FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2108993389> ?p ?o ?g. }

• W2108993389 endingPage "560" @default.
• W2108993389 startingPage "556" @default.
• W2108993389 abstract "High-density lipoprotein cholesterol (HDL-C), apolipoprotein (apo) A-I, and apo A-II levels were measured in 1,219 normal subjects with no clinical evidence of coronary artery disease, 81 subjects without diabetes but with “significant” coronary artery disease determined by coronary arteriography, and 151 subjects with non-insulin-dependent diabetes mellitus (48 with clinical coronary artery disease and 103 without such disease). In the normal subjects, apo A-II levels were less influenced by age, gender, and use of medications than were apo A-I or HDL-C levels. HDL-C, apo A-I, and apo A-II levels were significantly lower in subjects who had coronary artery disease with or without diabetes than in control subjects. After adjustments were made for age and sex, however, apo A-II levels were no longer significantly different between subjects with diabetes who had and those who did not have coronary artery disease. In subjects without diabetes, apo A-II may provide some advantages over apo A-I and HDL-C in the assessment of risk of coronary artery disease because it is influenced less by age, gender, and medications. In subjects with diabetes, however, apo A-II levels are similar in the presence or absence of coronary artery disease. High-density lipoprotein cholesterol (HDL-C), apolipoprotein (apo) A-I, and apo A-II levels were measured in 1,219 normal subjects with no clinical evidence of coronary artery disease, 81 subjects without diabetes but with “significant” coronary artery disease determined by coronary arteriography, and 151 subjects with non-insulin-dependent diabetes mellitus (48 with clinical coronary artery disease and 103 without such disease). In the normal subjects, apo A-II levels were less influenced by age, gender, and use of medications than were apo A-I or HDL-C levels. HDL-C, apo A-I, and apo A-II levels were significantly lower in subjects who had coronary artery disease with or without diabetes than in control subjects. After adjustments were made for age and sex, however, apo A-II levels were no longer significantly different between subjects with diabetes who had and those who did not have coronary artery disease. In subjects without diabetes, apo A-II may provide some advantages over apo A-I and HDL-C in the assessment of risk of coronary artery disease because it is influenced less by age, gender, and medications. In subjects with diabetes, however, apo A-II levels are similar in the presence or absence of coronary artery disease." @default.
• W2108993389 created "2016-06-24" @default.
• W2108993389 creator A5009659802 @default.
• W2108993389 creator A5019801192 @default.
• W2108993389 creator A5054542042 @default.
• W2108993389 creator A5085960884 @default.
• W2108993389 date "1993-06-01" @default.
• W2108993389 modified "2023-10-15" @default.
• W2108993389 title "Apolipoprotein A-II Levels and Coronary Artery Disease in Subjects With and Without Diabetes: A Study With Use of a Specific Radioimmunoassay for Apolipoprotein A-II" @default.
• W2108993389 cites W1625660792 @default.
• W2108993389 cites W190238394 @default.
• W2108993389 cites W1907754268 @default.
• W2108993389 cites W1908293130 @default.
• W2108993389 cites W1966594148 @default.
• W2108993389 cites W2000095989 @default.
• W2108993389 cites W2012622719 @default.
• W2108993389 cites W2016038813 @default.
• W2108993389 cites W2023070904 @default.
• W2108993389 cites W2034278018 @default.
• W2108993389 cites W2043248515 @default.
• W2108993389 cites W2044046646 @default.
• W2108993389 cites W2044265685 @default.
• W2108993389 cites W2046133282 @default.
• W2108993389 cites W2066597748 @default.
• W2108993389 cites W2079150627 @default.
• W2108993389 cites W2083058051 @default.
• W2108993389 cites W2089261297 @default.
• W2108993389 cites W2092755363 @default.
• W2108993389 cites W2092986019 @default.
• W2108993389 cites W2094768566 @default.
• W2108993389 cites W2109607631 @default.
• W2108993389 cites W2119026555 @default.
• W2108993389 cites W2139667536 @default.
• W2108993389 cites W2161880817 @default.
• W2108993389 cites W2163710824 @default.
• W2108993389 cites W2172031005 @default.
• W2108993389 cites W2336559915 @default.
• W2108993389 cites W2337032743 @default.
• W2108993389 cites W2337433739 @default.
• W2108993389 cites W4243841175 @default.
• W2108993389 doi "https://doi.org/10.1016/s0025-6196(12)60369-3" @default.
• W2108993389 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/8098786" @default.
• W2108993389 hasPublicationYear "1993" @default.
• W2108993389 type Work @default.
• W2108993389 sameAs 2108993389 @default.
• W2108993389 citedByCount "5" @default.
• W2108993389 countsByYear W21089933892019 @default.
• W2108993389 crossrefType "journal-article" @default.
• W2108993389 hasAuthorship W2108993389A5009659802 @default.
• W2108993389 hasAuthorship W2108993389A5019801192 @default.
• W2108993389 hasAuthorship W2108993389A5054542042 @default.
• W2108993389 hasAuthorship W2108993389A5085960884 @default.
• W2108993389 hasConcept C126322002 @default.
• W2108993389 hasConcept C134018914 @default.
• W2108993389 hasConcept C164705383 @default.
• W2108993389 hasConcept C2777466421 @default.
• W2108993389 hasConcept C2778163477 @default.
• W2108993389 hasConcept C2778213512 @default.
• W2108993389 hasConcept C2780072125 @default.
• W2108993389 hasConcept C2780541478 @default.
• W2108993389 hasConcept C555293320 @default.
• W2108993389 hasConcept C62746215 @default.
• W2108993389 hasConcept C71924100 @default.
• W2108993389 hasConceptScore W2108993389C126322002 @default.
• W2108993389 hasConceptScore W2108993389C134018914 @default.
• W2108993389 hasConceptScore W2108993389C164705383 @default.
• W2108993389 hasConceptScore W2108993389C2777466421 @default.
• W2108993389 hasConceptScore W2108993389C2778163477 @default.
• W2108993389 hasConceptScore W2108993389C2778213512 @default.
• W2108993389 hasConceptScore W2108993389C2780072125 @default.
• W2108993389 hasConceptScore W2108993389C2780541478 @default.
• W2108993389 hasConceptScore W2108993389C555293320 @default.
• W2108993389 hasConceptScore W2108993389C62746215 @default.
• W2108993389 hasConceptScore W2108993389C71924100 @default.
• W2108993389 hasIssue "6" @default.
• W2108993389 hasLocation W21089933891 @default.
• W2108993389 hasLocation W21089933892 @default.
• W2108993389 hasOpenAccess W2108993389 @default.
• W2108993389 hasPrimaryLocation W21089933891 @default.
• W2108993389 hasRelatedWork W123759218 @default.
• W2108993389 hasRelatedWork W1973399704 @default.
• W2108993389 hasRelatedWork W1980266135 @default.
• W2108993389 hasRelatedWork W2017524567 @default.
• W2108993389 hasRelatedWork W2074076855 @default.
• W2108993389 hasRelatedWork W2084628138 @default.
• W2108993389 hasRelatedWork W2085228415 @default.
• W2108993389 hasRelatedWork W2570447 @default.
• W2108993389 hasRelatedWork W2901608492 @default.
• W2108993389 hasRelatedWork W4253281463 @default.
• W2108993389 hasVolume "68" @default.
• W2108993389 isParatext "false" @default.
• W2108993389 isRetracted "false" @default.
• W2108993389 magId "2108993389" @default.
• W2108993389 workType "article" @default.