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  1. Article ; Online: Hypomagnesemia and Cardiovascular Risk in Type 2 Diabetes.

    Oost, Lynette J / Tack, Cees J / de Baaij, Jeroen H F

    Endocrine reviews

    2022  Volume 44, Issue 3, Page(s) 357–378

    Abstract: Hypomagnesemia is 10-fold more common in individuals with type 2 diabetes (T2D) than in the healthy population. Factors that are involved in this high prevalence are low Mg2+ intake, gut microbiome composition, medication use, and presumably genetics. ... ...

    Abstract Hypomagnesemia is 10-fold more common in individuals with type 2 diabetes (T2D) than in the healthy population. Factors that are involved in this high prevalence are low Mg2+ intake, gut microbiome composition, medication use, and presumably genetics. Hypomagnesemia is associated with insulin resistance, which subsequently increases the risk to develop T2D or deteriorates glycemic control in existing diabetes. Mg2+ supplementation decreases T2D-associated features like dyslipidemia and inflammation, which are important risk factors for cardiovascular disease (CVD). Epidemiological studies have shown an inverse association between serum Mg2+ and the risk of developing heart failure (HF), atrial fibrillation (AF), and microvascular disease in T2D. The potential protective effect of Mg2+ on HF and AF may be explained by reduced oxidative stress, fibrosis, and electrical remodeling in the heart. In microvascular disease, Mg2+ reduces the detrimental effects of hyperglycemia and improves endothelial dysfunction; however, clinical studies assessing the effect of long-term Mg2+ supplementation on CVD incidents are lacking, and gaps remain on how Mg2+ may reduce CVD risk in T2D. Despite the high prevalence of hypomagnesemia in people with T2D, routine screening of Mg2+ deficiency to provide Mg2+ supplementation when needed is not implemented in clinical care as sufficient clinical evidence is lacking. In conclusion, hypomagnesemia is common in people with T2D and is involved both as cause, probably through molecular mechanisms leading to insulin resistance, and as consequence and is prospectively associated with development of HF, AF, and microvascular complications. Whether long-term supplementation of Mg2+ is beneficial, however, remains to be determined.
    MeSH term(s) Humans ; Diabetes Mellitus, Type 2/complications ; Diabetes Mellitus, Type 2/drug therapy ; Risk Factors ; Cardiovascular Diseases/etiology ; Cardiovascular Diseases/complications ; Magnesium/therapeutic use ; Insulin Resistance ; Heart Disease Risk Factors
    Chemical Substances Magnesium (I38ZP9992A)
    Language English
    Publishing date 2022-11-08
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 603096-8
    ISSN 1945-7189 ; 0163-769X
    ISSN (online) 1945-7189
    ISSN 0163-769X
    DOI 10.1210/endrev/bnac028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: The association between hypomagnesemia and poor glycaemic control in type 1 diabetes is limited to insulin resistant individuals.

    Oost, Lynette J / van Heck, Julia I P / Tack, Cees J / de Baaij, Jeroen H F

    Scientific reports

    2022  Volume 12, Issue 1, Page(s) 6433

    Abstract: In a cohort of adults with type 1 diabetes, we examined the prevalence of hypomagnesemia and the correlation of serum magnesium levels with metabolic determinants, such as glycaemic control (as ... ...

    Abstract In a cohort of adults with type 1 diabetes, we examined the prevalence of hypomagnesemia and the correlation of serum magnesium levels with metabolic determinants, such as glycaemic control (as HbA
    MeSH term(s) Adult ; Aged ; Biomarkers ; Blood Glucose/metabolism ; C-Reactive Protein ; Cytokines ; Diabetes Mellitus, Type 1/complications ; Diabetes Mellitus, Type 1/drug therapy ; Diabetes Mellitus, Type 2/complications ; Glycemic Control ; Humans ; Hyperglycemia/complications ; Insulin ; Insulin Resistance ; Magnesium
    Chemical Substances Biomarkers ; Blood Glucose ; Cytokines ; Insulin ; C-Reactive Protein (9007-41-4) ; Magnesium (I38ZP9992A)
    Language English
    Publishing date 2022-04-19
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/s41598-022-10436-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Genome-wide association study of serum magnesium in type 2 diabetes.

    Oost, Lynette J / Slieker, Roderick C / Blom, Marieke T / 't Hart, Leen M / Hoenderop, Joost G J / Beulens, Joline W J / de Baaij, Jeroen H F

    Genes & nutrition

    2024  Volume 19, Issue 1, Page(s) 2

    Abstract: People with type 2 diabetes have a tenfold higher prevalence of hypomagnesemia, which is suggested to be caused by low dietary magnesium intake, medication use, and genetics. This study aims to identify the genetic loci that influence serum magnesium ... ...

    Abstract People with type 2 diabetes have a tenfold higher prevalence of hypomagnesemia, which is suggested to be caused by low dietary magnesium intake, medication use, and genetics. This study aims to identify the genetic loci that influence serum magnesium concentration in 3466 people with type 2 diabetes. The GWAS models were adjusted for age, sex, eGFR, and HbA1c. Associated traits were identified using publicly available data from GTEx consortium, a human kidney eQTL atlas, and the Open GWAS database. The GWAS identified a genome-wide significant locus in TAF3 (p = 2.9 × 10
    Language English
    Publishing date 2024-01-26
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 2416599-2
    ISSN 1865-3499 ; 1555-8932
    ISSN (online) 1865-3499
    ISSN 1555-8932
    DOI 10.1186/s12263-024-00738-5
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The authors reply: Letter on: "Fibroblast growth factor 21 controls mitophagy and muscle mass" by Oost et al.

    Oost, Lynette J / Sandri, Marco / Romanello, Vanina

    Journal of cachexia, sarcopenia and muscle

    2019  Volume 11, Issue 1, Page(s) 338–340

    MeSH term(s) Fibroblast Growth Factors ; Humans ; Mitophagy ; Muscular Diseases
    Chemical Substances fibroblast growth factor 21 ; Fibroblast Growth Factors (62031-54-3)
    Language English
    Publishing date 2019-11-06
    Publishing country Germany
    Document type Letter ; Comment
    ZDB-ID 2586864-0
    ISSN 2190-6009 ; 2190-5991
    ISSN (online) 2190-6009
    ISSN 2190-5991
    DOI 10.1002/jcsm.12500
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Magnesium increases insulin-dependent glucose uptake in adipocytes.

    Oost, Lynette J / Kurstjens, Steef / Ma, Chao / Hoenderop, Joost G J / Tack, Cees J / de Baaij, Jeroen H F

    Frontiers in endocrinology

    2022  Volume 13, Page(s) 986616

    Abstract: Background: Type 2 diabetes (T2D) is characterized by a decreased insulin sensitivity. Magnesium (Mg: Methods: First, the association of low plasma Mg: Results: In people with T2D, plasma Mg: Conclusions: ... ...

    Abstract Background: Type 2 diabetes (T2D) is characterized by a decreased insulin sensitivity. Magnesium (Mg
    Methods: First, the association of low plasma Mg
    Results: In people with T2D, plasma Mg
    Conclusions: Mg
    MeSH term(s) Adipocytes/metabolism ; Diabetes Mellitus, Type 2/metabolism ; Glucose/metabolism ; Humans ; Insulin/metabolism ; Insulin/pharmacology ; Insulin Resistance ; Magnesium ; Proto-Oncogene Proteins c-akt/metabolism ; Receptor, Insulin/metabolism
    Chemical Substances Insulin ; Receptor, Insulin (EC 2.7.10.1) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1) ; Magnesium (I38ZP9992A) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2022-08-25
    Publishing country Switzerland
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2592084-4
    ISSN 1664-2392
    ISSN 1664-2392
    DOI 10.3389/fendo.2022.986616
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Angiopoietin-like 4 promotes the intracellular cleavage of lipoprotein lipase by PCSK3/furin in adipocytes.

    Dijk, Wieneke / Ruppert, Philip M M / Oost, Lynette J / Kersten, Sander

    The Journal of biological chemistry

    2018  Volume 293, Issue 36, Page(s) 14134–14145

    Abstract: Lipoprotein lipase (LPL) catalyzes the breakdown of circulating triglycerides in muscle and fat. LPL is inhibited by several proteins, including angiopoietin-like 4 (ANGPTL4), and may be cleaved by members of the proprotein convertase subtilisin/kexin ( ... ...

    Abstract Lipoprotein lipase (LPL) catalyzes the breakdown of circulating triglycerides in muscle and fat. LPL is inhibited by several proteins, including angiopoietin-like 4 (ANGPTL4), and may be cleaved by members of the proprotein convertase subtilisin/kexin (PCSK) family. Here, we aimed to investigate the cleavage of LPL in adipocytes by PCSKs and study the potential involvement of ANGPTL4. A substantial portion of LPL in mouse and human adipose tissue was cleaved into N- and C-terminal fragments. Treatment of different adipocytes with the PCSK inhibitor decanoyl-RVKR-chloromethyl ketone markedly decreased LPL cleavage, indicating that LPL is cleaved by PCSKs. Silencing of
    MeSH term(s) 3T3-L1 Cells ; Adipocytes/metabolism ; Angiopoietin-like 4 Protein/physiology ; Animals ; Furin/metabolism ; Humans ; Insulin/pharmacology ; Lipoprotein Lipase/metabolism ; Mice
    Chemical Substances Angiopoietin-like 4 Protein ; Insulin ; Lipoprotein Lipase (EC 3.1.1.34) ; Furin (EC 3.4.21.75)
    Language English
    Publishing date 2018-07-18
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2997-x
    ISSN 1083-351X ; 0021-9258
    ISSN (online) 1083-351X
    ISSN 0021-9258
    DOI 10.1074/jbc.RA118.002426
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Fibroblast growth factor 21 controls mitophagy and muscle mass.

    Oost, Lynette J / Kustermann, Monika / Armani, Andrea / Blaauw, Bert / Romanello, Vanina

    Journal of cachexia, sarcopenia and muscle

    2019  Volume 10, Issue 3, Page(s) 630–642

    Abstract: Background: Skeletal muscle is a plastic tissue that adapts to changes in exercise, nutrition, and stress by secreting myokines and myometabolites. These muscle-secreted factors have autocrine, paracrine, and endocrine effects, contributing to whole ... ...

    Abstract Background: Skeletal muscle is a plastic tissue that adapts to changes in exercise, nutrition, and stress by secreting myokines and myometabolites. These muscle-secreted factors have autocrine, paracrine, and endocrine effects, contributing to whole body homeostasis. Muscle dysfunction in aging sarcopenia, cancer cachexia, and diabetes is tightly correlated with the disruption of the physiological homeostasis at the whole body level. The expression levels of the myokine fibroblast growth factor 21 (FGF21) are very low in normal healthy muscles. However, fasting, ER stress, mitochondrial myopathies, and metabolic disorders induce its release from muscles. Although our understanding of the systemic effects of muscle-derived FGF21 is exponentially increasing, the direct contribution of FGF21 to muscle function has not been investigated yet.
    Methods: Muscle-specific FGF21 knockout mice were generated to investigate the consequences of FGF21 deletion concerning skeletal muscle mass and force. To identify the mechanisms underlying FGF21-dependent adaptations in skeletal muscle during starvation, the study was performed on muscles collected from both fed and fasted adult mice. In vivo overexpression of FGF21 was performed in skeletal muscle to assess whether FGF21 is sufficient per se to induce muscle atrophy.
    Results: We show that FGF21 does not contribute to muscle homeostasis in basal conditions in terms of fibre type distribution, fibre size, and muscle force. In contrast, FGF21 is required for fasting-induced muscle atrophy and weakness. The mass of isolated muscles from control-fasted mice was reduced by 15-25% (P < 0.05) compared with fed control mice. FGF21-null muscles, however, were significantly protected from muscle loss and weakness during fasting. Such important protection is due to the maintenance of protein synthesis rate in knockout muscles during fasting compared with a 70% reduction in control-fasted muscles (P < 0.01), together with a significant reduction of the mitophagy flux via the regulation of the mitochondrial protein Bnip3. The contribution of FGF21 to the atrophy programme was supported by in vivo FGF21 overexpression in muscles, which was sufficient to induce autophagy and muscle loss by 15% (P < 0.05). Bnip3 inhibition protected against FGF21-dependent muscle wasting in adult animals (P < 0.05).
    Conclusions: FGF21 is a novel player in the regulation of muscle mass that requires the mitophagy protein Bnip3.
    MeSH term(s) Animals ; Disease Models, Animal ; Fasting/adverse effects ; Fibroblast Growth Factors/genetics ; Fibroblast Growth Factors/metabolism ; Humans ; Membrane Proteins/metabolism ; Mice ; Mice, Knockout ; Mitochondria/metabolism ; Mitochondrial Proteins/metabolism ; Mitophagy ; Muscle, Skeletal/cytology ; Muscle, Skeletal/pathology ; Muscular Atrophy/etiology ; Muscular Atrophy/pathology
    Chemical Substances BNip3 protein, mouse ; Membrane Proteins ; Mitochondrial Proteins ; fibroblast growth factor 21 ; Fibroblast Growth Factors (62031-54-3)
    Language English
    Publishing date 2019-03-20
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2586864-0
    ISSN 2190-6009 ; 2190-5991
    ISSN (online) 2190-6009
    ISSN 2190-5991
    DOI 10.1002/jcsm.12409
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Angiopoietin-like 4 promotes the intracellular cleavage of lipoprotein lipase by PCSK3/furin in adipocytes

    Dijk, Wieneke / Ruppert, Philip M.M. / Oost, Lynette J. / Kersten, Sander

    Journal of Biological Chemistry

    2018  Volume 293, Issue 36

    Abstract: Lipoprotein lipase (LPL) catalyzes the breakdown of circulating triglycerides in muscle and fat. LPL is inhibited by several proteins, including angiopoietin-like 4 (ANGPTL4), and may be cleaved by members of the proprotein convertase subtilisin/ kexin ( ... ...

    Abstract Lipoprotein lipase (LPL) catalyzes the breakdown of circulating triglycerides in muscle and fat. LPL is inhibited by several proteins, including angiopoietin-like 4 (ANGPTL4), and may be cleaved by members of the proprotein convertase subtilisin/ kexin (PCSK) family. Here, we aimed to investigate the cleavage of LPL in adipocytes by PCSKs and study the potential involvement of ANGPTL4. A substantial portion of LPL in mouse and human adipose tissue was cleaved into N- and C-terminal fragments. Treatment of different adipocytes with the PCSK inhibitor decanoyl-RVKR-chloromethyl ketone markedly decreased LPL cleavage, indicating that LPL is cleaved by PCSKs. Silencing of Pcsk3/furin significantly decreased LPL cleavage in cell culture medium and lysates of 3T3-L1 adipocytes. Remarkably, PCSK-mediated cleavage of LPL in adipocytes was diminished by Angptl4 silencing and was decreased in adipocytes and adipose tissue of Angptl4/ mice. Differences in LPL cleavage between Angptl4/ and WT mice were abrogated by treatment with decanoyl-RVKR-chloromethyl ketone. Induction of ANGPTL4 in adipose tissue during fasting enhanced PCSK-mediated LPL cleavage, concurrent with decreased LPL activity, in WT but not Angptl4/ mice. In adipocytes, after removal of cell surface LPL by heparin, levels of N-terminal LPL were still markedly higher in WT compared with Angptl4/ adipocytes, suggesting that stimulation of PCSK-mediated LPL cleavage by ANGPTL4 occurs intracellularly. Finally, treating adipocytes with insulin increased full-length LPL and decreased N-terminal LPL in an ANGPTL4-dependent manner. In conclusion, ANGPTL4 promotes PCSK-mediated intracellular cleavage of LPL in adipocytes, likely contributing to regulation of LPL in adipose tissue. Our data provide further support for an intracellular action of ANGPTL4 in adipocytes.
    Keywords Life Science
    Subject code 610
    Language English
    Publishing country nl
    Document type Article ; Online
    ZDB-ID 2997-x
    ISSN 1083-351X ; 0021-9258
    ISSN (online) 1083-351X
    ISSN 0021-9258
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Serum Magnesium Is Inversely Associated With Heart Failure, Atrial Fibrillation, and Microvascular Complications in Type 2 Diabetes.

    Oost, Lynette J / van der Heijden, Amber A W A / Vermeulen, Emma A / Bos, Caro / Elders, Petra J M / Slieker, Roderick C / Kurstjens, Steef / van Berkel, Miranda / Hoenderop, Joost G J / Tack, Cees J / Beulens, Joline W J / de Baaij, Jeroen H F

    Diabetes care

    2021  Volume 44, Issue 8, Page(s) 1757–1765

    Abstract: Objective: We investigated whether serum magnesium (Mg: Research design and methods: We analyzed in 4,348 participants the association of serum Mg: Results: The average baseline serum Mg: Conclusions: Serum ... ...

    Abstract Objective: We investigated whether serum magnesium (Mg
    Research design and methods: We analyzed in 4,348 participants the association of serum Mg
    Results: The average baseline serum Mg
    Conclusions: Serum Mg
    MeSH term(s) Atrial Fibrillation/complications ; Atrial Fibrillation/epidemiology ; Diabetes Mellitus, Type 2/complications ; Glycated Hemoglobin A ; Heart Failure/epidemiology ; Heart Failure/etiology ; Humans ; Magnesium
    Chemical Substances Glycated Hemoglobin A ; Magnesium (I38ZP9992A)
    Language English
    Publishing date 2021-06-18
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 441231-x
    ISSN 1935-5548 ; 0149-5992
    ISSN (online) 1935-5548
    ISSN 0149-5992
    DOI 10.2337/dc21-0236
    Database MEDical Literature Analysis and Retrieval System OnLINE

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