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Serum Galectin-3 and Subsequent Risk of Coronary Heart Disease in Subjects With Childhood-Onset Type 1 Diabetes: A Cohort Study.
Saeed, Maryam; Tapia, German; Ariansen, Inger; Stene, Lars C; Seljeflot, Ingebjørg; Tell, Grethe S; Skrivarhaug, Torild; Joner, Geir.
Affiliation
  • Saeed M; Division of Pediatric and Adolescent Medicine, Oslo University Hospital, Oslo, Norway maryam.saeed@medisin.uio.no.
  • Tapia G; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Ariansen I; Department of Chronic Diseases and Ageing, Norwegian Institute of Public Health, Oslo, Norway.
  • Stene LC; Department of Chronic Diseases and Ageing, Norwegian Institute of Public Health, Oslo, Norway.
  • Seljeflot I; Department of Chronic Diseases and Ageing, Norwegian Institute of Public Health, Oslo, Norway.
  • Tell GS; Institute of Clinical Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Skrivarhaug T; Department of Cardiology, Center for Clinical Heart Research, Oslo University Hospital, Oslo, Norway.
  • Joner G; Department of Chronic Diseases and Ageing, Norwegian Institute of Public Health, Oslo, Norway.
Diabetes Care ; 44(3): 810-816, 2021 03.
Article in En | MEDLINE | ID: mdl-33408220
ABSTRACT

OBJECTIVE:

To study whether serum galectin-3 and other biomarkers of inflammation predict coronary heart disease (CHD) in subjects with long-standing childhood-onset type 1 diabetes. RESEARCH DESIGN AND

METHODS:

A population-based nationwide cohort of 299 subjects with type 1 diabetes diagnosed in Norway at <15 years of age during 1973-1982 was examined in 2002-2003 at a mean age of 33 years (range 21-44), with mean diabetes duration of 24 years (range 19-30). Subjects were followed through 31 December 2017 for their first CHD event registered by a hospitalization or cause of death using nationwide registries. Stored serum samples were available for 296 subjects and analyzed for interleukin-6 (IL-6), IL-6 receptor, IL-18, hs-CRP, matrix metalloproteinase-9, tissue inhibitor of metalloproteinase-1 (TIMP-1), galectin-3, and high-sensitivity troponin T. Adjusted hazard ratios (aHRs) for CHD per SD increase in biomarker were estimated using Cox regression.

RESULTS:

Of 295 subjects, 40 (13.6%) had a documented CHD event during a mean follow-up of 14.4 years (range 0.5-16). IL-6 (aHR 1.32 [95% CI 1.07-1.63]), galectin-3 (aHR 1.44 [95% CI 1.09-1.80]), and TIMP-1 (aHR 1.37 [95% CI 1.04-1.81]) were significant predictors of CHD after adjustment for conventional risk factors.

CONCLUSIONS:

Galectin-3 was significantly associated with future CHD in subjects with type 1 diabetes, and if the results are replicated in larger studies, it may aid in prediction together with conventional risk factors for CHD.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Coronary Disease / Diabetes Mellitus, Type 1 Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Child / Humans Language: En Journal: Diabetes Care Year: 2021 Type: Article Affiliation country: Norway

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Coronary Disease / Diabetes Mellitus, Type 1 Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Child / Humans Language: En Journal: Diabetes Care Year: 2021 Type: Article Affiliation country: Norway