Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study

Background Creatine kinase (CK) has been associated with insulin resistance and identified as a risk marker of cardiovascular disease largely by its relationship with hypertension and increased body mass index. This study determined whether CK is a predictor of glycated haemoglobin (HbA1C) in a nond...

Full description

Bibliographic Details
Published in:PLOS ONE
Main Author: Bekkelund, Svein Ivar
Format: Article in Journal/Newspaper
Language:English
Published: PLOS 2023
Subjects:
Online Access:https://hdl.handle.net/10037/29839
https://doi.org/10.1371/journal.pone.0281239
id ftunivtroemsoe:oai:munin.uit.no:10037/29839
record_format openpolar
spelling ftunivtroemsoe:oai:munin.uit.no:10037/29839 2023-09-05T13:23:46+02:00 Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study Bekkelund, Svein Ivar 2023-02-02 https://hdl.handle.net/10037/29839 https://doi.org/10.1371/journal.pone.0281239 eng eng PLOS PLOS ONE Bekkelund. Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study. PLOS ONE. 2023;18(2) FRIDAID 2150839 doi:10.1371/journal.pone.0281239 1932-6203 https://hdl.handle.net/10037/29839 Attribution 4.0 International (CC BY 4.0) openAccess Copyright 2023 The Author(s) https://creativecommons.org/licenses/by/4.0 Journal article Tidsskriftartikkel Peer reviewed publishedVersion 2023 ftunivtroemsoe https://doi.org/10.1371/journal.pone.0281239 2023-08-16T23:06:45Z Background Creatine kinase (CK) has been associated with insulin resistance and identified as a risk marker of cardiovascular disease largely by its relationship with hypertension and increased body mass index. This study determined whether CK is a predictor of glycated haemoglobin (HbA1C) in a nondiabetic general population. Methods Associations between CK and the outcome variable HbA1C (%) were performed by variance and multivariate analyses in 11662 nondiabetic subjects defined as HbA1C (%) <6.5 who participated in the population based Tromsø study (Tromsø 6) in Norway. Results Abnormal elevated CK was detected in 543/11662 participants (4.66%). Mean HbA1C (%) in the “high CK” group was 5.62 (SD = 0.33) compared to 5.52 (SD = 0.36) in the “normal CK” group, P <0.001. CK increased significantly and linearly with higher levels of HbA 1C (%) quartiles in women (P <0.001) and non-linearly in men (P <0.001). In a multivariate analysis, CK was independently associated with HbA 1C (%) after adjusting for age, sex, body mass index, blood pressure, glucose, lipids, C-reactive protein, creatinine, alanine transaminase and aspartate aminotransferase. A 1-unit increase in log CK was associated with a 0.17-unit increase in HbA 1C (%). Conclusion These data demonstrate a positive and independent association between CK and glycated haemoglobin in a nondiabetic general population. Article in Journal/Newspaper Tromsø University of Tromsø: Munin Open Research Archive Norway Tromsø PLOS ONE 18 2 e0281239
institution Open Polar
collection University of Tromsø: Munin Open Research Archive
op_collection_id ftunivtroemsoe
language English
description Background Creatine kinase (CK) has been associated with insulin resistance and identified as a risk marker of cardiovascular disease largely by its relationship with hypertension and increased body mass index. This study determined whether CK is a predictor of glycated haemoglobin (HbA1C) in a nondiabetic general population. Methods Associations between CK and the outcome variable HbA1C (%) were performed by variance and multivariate analyses in 11662 nondiabetic subjects defined as HbA1C (%) <6.5 who participated in the population based Tromsø study (Tromsø 6) in Norway. Results Abnormal elevated CK was detected in 543/11662 participants (4.66%). Mean HbA1C (%) in the “high CK” group was 5.62 (SD = 0.33) compared to 5.52 (SD = 0.36) in the “normal CK” group, P <0.001. CK increased significantly and linearly with higher levels of HbA 1C (%) quartiles in women (P <0.001) and non-linearly in men (P <0.001). In a multivariate analysis, CK was independently associated with HbA 1C (%) after adjusting for age, sex, body mass index, blood pressure, glucose, lipids, C-reactive protein, creatinine, alanine transaminase and aspartate aminotransferase. A 1-unit increase in log CK was associated with a 0.17-unit increase in HbA 1C (%). Conclusion These data demonstrate a positive and independent association between CK and glycated haemoglobin in a nondiabetic general population.
format Article in Journal/Newspaper
author Bekkelund, Svein Ivar
spellingShingle Bekkelund, Svein Ivar
Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study
author_facet Bekkelund, Svein Ivar
author_sort Bekkelund, Svein Ivar
title Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study
title_short Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study
title_full Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study
title_fullStr Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study
title_full_unstemmed Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study
title_sort creatine kinase is associated with glycated haemoglobin in a nondiabetic population. the tromsø study
publisher PLOS
publishDate 2023
url https://hdl.handle.net/10037/29839
https://doi.org/10.1371/journal.pone.0281239
geographic Norway
Tromsø
geographic_facet Norway
Tromsø
genre Tromsø
genre_facet Tromsø
op_relation PLOS ONE
Bekkelund. Creatine kinase is associated with glycated haemoglobin in a nondiabetic population. The Tromsø study. PLOS ONE. 2023;18(2)
FRIDAID 2150839
doi:10.1371/journal.pone.0281239
1932-6203
https://hdl.handle.net/10037/29839
op_rights Attribution 4.0 International (CC BY 4.0)
openAccess
Copyright 2023 The Author(s)
https://creativecommons.org/licenses/by/4.0
op_doi https://doi.org/10.1371/journal.pone.0281239
container_title PLOS ONE
container_volume 18
container_issue 2
container_start_page e0281239
_version_ 1776204348711239680