{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,10]],"date-time":"2026-09-10T00:47:34Z","timestamp":1789001254939,"version":"build-2803163510"},"reference-count":29,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"7","content-domain":{"domain":["www.ahajournals.org"],"crossmark-restriction":true},"short-container-title":["JAHA"],"published-print":{"date-parts":[[2019,4,2]]},"abstract":"<jats:sec xml:lang=\"en\">\n            <jats:title>Background<\/jats:title>\n            <jats:p xml:lang=\"en\">Vascular risk factors have been associated with differences in cognitive performance in epidemiological studies, but evidence in patients with coronary heart disease is more limited.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Methods and Results<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              The Montreal Cognitive Assessment score obtained 3.2\u00b10.37\u00a0years after randomization to darapladib, a reversible inhibitor of lipoprotein phospholipase A\n              <jats:sub>2<\/jats:sub>\n              or placebo was evaluated for 10\u00a0634 patients with coronary heart disease from 38 countries in the STABILITY (Stabilization of Atherosclerotic Plaque by Initiation of Darapladib Therapy) trial. The Montreal Cognitive Assessment scores for darapladib and placebo groups were similar (mean\u00b1\n              <jats:styled-content style=\"fixed-case\">SD<\/jats:styled-content>\n              , 25.3\u00b13.84 versus 25.4\u00b13.73, respectively;\n              <jats:italic>P<\/jats:italic>\n              =0.27) and the adjusted odds ratio (\n              <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n              ) for mild cognitive impairment (Montreal Cognitive Assessment score &lt;26) was 1.00 (95%\n              <jats:styled-content style=\"fixed-case\">CI<\/jats:styled-content>\n              , 0.93\u20131.09). Mild cognitive impairment was more likely with increasing age (\n              <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n              , 1.33 [1.27\u20131.41], +5\u00a0years after 65). For other baseline clinical characteristics, the strongest independent predictors of cognitive impairment were education (\u22648\u00a0years versus college\/university,\n              <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n              , 2.95 [2.60\u20133.35]; &gt;8\u00a0years\/trade school versus college\/university,\n              <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n              , 1.38 [1.25\u20131.52] and geographic grouping). Cardiovascular risk factors independently associated with cognitive impairment were history of stroke (\n              <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n              , 1.43 [1.20\u20131.71]); &lt;2.5\u00a0hours of moderate or vigorous intensity exercise\/week (\n              <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n              , 1.19 [1.04\u20131.37]); high\u2010density lipoprotein cholesterol &lt;1.16\u00a0mmol\/L (\n              <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n              , 1.19 [1.04\u20131.37]); diabetes mellitus requiring treatment (\n              <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n              , yes versus no: 1.15 [1.05\u20131.26]); and history of hypertension (\n              <jats:styled-content style=\"fixed-case\">OR<\/jats:styled-content>\n              , 1.12 [1.02\u20131.23]).\n            <\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Conclusions<\/jats:title>\n            <jats:p xml:lang=\"en\">In patients with stable coronary heart disease, cognitive performance was associated with modifiable cardiovascular risk factors, educational level, and global region, but was not influenced by darapladib.<\/jats:p>\n          <\/jats:sec>\n          <jats:sec xml:lang=\"en\">\n            <jats:title>Clinical Trial Registration<\/jats:title>\n            <jats:p xml:lang=\"en\">\n              <jats:styled-content style=\"fixed-case\">URL<\/jats:styled-content>\n              :\n              <jats:ext-link xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" ext-link-type=\"uri\" xlink:href=\"http:\/\/www.clinicaltrials.gov\">http:\/\/www.clinicaltrials.gov<\/jats:ext-link>\n              . Unique identifier:\n              <jats:styled-content style=\"fixed-case\">NCT<\/jats:styled-content>\n              00799903.\n            <\/jats:p>\n          <\/jats:sec>","DOI":"10.1161\/jaha.118.010641","type":"journal-article","created":{"date-parts":[[2019,3,22]],"date-time":"2019-03-22T09:00:30Z","timestamp":1553245230000},"update-policy":"https:\/\/doi.org\/10.1161\/crossmarkpolicy","source":"Crossref","is-referenced-by-count":40,"title":["Cardiovascular and Lifestyle Risk Factors and Cognitive Function in Patients With Stable Coronary Heart Disease"],"prefix":"10.1161","volume":"8","author":[{"given":"Ralph A. 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