{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,30]],"date-time":"2026-09-30T22:23:30Z","timestamp":1790807010664,"version":"4.1.0"},"reference-count":41,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2021,11,24]],"date-time":"2021-11-24T00:00:00Z","timestamp":1637712000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J Intern Med"],"published-print":{"date-parts":[[2022,3]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:title>Objectives<\/jats:title><jats:p>We studied apolipoprotein C\u2010III (apoC\u2010III) in relation to diabetic kidney disease (DKD), cardiovascular outcomes, and mortality in type 1 diabetes.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>The cohort comprised 3966 participants from the prospective observational Finnish Diabetic Nephropathy Study. Progression of DKD was determined from medical records. A major adverse cardiac event (MACE) was defined as acute myocardial infarction, coronary revascularization, stroke, or cardiovascular mortality through 2017. Cardiovascular and mortality data were retrieved from national registries.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>ApoC\u2010III predicted DKD progression independent of sex, diabetes duration, blood pressure, HbA<jats:sub>1c<\/jats:sub>, smoking, LDL\u2010cholesterol, lipid\u2010lowering medication, DKD category, and remnant cholesterol (hazard ratio [HR] 1.43 [95% confidence interval 1.05\u20131.94], <jats:italic>p<\/jats:italic>\u00a0= 0.02). ApoC\u2010III also predicted the MACE in a multivariable regression analysis; however, it was not independent of remnant cholesterol (HR 1.05 [0.81\u20131.36, <jats:italic>p<\/jats:italic> = 0.71] with remnant cholesterol; 1.30 [1.03\u20131.64, <jats:italic>p<\/jats:italic> = 0.03] without). DKD\u2010specific analyses revealed that the association was driven by individuals with albuminuria, as no link between apoC\u2010III and the outcome was observed in the normal albumin excretion or kidney failure categories. The same was observed for mortality: Individuals with albuminuria had an adjusted HR of 1.49 (1.03\u20132.16, <jats:italic>p<\/jats:italic> = 0.03) for premature death, while no association was found in the other groups. The highest apoC\u2010III quartile displayed a markedly higher risk of MACE and death than the lower quartiles; however, this nonlinear relationship flattened after adjustment.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusions<\/jats:title><jats:p>The impact of apoC\u2010III on MACE risk and mortality is restricted to those with albuminuria among individuals with type 1 diabetes. This study also revealed that apoC\u2010III predicts DKD progression, independent of the initial DKD category.<\/jats:p><\/jats:sec>","DOI":"10.1111\/joim.13412","type":"journal-article","created":{"date-parts":[[2021,11,26]],"date-time":"2021-11-26T08:01:18Z","timestamp":1637913678000},"page":"338-349","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":15,"title":["Apolipoprotein C\u2010III predicts cardiovascular events and mortality in individuals with type 1 diabetes and albuminuria"],"prefix":"10.1111","volume":"291","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-1192-348X","authenticated-orcid":false,"given":"Fanny","family":"Jansson Sigfrids","sequence":"first","affiliation":[{"name":"Folkh\u00e4lsan Institute of Genetics Folkh\u00e4lsan Research Center  Helsinki Finland"},{"name":"Department of Nephrology University of Helsinki and Helsinki University Hospital  Helsinki Finland"},{"name":"Research Program for Clinical 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Finland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3354-7454","authenticated-orcid":false,"given":"Carol M.","family":"Forsblom","sequence":"additional","affiliation":[{"name":"Folkh\u00e4lsan Institute of Genetics Folkh\u00e4lsan Research Center  Helsinki Finland"},{"name":"Department of Nephrology University of Helsinki and Helsinki University Hospital  Helsinki Finland"},{"name":"Research Program for Clinical and Molecular Metabolism Faculty of Medicine, University of Helsinki  Helsinki Finland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3568-9779","authenticated-orcid":false,"given":"Valma","family":"Harjutsalo","sequence":"additional","affiliation":[{"name":"Folkh\u00e4lsan Institute of Genetics Folkh\u00e4lsan Research Center  Helsinki Finland"},{"name":"Department of Nephrology University of Helsinki and Helsinki University Hospital  Helsinki Finland"},{"name":"Research 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