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Higher hemoglobin levels are an independent risk factor for adverse metabolism and higher mortality in a 20-year follow-up

The aim of this study was to cross-sectionally and longitudinally examine whether higher hemoglobin (Hb) levels within the normal variation associate with key components of metabolic syndrome and total and cardiovascular mortality. The study included 967 Finnish subjects (age 40–59 years) followed f...

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Autores principales: Tapio, Joona, Vähänikkilä, Hannu, Kesäniemi, Y. Antero, Ukkola, Olavi, Koivunen, Peppi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497471/
https://www.ncbi.nlm.nih.gov/pubmed/34620927
http://dx.doi.org/10.1038/s41598-021-99217-9
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author Tapio, Joona
Vähänikkilä, Hannu
Kesäniemi, Y. Antero
Ukkola, Olavi
Koivunen, Peppi
author_facet Tapio, Joona
Vähänikkilä, Hannu
Kesäniemi, Y. Antero
Ukkola, Olavi
Koivunen, Peppi
author_sort Tapio, Joona
collection PubMed
description The aim of this study was to cross-sectionally and longitudinally examine whether higher hemoglobin (Hb) levels within the normal variation associate with key components of metabolic syndrome and total and cardiovascular mortality. The study included 967 Finnish subjects (age 40–59 years) followed for ≥ 20 years. The focus was on Hb levels, cardiovascular diseases (CVDs) and mortality rates. Higher Hb levels associated positively with key anthropometric and metabolic parameters at baseline. At the follow-up similar associations were seen in men. The highest Hb quartile showed higher leptin levels and lower adiponectin levels at baseline and follow-up (p < 0.05) and lower plasma ghrelin levels at baseline (p < 0.05). Higher baseline Hb levels associated independently with prevalence of type 2 diabetes at follow-up (p < 0.01). The highest Hb quartile associated with higher serum alanine aminotransferase levels (p < 0.001) and independently with increased risk for liver fat accumulation (OR 1.63 [1.03; 2.57]) at baseline. The highest Hb quartile showed increased risk for total (HR = 1.48 [1.01; 2.16]) and CVD-related mortality (HR = 2.08 [1.01; 4.29]). Higher Hb levels associated with an adverse metabolic profile, increased prevalence of key components of metabolic syndrome and higher risk for CVD-related and total mortality.
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spelling pubmed-84974712021-10-08 Higher hemoglobin levels are an independent risk factor for adverse metabolism and higher mortality in a 20-year follow-up Tapio, Joona Vähänikkilä, Hannu Kesäniemi, Y. Antero Ukkola, Olavi Koivunen, Peppi Sci Rep Article The aim of this study was to cross-sectionally and longitudinally examine whether higher hemoglobin (Hb) levels within the normal variation associate with key components of metabolic syndrome and total and cardiovascular mortality. The study included 967 Finnish subjects (age 40–59 years) followed for ≥ 20 years. The focus was on Hb levels, cardiovascular diseases (CVDs) and mortality rates. Higher Hb levels associated positively with key anthropometric and metabolic parameters at baseline. At the follow-up similar associations were seen in men. The highest Hb quartile showed higher leptin levels and lower adiponectin levels at baseline and follow-up (p < 0.05) and lower plasma ghrelin levels at baseline (p < 0.05). Higher baseline Hb levels associated independently with prevalence of type 2 diabetes at follow-up (p < 0.01). The highest Hb quartile associated with higher serum alanine aminotransferase levels (p < 0.001) and independently with increased risk for liver fat accumulation (OR 1.63 [1.03; 2.57]) at baseline. The highest Hb quartile showed increased risk for total (HR = 1.48 [1.01; 2.16]) and CVD-related mortality (HR = 2.08 [1.01; 4.29]). Higher Hb levels associated with an adverse metabolic profile, increased prevalence of key components of metabolic syndrome and higher risk for CVD-related and total mortality. Nature Publishing Group UK 2021-10-07 /pmc/articles/PMC8497471/ /pubmed/34620927 http://dx.doi.org/10.1038/s41598-021-99217-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tapio, Joona
Vähänikkilä, Hannu
Kesäniemi, Y. Antero
Ukkola, Olavi
Koivunen, Peppi
Higher hemoglobin levels are an independent risk factor for adverse metabolism and higher mortality in a 20-year follow-up
title Higher hemoglobin levels are an independent risk factor for adverse metabolism and higher mortality in a 20-year follow-up
title_full Higher hemoglobin levels are an independent risk factor for adverse metabolism and higher mortality in a 20-year follow-up
title_fullStr Higher hemoglobin levels are an independent risk factor for adverse metabolism and higher mortality in a 20-year follow-up
title_full_unstemmed Higher hemoglobin levels are an independent risk factor for adverse metabolism and higher mortality in a 20-year follow-up
title_short Higher hemoglobin levels are an independent risk factor for adverse metabolism and higher mortality in a 20-year follow-up
title_sort higher hemoglobin levels are an independent risk factor for adverse metabolism and higher mortality in a 20-year follow-up
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8497471/
https://www.ncbi.nlm.nih.gov/pubmed/34620927
http://dx.doi.org/10.1038/s41598-021-99217-9
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