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Vital status was adjudicated from death certificates. Cox proportional hazards models, adjusted for appropriate confounders, were used to estimate mortality hazards ratios.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Prevalence of any\n                      <jats:styled-content style=\"fixed-case\">AMD<\/jats:styled-content>\n                      was 40.5% at baseline, with 441 (36.7%) having early\n                      <jats:styled-content style=\"fixed-case\">AMD<\/jats:styled-content>\n                      and 46 (3.8%) having late\n                      <jats:styled-content style=\"fixed-case\">AMD<\/jats:styled-content>\n                      . Cumulative mortality was 51.6% over 15\u00a0years of follow\u2010up. Overall, there was no significant association between\n                      <jats:styled-content style=\"fixed-case\">AMD<\/jats:styled-content>\n                      presence or severity and all\u2010cause or cause\u2010specific mortality. Because there was a significant interaction between\n                      <jats:styled-content style=\"fixed-case\">AMD<\/jats:styled-content>\n                      and age in predicting mortality (\n                      <jats:italic>P<\/jats:italic>\n                      \u00a0&lt;\u00a0.05 for each mortality type), analyses were stratified according to age group. In women younger than 80, after adjusting for covariates, late\n                      <jats:styled-content style=\"fixed-case\">AMD<\/jats:styled-content>\n                      was associated with cardiovascular disease (\n                      <jats:styled-content style=\"fixed-case\">CVD<\/jats:styled-content>\n                      ) mortality (hazard ratio (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      )\u00a0=\u00a02.61, 95% confidence interval (\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      )\u00a0=\u00a01.05\u20136.46). In women aged 80 and older, early\n                      <jats:styled-content style=\"fixed-case\">AMD<\/jats:styled-content>\n                      was associated with all\u2010cause (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      \u00a0=\u00a01.39, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.11\u20131.75) and non\u2010\n                      <jats:styled-content style=\"fixed-case\">CVD<\/jats:styled-content>\n                      , noncancer (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      \u00a0=\u00a01.45, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.05\u20132.00) mortality. Any\n                      <jats:styled-content style=\"fixed-case\">AMD<\/jats:styled-content>\n                      was associated with all\u2010cause (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      \u00a0=\u00a01.42, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.13\u20131.78) and\n                      <jats:styled-content style=\"fixed-case\">CVD<\/jats:styled-content>\n                      (\n                      <jats:styled-content style=\"fixed-case\">HR<\/jats:styled-content>\n                      \u00a0=\u00a01.45, 95%\n                      <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n                      \u00a0=\u00a01.01\u20132.09) mortality in women aged 80 and older.\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\">AMD<\/jats:styled-content>\n                      is a predictor of poorer survival in women, especially those aged 80 and older. Determination of shared risk factors may identify novel pathways for intervention that may reduce the risk of both conditions.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1111\/jgs.13405","type":"journal-article","created":{"date-parts":[[2015,5,5]],"date-time":"2015-05-05T00:53:04Z","timestamp":1430787184000},"page":"910-917","source":"Crossref","is-referenced-by-count":19,"title":["Age\u2010Related Macular Degeneration and Mortality in Older Women: The Study of Osteoporotic Fractures"],"prefix":"10.1111","volume":"63","author":[{"given":"Kathryn L.","family":"Pedula","sequence":"first","affiliation":[{"name":"Kaiser Permanente Center for Health Research Northwest\/Hawaii Portland Oregon"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anne L.","family":"Coleman","sequence":"additional","affiliation":[{"name":"Department of Ophthalmology Jules Stein Eye Institute David Geffen School of Medicine Los Angeles California"},{"name":"Department 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