{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,16]],"date-time":"2026-09-16T14:54:22Z","timestamp":1789570462292,"version":"build-2803163510"},"reference-count":30,"publisher":"Wiley","issue":"12","license":[{"start":{"date-parts":[[2014,12,17]],"date-time":"2014-12-17T00:00:00Z","timestamp":1418774400000},"content-version":"vor","delay-in-days":16,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc\/4.0\/"}],"funder":[{"DOI":"10.13039\/501100000274","name":"British Heart Foundation","doi-asserted-by":"publisher","award":["RG\/08\/013\/25942"],"award-info":[{"award-number":["RG\/08\/013\/25942"]}],"id":[{"id":"10.13039\/501100000274","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J American Geriatrics Society"],"published-print":{"date-parts":[[2014,12]]},"abstract":"<jats:sec>\n                    <jats:title>Objectives<\/jats:title>\n                    <jats:p>\n                      To examine the independent relationships between fibrin\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      \u2010dimer, interleukin 6 (\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20106),\n                      <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>\n                      \u2010reactive protein (\n                      <jats:styled-content style=\"fixed-case\">CRP<\/jats:styled-content>\n                      ), and fibrinogen and incident mobility limitation and mortality.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Design<\/jats:title>\n                    <jats:p>Prospective.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Setting<\/jats:title>\n                    <jats:p>\n                      General practice in 24\n                      <jats:styled-content style=\"fixed-case\">B<\/jats:styled-content>\n                      ritish towns.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Participants<\/jats:title>\n                    <jats:p>Men aged 60 to 79 without prevalent heart failure followed up for an average of 11.5\u00a0years (N\u00a0=\u00a03,925).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Measurements<\/jats:title>\n                    <jats:p>All\u2010cause mortality (n\u00a0=\u00a01,286) and self\u2010reported mobility disability obtained at examination in 1998 to 2000 and in a postal questionnaire 3 to 5\u00a0years later in 2003.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      High\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      \u2010dimer (top vs lowest tertile: adjusted odds ratio (\n                      <jats:styled-content style=\"fixed-case\">aOR<\/jats:styled-content>\n                      )\u00a0=\u00a01.46, 95% confidence interval\u00a0=\u00a01.02\u20132.05) and\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20106 (a\n                      <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n                      \u00a0=\u00a01.43, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.01\u20132.02) levels (but not\n                      <jats:styled-content style=\"fixed-case\">CRP<\/jats:styled-content>\n                      or fibrinogen) were associated with greater incident mobility limitation after adjustment for confounders and prevalent disease status. IL\u20106,\n                      <jats:styled-content style=\"fixed-case\">CRP<\/jats:styled-content>\n                      , fibrinogen, and\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      \u2010dimer were significantly associated with total mortality after adjustment for confounders. Only\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      \u2010dimer and\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20106 predicted total mortality independent of each other and the other biomarkers. The adjusted hazard ratio (\n                      <jats:styled-content style=\"fixed-case\">aHR<\/jats:styled-content>\n                      ) was 1.16 (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.10\u20131.22) for a standard deviation increase in log\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      \u2010dimer and 1.10 (95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.04\u20131.18) for a standard deviation increase in log\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20106.\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      \u2010dimer was independently related to vascular and nonvascular mortality, and\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20106 was independently related to vascular mortality. Risks of mobility limitation and mortality were greatest in those with a combination of high\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      \u2010dimer and\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20106 levels.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>\n                      <jats:styled-content style=\"fixed-case\">D<\/jats:styled-content>\n                      \u2010dimer and\n                      <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\n                      \u20106 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.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jgs.13133","type":"journal-article","created":{"date-parts":[[2014,12,23]],"date-time":"2014-12-23T06:15:30Z","timestamp":1419315330000},"page":"2357-2362","source":"Crossref","is-referenced-by-count":43,"title":["Associations Between Fibrin\n                    <scp>D<\/scp>\n                    \u2010Dimer, Markers of Inflammation, Incident Self\u2010Reported Mobility Limitation, and All\u2010Cause Mortality in Older Men"],"prefix":"10.1111","volume":"62","author":[{"given":"S. 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