Associations Between Fibrin D-Dimer, Markers of Inflammation, Incident Self-Reported Mobility Limitation, and All-Cause Mortality in Older Men

Objectives To examine the independent relationships between fibrin D‐dimer, interleukin 6 (IL‐6), C‐reactive protein (CRP), and fibrinogen and incident mobility limitation and mortality. Design Prospective. Setting General practice in 24 British towns. Participants Men aged 60 to 79 without prevalen...

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Veröffentlicht in:Journal of the American Geriatrics Society (JAGS) 2014-12, Vol.62 (12), p.2357-2362
Hauptverfasser: Wannamethee, S. Goya, Whincup, Peter H., Lennon, Lucy, Papacosta, Olia, Lowe, Gordon D.
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container_issue 12
container_start_page 2357
container_title Journal of the American Geriatrics Society (JAGS)
container_volume 62
creator Wannamethee, S. Goya
Whincup, Peter H.
Lennon, Lucy
Papacosta, Olia
Lowe, Gordon D.
description Objectives To examine the independent relationships between fibrin D‐dimer, interleukin 6 (IL‐6), C‐reactive protein (CRP), and fibrinogen and incident mobility limitation and mortality. Design Prospective. Setting General practice in 24 British towns. Participants Men aged 60 to 79 without prevalent heart failure followed up for an average of 11.5 years (N = 3,925). Measurements All‐cause mortality (n = 1,286) and self‐reported mobility disability obtained at examination in 1998 to 2000 and in a postal questionnaire 3 to 5 years later in 2003. Results High D‐dimer (top vs lowest tertile: adjusted odds ratio (aOR) = 1.46, 95% confidence interval = 1.02–2.05) and IL‐6 (aOR = 1.43, 95% CI = 1.01–2.02) levels (but not CRP or fibrinogen) were associated with greater incident mobility limitation after adjustment for confounders and prevalent disease status. IL‐6, CRP, fibrinogen, and D‐dimer were significantly associated with total mortality after adjustment for confounders. Only D‐dimer and IL‐6 predicted total mortality independent of each other and the other biomarkers. The adjusted hazard ratio (aHR) was 1.16 (95% CI = 1.10–1.22) for a standard deviation increase in log D‐dimer and 1.10 (95% CI = 1.04–1.18) for a standard deviation increase in log IL‐6. D‐dimer was independently related to vascular and nonvascular mortality, and IL‐6 was independently related to vascular mortality. Risks of mobility limitation and mortality were greatest in those with a combination of high D‐dimer and IL‐6 levels. Conclusion D‐dimer and IL‐6 are associated with risk of mobility limitation and mortality in older men without heart failure. The findings suggest that coagulation leads to functional decline and mortality s that inflammation does not explain.
doi_str_mv 10.1111/jgs.13133
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Goya ; Whincup, Peter H. ; Lennon, Lucy ; Papacosta, Olia ; Lowe, Gordon D.</creator><creatorcontrib>Wannamethee, S. Goya ; Whincup, Peter H. ; Lennon, Lucy ; Papacosta, Olia ; Lowe, Gordon D.</creatorcontrib><description>Objectives To examine the independent relationships between fibrin D‐dimer, interleukin 6 (IL‐6), C‐reactive protein (CRP), and fibrinogen and incident mobility limitation and mortality. Design Prospective. Setting General practice in 24 British towns. Participants Men aged 60 to 79 without prevalent heart failure followed up for an average of 11.5 years (N = 3,925). Measurements All‐cause mortality (n = 1,286) and self‐reported mobility disability obtained at examination in 1998 to 2000 and in a postal questionnaire 3 to 5 years later in 2003. Results High D‐dimer (top vs lowest tertile: adjusted odds ratio (aOR) = 1.46, 95% confidence interval = 1.02–2.05) and IL‐6 (aOR = 1.43, 95% CI = 1.01–2.02) levels (but not CRP or fibrinogen) were associated with greater incident mobility limitation after adjustment for confounders and prevalent disease status. IL‐6, CRP, fibrinogen, and D‐dimer were significantly associated with total mortality after adjustment for confounders. Only D‐dimer and IL‐6 predicted total mortality independent of each other and the other biomarkers. The adjusted hazard ratio (aHR) was 1.16 (95% CI = 1.10–1.22) for a standard deviation increase in log D‐dimer and 1.10 (95% CI = 1.04–1.18) for a standard deviation increase in log IL‐6. D‐dimer was independently related to vascular and nonvascular mortality, and IL‐6 was independently related to vascular mortality. Risks of mobility limitation and mortality were greatest in those with a combination of high D‐dimer and IL‐6 levels. Conclusion D‐dimer and IL‐6 are associated with risk of mobility limitation and mortality in older men without heart failure. The findings suggest that coagulation leads to functional decline and mortality s that inflammation does not explain.</description><identifier>ISSN: 0002-8614</identifier><identifier>EISSN: 1532-5415</identifier><identifier>DOI: 10.1111/jgs.13133</identifier><identifier>PMID: 25516032</identifier><identifier>CODEN: JAGSAF</identifier><language>eng</language><publisher>Hoboken, NJ: Blackwell Publishing Ltd</publisher><subject>Aged ; Biological and medical sciences ; Brief Reports ; C-Reactive Protein - metabolism ; Cause of Death ; Coagulation ; D-dimer ; England - epidemiology ; Enzyme-Linked Immunosorbent Assay ; Epidemiology ; Fibrin Fibrinogen Degradation Products - metabolism ; General aspects ; Geriatrics ; Humans ; inflammation ; Inflammation - blood ; Interleukin-6 - blood ; Male ; Medical sciences ; Mens health ; Middle Aged ; Miscellaneous ; Mobility Limitation ; Mortality ; Prospective Studies ; Public health. Hygiene ; Public health. 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Goya</creatorcontrib><creatorcontrib>Whincup, Peter H.</creatorcontrib><creatorcontrib>Lennon, Lucy</creatorcontrib><creatorcontrib>Papacosta, Olia</creatorcontrib><creatorcontrib>Lowe, Gordon D.</creatorcontrib><title>Associations Between Fibrin D-Dimer, Markers of Inflammation, Incident Self-Reported Mobility Limitation, and All-Cause Mortality in Older Men</title><title>Journal of the American Geriatrics Society (JAGS)</title><addtitle>J Am Geriatr Soc</addtitle><description>Objectives To examine the independent relationships between fibrin D‐dimer, interleukin 6 (IL‐6), C‐reactive protein (CRP), and fibrinogen and incident mobility limitation and mortality. Design Prospective. Setting General practice in 24 British towns. Participants Men aged 60 to 79 without prevalent heart failure followed up for an average of 11.5 years (N = 3,925). Measurements All‐cause mortality (n = 1,286) and self‐reported mobility disability obtained at examination in 1998 to 2000 and in a postal questionnaire 3 to 5 years later in 2003. Results High D‐dimer (top vs lowest tertile: adjusted odds ratio (aOR) = 1.46, 95% confidence interval = 1.02–2.05) and IL‐6 (aOR = 1.43, 95% CI = 1.01–2.02) levels (but not CRP or fibrinogen) were associated with greater incident mobility limitation after adjustment for confounders and prevalent disease status. IL‐6, CRP, fibrinogen, and D‐dimer were significantly associated with total mortality after adjustment for confounders. Only D‐dimer and IL‐6 predicted total mortality independent of each other and the other biomarkers. The adjusted hazard ratio (aHR) was 1.16 (95% CI = 1.10–1.22) for a standard deviation increase in log D‐dimer and 1.10 (95% CI = 1.04–1.18) for a standard deviation increase in log IL‐6. D‐dimer was independently related to vascular and nonvascular mortality, and IL‐6 was independently related to vascular mortality. Risks of mobility limitation and mortality were greatest in those with a combination of high D‐dimer and IL‐6 levels. Conclusion D‐dimer and IL‐6 are associated with risk of mobility limitation and mortality in older men without heart failure. 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Goya</creatorcontrib><creatorcontrib>Whincup, Peter H.</creatorcontrib><creatorcontrib>Lennon, Lucy</creatorcontrib><creatorcontrib>Papacosta, Olia</creatorcontrib><creatorcontrib>Lowe, Gordon D.</creatorcontrib><collection>Istex</collection><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Free Content</collection><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>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the American Geriatrics Society (JAGS)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wannamethee, S. Goya</au><au>Whincup, Peter H.</au><au>Lennon, Lucy</au><au>Papacosta, Olia</au><au>Lowe, Gordon D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Associations Between Fibrin D-Dimer, Markers of Inflammation, Incident Self-Reported Mobility Limitation, and All-Cause Mortality in Older Men</atitle><jtitle>Journal of the American Geriatrics Society (JAGS)</jtitle><addtitle>J Am Geriatr Soc</addtitle><date>2014-12</date><risdate>2014</risdate><volume>62</volume><issue>12</issue><spage>2357</spage><epage>2362</epage><pages>2357-2362</pages><issn>0002-8614</issn><eissn>1532-5415</eissn><coden>JAGSAF</coden><abstract>Objectives To examine the independent relationships between fibrin D‐dimer, interleukin 6 (IL‐6), C‐reactive protein (CRP), and fibrinogen and incident mobility limitation and mortality. Design Prospective. Setting General practice in 24 British towns. Participants Men aged 60 to 79 without prevalent heart failure followed up for an average of 11.5 years (N = 3,925). Measurements All‐cause mortality (n = 1,286) and self‐reported mobility disability obtained at examination in 1998 to 2000 and in a postal questionnaire 3 to 5 years later in 2003. Results High D‐dimer (top vs lowest tertile: adjusted odds ratio (aOR) = 1.46, 95% confidence interval = 1.02–2.05) and IL‐6 (aOR = 1.43, 95% CI = 1.01–2.02) levels (but not CRP or fibrinogen) were associated with greater incident mobility limitation after adjustment for confounders and prevalent disease status. IL‐6, CRP, fibrinogen, and D‐dimer were significantly associated with total mortality after adjustment for confounders. Only D‐dimer and IL‐6 predicted total mortality independent of each other and the other biomarkers. The adjusted hazard ratio (aHR) was 1.16 (95% CI = 1.10–1.22) for a standard deviation increase in log D‐dimer and 1.10 (95% CI = 1.04–1.18) for a standard deviation increase in log IL‐6. D‐dimer was independently related to vascular and nonvascular mortality, and IL‐6 was independently related to vascular mortality. Risks of mobility limitation and mortality were greatest in those with a combination of high D‐dimer and IL‐6 levels. Conclusion D‐dimer and IL‐6 are associated with risk of mobility limitation and mortality in older men without heart failure. The findings suggest that coagulation leads to functional decline and mortality s that inflammation does not explain.</abstract><cop>Hoboken, NJ</cop><pub>Blackwell Publishing Ltd</pub><pmid>25516032</pmid><doi>10.1111/jgs.13133</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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source MEDLINE; Wiley Online Library All Journals
subjects Aged
Biological and medical sciences
Brief Reports
C-Reactive Protein - metabolism
Cause of Death
Coagulation
D-dimer
England - epidemiology
Enzyme-Linked Immunosorbent Assay
Epidemiology
Fibrin Fibrinogen Degradation Products - metabolism
General aspects
Geriatrics
Humans
inflammation
Inflammation - blood
Interleukin-6 - blood
Male
Medical sciences
Mens health
Middle Aged
Miscellaneous
Mobility Limitation
Mortality
Prospective Studies
Public health. Hygiene
Public health. Hygiene-occupational medicine
Risk Assessment
Surveys and Questionnaires
title Associations Between Fibrin D-Dimer, Markers of Inflammation, Incident Self-Reported Mobility Limitation, and All-Cause Mortality in Older Men
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