib><creatorcontrib>Persing, David H.</creatorcontrib><creatorcontrib>Johnson, Russell C.</creatorcontrib><creatorcontrib>Barker, James M.</creatorcontrib><creatorcontrib>Peterson, Phillip K.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Physical Education Index</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MacDonald, Kristine L.</au><au>Osterholm, Michael T.</au><au>LeDell, Kathleen H.</au><au>White, Karen E.</au><au>Schenck, Carlos H.</au><au>Chao, Chun C.</au><au>Persing, David H.</au><au>Johnson, Russell C.</au><au>Barker, James M.</au><au>Peterson, Phillip K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A case-control study to assess possible triggers and cofactors in chronic fatigue syndrome</atitle><jtitle>The American journal of medicine</jtitle><addtitle>Am J Med</addtitle><date>1996-05-01</date><risdate>1996</risdate><volume>100</volume><issue>5</issue><spage>548</spage><epage>554</epage><pages>548-554</pages><issn>0002-9343</issn><eissn>1555-7162</eissn><coden>AJMEAZ</coden><abstract>To assess possible triggers and cofactors for chronic fatigue syndrome (CFS) and to compare levels of selected cytokines between cases and an appropriately matched control group.
We Conducted a casecontrol study of 47 cases of CFS obtained through a regional CFS research program maintained at a tertiary care medical center. One age-, gender-, and neighborhood-matched control was identified for each case through systematic community telephone sampling. Standardized questionnaires were administered to cases and controls. Sera were assayed for transforming growth factor-
β (TGF-
β), interleukin-1
β, interleukin-6, tumor necrosis factor-
α, and antibody to
Borrelia burgdorferi and
Babesia microti.
Cases were more likely to have exercised regularly before illness onset than controls (67% versus 40%; matched odds ratio (MOR) = 3.4; 95% Cl = 1.2 to 11.8;
P = 0.02). Female cases were more likely to be nulliparous prior to onset of CFS than controls (51% versus 31%; MOR = 8.0; 95% Cl = 1.03 to 170;
P = 0.05). History of other major factors, including silicone-gel breast implants (one female case and one female control), pre-morbid history of depression (15% of cases, 11% of controls) and history of allergies (66% of cases, 51% of controls) were similar for cases and controls. However, cases were more likely to have a diagnosis of depression subsequent to their diagnosis of CFS compared to a similar time frame for controls (MOR = undefined; 95% Cl lower bound = 2.5;
P < 0.001). Positive antibody titers to
B burgdorferi (one case and one control) and
B microti (zero cases and two controls) were also similar.
Further investigation into the role of prior routine exercise as a cofactor for CFS is warranted. This study supports the concurrence of CFS and depression, although pre-morbid history of depression was similar for both groups.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>8644768</pmid><doi>10.1016/S0002-9343(96)00017-4</doi><tpages>7</tpages></addata></record> |
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language | eng |
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source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Adolescent Adult Aged Animals Antibodies, Bacterial - analysis Antibodies, Protozoan - analysis Babesia - immunology Biological and medical sciences Borrelia burgdorferi Group - immunology Case-Control Studies Chronic fatigue syndrome Chronic illnesses Data Interpretation, Statistical Depression - complications Fatigue Fatigue Syndrome, Chronic - blood Fatigue Syndrome, Chronic - etiology Female Humans Hypersensitivity - complications Interleukin-1 - blood Interleukin-6 - blood Male Medical research Medical sciences Mental depression Middle Aged Parity Physical Exertion Risk Factors Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Surveys and Questionnaires Time Factors Transforming Growth Factor beta - blood Tumor Necrosis Factor-alpha - analysis |
title | A case-control study to assess possible triggers and cofactors in chronic fatigue syndrome |
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