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Galectin-1 is inversely associated with type 2 diabetes independently of obesity – A SCAPIS pilot study()

OBJECTIVES: Galectin-1 is a recently discovered adipokine that increases with obesity and increased energy intake in adipose tissue. Our aim was to assess whether serum galectin-1 is associated with type 2 diabetes (T2D) and other parameters of the metabolic syndrome independently of body mass index...

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Autores principales: Fryk, Emanuel, Strindberg, Lena, Lundqvist, Annika, Sandstedt, Mikael, Bergfeldt, Lennart, Mattsson Hultén, Lillemor, Bergström, Göran, Jansson, Per-Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424824/
https://www.ncbi.nlm.nih.gov/pubmed/32812946
http://dx.doi.org/10.1016/j.metop.2019.100017
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author Fryk, Emanuel
Strindberg, Lena
Lundqvist, Annika
Sandstedt, Mikael
Bergfeldt, Lennart
Mattsson Hultén, Lillemor
Bergström, Göran
Jansson, Per-Anders
author_facet Fryk, Emanuel
Strindberg, Lena
Lundqvist, Annika
Sandstedt, Mikael
Bergfeldt, Lennart
Mattsson Hultén, Lillemor
Bergström, Göran
Jansson, Per-Anders
author_sort Fryk, Emanuel
collection PubMed
description OBJECTIVES: Galectin-1 is a recently discovered adipokine that increases with obesity and increased energy intake in adipose tissue. Our aim was to assess whether serum galectin-1 is associated with type 2 diabetes (T2D) and other parameters of the metabolic syndrome independently of body mass index (BMI) in a cohort from the general population. METHODS: In this cross-sectional population-based cohort study from the western part of Sweden, we investigated associations between serum galectin-1, clinical characteristics and inflammatory markers in 989 women and men aged 50–65 years [part of the Swedish CArdioPulmonary bioImage Study (SCAPIS) pilot cohort]. RESULTS: We showed in linear models that serum galectin-1 was independently and: (1) inversely associated with T2D (p < 0.05) and glucose (p < 0.05); and (2) positively associated with age (p < 0.01), sex (p < 0.01), BMI (p < 0.01), insulin (p < 0.01) and C-reactive protein (p < 0.01). Furthermore, galectin-1 demonstrated univariate correlations with triglycerides (r = 0.20, p < 0.01), homeostasis model assessment for insulin resistance (r = 0.24, p < 0.01), tumor necrosis factor-α (r = 0.24, p < 0.01), interleukin-6 (IL-6; r = 0.20, p < 0.01) and HbA1c (r = 0.14, p < 0.01). CONCLUSION: In a cross-sectional study of a middle-aged population, we showed that serum galectin-1 is: (1) inversely associated with T2D independently of BMI; and (2) independently associated with other markers of the metabolic syndrome These results warrant prospective and functional studies on the role of galectin-1 in T2D.
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spelling pubmed-74248242020-08-17 Galectin-1 is inversely associated with type 2 diabetes independently of obesity – A SCAPIS pilot study() Fryk, Emanuel Strindberg, Lena Lundqvist, Annika Sandstedt, Mikael Bergfeldt, Lennart Mattsson Hultén, Lillemor Bergström, Göran Jansson, Per-Anders Metabol Open Original Research Paper OBJECTIVES: Galectin-1 is a recently discovered adipokine that increases with obesity and increased energy intake in adipose tissue. Our aim was to assess whether serum galectin-1 is associated with type 2 diabetes (T2D) and other parameters of the metabolic syndrome independently of body mass index (BMI) in a cohort from the general population. METHODS: In this cross-sectional population-based cohort study from the western part of Sweden, we investigated associations between serum galectin-1, clinical characteristics and inflammatory markers in 989 women and men aged 50–65 years [part of the Swedish CArdioPulmonary bioImage Study (SCAPIS) pilot cohort]. RESULTS: We showed in linear models that serum galectin-1 was independently and: (1) inversely associated with T2D (p < 0.05) and glucose (p < 0.05); and (2) positively associated with age (p < 0.01), sex (p < 0.01), BMI (p < 0.01), insulin (p < 0.01) and C-reactive protein (p < 0.01). Furthermore, galectin-1 demonstrated univariate correlations with triglycerides (r = 0.20, p < 0.01), homeostasis model assessment for insulin resistance (r = 0.24, p < 0.01), tumor necrosis factor-α (r = 0.24, p < 0.01), interleukin-6 (IL-6; r = 0.20, p < 0.01) and HbA1c (r = 0.14, p < 0.01). CONCLUSION: In a cross-sectional study of a middle-aged population, we showed that serum galectin-1 is: (1) inversely associated with T2D independently of BMI; and (2) independently associated with other markers of the metabolic syndrome These results warrant prospective and functional studies on the role of galectin-1 in T2D. Elsevier 2019-09-05 /pmc/articles/PMC7424824/ /pubmed/32812946 http://dx.doi.org/10.1016/j.metop.2019.100017 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Paper
Fryk, Emanuel
Strindberg, Lena
Lundqvist, Annika
Sandstedt, Mikael
Bergfeldt, Lennart
Mattsson Hultén, Lillemor
Bergström, Göran
Jansson, Per-Anders
Galectin-1 is inversely associated with type 2 diabetes independently of obesity – A SCAPIS pilot study()
title Galectin-1 is inversely associated with type 2 diabetes independently of obesity – A SCAPIS pilot study()
title_full Galectin-1 is inversely associated with type 2 diabetes independently of obesity – A SCAPIS pilot study()
title_fullStr Galectin-1 is inversely associated with type 2 diabetes independently of obesity – A SCAPIS pilot study()
title_full_unstemmed Galectin-1 is inversely associated with type 2 diabetes independently of obesity – A SCAPIS pilot study()
title_short Galectin-1 is inversely associated with type 2 diabetes independently of obesity – A SCAPIS pilot study()
title_sort galectin-1 is inversely associated with type 2 diabetes independently of obesity – a scapis pilot study()
topic Original Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424824/
https://www.ncbi.nlm.nih.gov/pubmed/32812946
http://dx.doi.org/10.1016/j.metop.2019.100017
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