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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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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. |
format | Online Article Text |
id | pubmed-7424824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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