Matches in SemOpenAlex for { <https://semopenalex.org/work/W2899247961> ?p ?o ?g. }
- W2899247961 abstract "Background: Integration of systems-level biomolecular information with electronic health records has led to recent interest in the glycoprotein acetyls (GlycA) biomarker—a serum- or plasma-derived nuclear magnetic resonance spectroscopy signal that represents the abundance of circulating glycated proteins. GlycA predicts risk of diverse outcomes, including cardiovascular disease, type 2 diabetes mellitus, and all-cause mortality; however, the underlying detailed associations of GlycA’s morbidity and mortality risk are currently unknown. Methods: We used 2 population-based cohorts totaling 11 861 adults from the Finnish general population to test for an association with 468 common incident hospitalization and mortality outcomes during an 8-year follow-up. Further, we utilized 900 angiography patients to test for GlycA association with mortality risk and potential utility for mortality risk discrimination during 12-year follow-up. Results: New associations with GlycA and incident alcoholic liver disease, chronic renal failure, glomerular diseases, chronic obstructive pulmonary disease, inflammatory polyarthropathies, and hypertension were uncovered, and known incident disease associations were replicated. GlycA associations for incident disease outcomes were in general not attenuated when adjusting for hsCRP (high-sensitivity C-reactive protein). Among 900 patients referred to angiography, GlycA had hazard ratios of 4.87 (95% CI, 2.45–9.65) and 5.00 (95% CI, 2.38–10.48) for 12-year risk of mortality in the fourth and fifth quintiles by GlycA levels, demonstrating its prognostic potential for identification of high-risk individuals. When modeled together, both hsCRP and GlycA were attenuated but remained significant. Conclusions: GlycA was predictive of myriad incident diseases across many major internal organs and stratified mortality risk in angiography patients. Both GlycA and hsCRP had shared and independent contributions to mortality risk, suggesting chronic inflammation as an etiological factor. GlycA may be useful in improving risk prediction in specific disease settings." @default.
- W2899247961 created "2018-11-09" @default.
- W2899247961 creator A5001600698 @default.
- W2899247961 creator A5022876944 @default.
- W2899247961 creator A5026787409 @default.
- W2899247961 creator A5041918436 @default.
- W2899247961 creator A5045767788 @default.
- W2899247961 creator A5047024112 @default.
- W2899247961 creator A5049268884 @default.
- W2899247961 creator A5051610805 @default.
- W2899247961 creator A5052434301 @default.
- W2899247961 creator A5054656133 @default.
- W2899247961 creator A5065030179 @default.
- W2899247961 creator A5066237154 @default.
- W2899247961 creator A5078073418 @default.
- W2899247961 creator A5079852650 @default.
- W2899247961 creator A5081478760 @default.
- W2899247961 creator A5081986241 @default.
- W2899247961 creator A5085852635 @default.
- W2899247961 date "2018-11-01" @default.
- W2899247961 modified "2023-10-14" @default.
- W2899247961 title "Biomarker Glycoprotein Acetyls Is Associated With the Risk of a Wide Spectrum of Incident Diseases and Stratifies Mortality Risk in Angiography Patients" @default.
- W2899247961 cites W1835396192 @default.
- W2899247961 cites W1988195069 @default.
- W2899247961 cites W2004505189 @default.
- W2899247961 cites W2019859514 @default.
- W2899247961 cites W2020466729 @default.
- W2899247961 cites W2032329963 @default.
- W2899247961 cites W2045199633 @default.
- W2899247961 cites W2048140618 @default.
- W2899247961 cites W2082219610 @default.
- W2899247961 cites W2086337432 @default.
- W2899247961 cites W2104230242 @default.
- W2899247961 cites W2104342488 @default.
- W2899247961 cites W2104465828 @default.
- W2899247961 cites W2108842111 @default.
- W2899247961 cites W2115819915 @default.
- W2899247961 cites W2128335879 @default.
- W2899247961 cites W2133346314 @default.
- W2899247961 cites W2139957955 @default.
- W2899247961 cites W2147063947 @default.
- W2899247961 cites W2162142051 @default.
- W2899247961 cites W2337946759 @default.
- W2899247961 cites W2339419666 @default.
- W2899247961 cites W2381728735 @default.
- W2899247961 cites W2537269837 @default.
- W2899247961 cites W2547405393 @default.
- W2899247961 cites W2556512023 @default.
- W2899247961 cites W2557929069 @default.
- W2899247961 cites W2738033779 @default.
- W2899247961 cites W2748400555 @default.
- W2899247961 cites W2750254726 @default.
- W2899247961 cites W2767172593 @default.
- W2899247961 cites W2795852751 @default.
- W2899247961 doi "https://doi.org/10.1161/circgen.118.002234" @default.
- W2899247961 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30571186" @default.
- W2899247961 hasPublicationYear "2018" @default.
- W2899247961 type Work @default.
- W2899247961 sameAs 2899247961 @default.
- W2899247961 citedByCount "30" @default.
- W2899247961 countsByYear W28992479612019 @default.
- W2899247961 countsByYear W28992479612020 @default.
- W2899247961 countsByYear W28992479612021 @default.
- W2899247961 countsByYear W28992479612022 @default.
- W2899247961 countsByYear W28992479612023 @default.
- W2899247961 crossrefType "journal-article" @default.
- W2899247961 hasAuthorship W2899247961A5001600698 @default.
- W2899247961 hasAuthorship W2899247961A5022876944 @default.
- W2899247961 hasAuthorship W2899247961A5026787409 @default.
- W2899247961 hasAuthorship W2899247961A5041918436 @default.
- W2899247961 hasAuthorship W2899247961A5045767788 @default.
- W2899247961 hasAuthorship W2899247961A5047024112 @default.
- W2899247961 hasAuthorship W2899247961A5049268884 @default.
- W2899247961 hasAuthorship W2899247961A5051610805 @default.
- W2899247961 hasAuthorship W2899247961A5052434301 @default.
- W2899247961 hasAuthorship W2899247961A5054656133 @default.
- W2899247961 hasAuthorship W2899247961A5065030179 @default.
- W2899247961 hasAuthorship W2899247961A5066237154 @default.
- W2899247961 hasAuthorship W2899247961A5078073418 @default.
- W2899247961 hasAuthorship W2899247961A5079852650 @default.
- W2899247961 hasAuthorship W2899247961A5081478760 @default.
- W2899247961 hasAuthorship W2899247961A5081986241 @default.
- W2899247961 hasAuthorship W2899247961A5085852635 @default.
- W2899247961 hasBestOaLocation W28992479611 @default.
- W2899247961 hasConcept C126322002 @default.
- W2899247961 hasConcept C134018914 @default.
- W2899247961 hasConcept C185592680 @default.
- W2899247961 hasConcept C207103383 @default.
- W2899247961 hasConcept C2779134260 @default.
- W2899247961 hasConcept C2781197716 @default.
- W2899247961 hasConcept C2908647359 @default.
- W2899247961 hasConcept C44249647 @default.
- W2899247961 hasConcept C55493867 @default.
- W2899247961 hasConcept C555293320 @default.
- W2899247961 hasConcept C71924100 @default.
- W2899247961 hasConcept C99454951 @default.
- W2899247961 hasConceptScore W2899247961C126322002 @default.
- W2899247961 hasConceptScore W2899247961C134018914 @default.
- W2899247961 hasConceptScore W2899247961C185592680 @default.
- W2899247961 hasConceptScore W2899247961C207103383 @default.