Glucose and lipopolysaccharide differentially regulate fibroblast growth factor 21 in healthy male human volunteers – A prospective cross‐over trial
Fibroblast growth factor 21 (FGF21) affects the regulation of metabolism. Additionally, anti‐inflammatory properties are attributed to FGF21, and studies in animals and humans show conflicting results. This study aimed to investigate how FGF21 is affected by glucose and lipopolysaccharide (LPS) in h...
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          | Published in | Journal of cellular and molecular medicine Vol. 26; no. 24; pp. 5998 - 6005 | 
|---|---|
| Main Authors | , , , , , , , , , , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        England
          John Wiley & Sons, Inc
    
        01.12.2022
     John Wiley and Sons Inc  | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 1582-1838 1582-4934 1582-4934  | 
| DOI | 10.1111/jcmm.17614 | 
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| Abstract | Fibroblast growth factor 21 (FGF21) affects the regulation of metabolism. Additionally, anti‐inflammatory properties are attributed to FGF21, and studies in animals and humans show conflicting results. This study aimed to investigate how FGF21 is affected by glucose and lipopolysaccharide (LPS) in humans. Therefore, FGF21 was measured eight times at different time points within 48 h in this prospective cross‐over trial after glucose and LPS on two different study days. The study included ten healthy, non‐smoking male subjects aged 18–40. Repeated measures analysis of variance and paired t‐test as post hoc analysis were applied. The administration of glucose and LPS resulted in a significant difference in regulating FGF21 (p < 0.001). After glucose administration, FGF21 declined sharply at 360 min, with a subsequent steep increase that exceeded baseline levels. LPS induced a drop in FGF21 after 180 min, while the baseline concentrations were not reached. After 180 min and 24 h, a statistically significant difference was demonstrated after adjusting the Bonferroni–Holm method. So, our results support the hypothesis that glucose and LPS differentially affect the human expression of FGF21 over 48 h. | 
    
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| AbstractList | Fibroblast growth factor 21 (FGF21) affects the regulation of metabolism. Additionally, anti-inflammatory properties are attributed to FGF21, and studies in animals and humans show conflicting results. This study aimed to investigate how FGF21 is affected by glucose and lipopolysaccharide (LPS) in humans. Therefore, FGF21 was measured eight times at different time points within 48 h in this prospective cross-over trial after glucose and LPS on two different study days. The study included ten healthy, non-smoking male subjects aged 18-40. Repeated measures analysis of variance and paired t-test as post hoc analysis were applied. The administration of glucose and LPS resulted in a significant difference in regulating FGF21 (p < 0.001). After glucose administration, FGF21 declined sharply at 360 min, with a subsequent steep increase that exceeded baseline levels. LPS induced a drop in FGF21 after 180 min, while the baseline concentrations were not reached. After 180 min and 24 h, a statistically significant difference was demonstrated after adjusting the Bonferroni-Holm method. So, our results support the hypothesis that glucose and LPS differentially affect the human expression of FGF21 over 48 h.Fibroblast growth factor 21 (FGF21) affects the regulation of metabolism. Additionally, anti-inflammatory properties are attributed to FGF21, and studies in animals and humans show conflicting results. This study aimed to investigate how FGF21 is affected by glucose and lipopolysaccharide (LPS) in humans. Therefore, FGF21 was measured eight times at different time points within 48 h in this prospective cross-over trial after glucose and LPS on two different study days. The study included ten healthy, non-smoking male subjects aged 18-40. Repeated measures analysis of variance and paired t-test as post hoc analysis were applied. The administration of glucose and LPS resulted in a significant difference in regulating FGF21 (p < 0.001). After glucose administration, FGF21 declined sharply at 360 min, with a subsequent steep increase that exceeded baseline levels. LPS induced a drop in FGF21 after 180 min, while the baseline concentrations were not reached. After 180 min and 24 h, a statistically significant difference was demonstrated after adjusting the Bonferroni-Holm method. So, our results support the hypothesis that glucose and LPS differentially affect the human expression of FGF21 over 48 h. Fibroblast growth factor 21 (FGF21) affects the regulation of metabolism. Additionally, anti-inflammatory properties are attributed to FGF21, and studies in animals and humans show conflicting results. This study aimed to investigate how FGF21 is affected by glucose and lipopolysaccharide (LPS) in humans. Therefore, FGF21 was measured eight times at different time points within 48 h in this prospective cross-over trial after glucose and LPS on two different study days. The study included ten healthy, non-smoking male subjects aged 18-40. Repeated measures analysis of variance and paired t-test as post hoc analysis were applied. The administration of glucose and LPS resulted in a significant difference in regulating FGF21 (p < 0.001). After glucose administration, FGF21 declined sharply at 360 min, with a subsequent steep increase that exceeded baseline levels. LPS induced a drop in FGF21 after 180 min, while the baseline concentrations were not reached. After 180 min and 24 h, a statistically significant difference was demonstrated after adjusting the Bonferroni-Holm method. So, our results support the hypothesis that glucose and LPS differentially affect the human expression of FGF21 over 48 h. Fibroblast growth factor 21 (FGF21) affects the regulation of metabolism. Additionally, anti‐inflammatory properties are attributed to FGF21, and studies in animals and humans show conflicting results. This study aimed to investigate how FGF21 is affected by glucose and lipopolysaccharide (LPS) in humans. Therefore, FGF21 was measured eight times at different time points within 48 h in this prospective cross‐over trial after glucose and LPS on two different study days. The study included ten healthy, non‐smoking male subjects aged 18–40. Repeated measures analysis of variance and paired t‐test as post hoc analysis were applied. The administration of glucose and LPS resulted in a significant difference in regulating FGF21 (p < 0.001). After glucose administration, FGF21 declined sharply at 360 min, with a subsequent steep increase that exceeded baseline levels. LPS induced a drop in FGF21 after 180 min, while the baseline concentrations were not reached. After 180 min and 24 h, a statistically significant difference was demonstrated after adjusting the Bonferroni–Holm method. So, our results support the hypothesis that glucose and LPS differentially affect the human expression of FGF21 over 48 h. Fibroblast growth factor 21 (FGF21) affects the regulation of metabolism. Additionally, anti‐inflammatory properties are attributed to FGF21, and studies in animals and humans show conflicting results. This study aimed to investigate how FGF21 is affected by glucose and lipopolysaccharide (LPS) in humans. Therefore, FGF21 was measured eight times at different time points within 48 h in this prospective cross‐over trial after glucose and LPS on two different study days. The study included ten healthy, non‐smoking male subjects aged 18–40. Repeated measures analysis of variance and paired t ‐test as post hoc analysis were applied. The administration of glucose and LPS resulted in a significant difference in regulating FGF21 ( p < 0.001). After glucose administration, FGF21 declined sharply at 360 min, with a subsequent steep increase that exceeded baseline levels. LPS induced a drop in FGF21 after 180 min, while the baseline concentrations were not reached. After 180 min and 24 h, a statistically significant difference was demonstrated after adjusting the Bonferroni–Holm method. So, our results support the hypothesis that glucose and LPS differentially affect the human expression of FGF21 over 48 h.  | 
    
| Author | Wagner, Thomas Heinzl, Matthias Wolfgang Klammer, Carmen Feldbauer, Roland Rosenberger, Klemens Dieplinger, Benjamin Obendorf, Florian Resl, Michael Egger‐Salmhofer, Margot Pohlhammer, Johannes Clodi, Martin  | 
    
| AuthorAffiliation | 1 Department of Medicine Konventhospital Barmherzige Brueder Linz (St. John of God Hospital Linz) Linz Austria 3 Department of Internal Medicine Klinikum Rohrbach Rohrbach Austria 2 ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz Linz Austria 4 Department of Laboratory Medicine Konventhospital Barmherzige Brueder Linz and Ordensklinikum Linz Barmherzige Schwestern Linz Austria  | 
    
| AuthorAffiliation_xml | – name: 3 Department of Internal Medicine Klinikum Rohrbach Rohrbach Austria – name: 4 Department of Laboratory Medicine Konventhospital Barmherzige Brueder Linz and Ordensklinikum Linz Barmherzige Schwestern Linz Austria – name: 1 Department of Medicine Konventhospital Barmherzige Brueder Linz (St. John of God Hospital Linz) Linz Austria – name: 2 ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz Linz Austria  | 
    
| Author_xml | – sequence: 1 givenname: Johannes orcidid: 0000-0001-7477-9019 surname: Pohlhammer fullname: Pohlhammer, Johannes organization: ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz – sequence: 2 givenname: Matthias Wolfgang surname: Heinzl fullname: Heinzl, Matthias Wolfgang organization: ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz – sequence: 3 givenname: Carmen surname: Klammer fullname: Klammer, Carmen organization: ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz – sequence: 4 givenname: Roland surname: Feldbauer fullname: Feldbauer, Roland organization: ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz – sequence: 5 givenname: Klemens surname: Rosenberger fullname: Rosenberger, Klemens organization: Klinikum Rohrbach – sequence: 6 givenname: Michael surname: Resl fullname: Resl, Michael organization: ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz – sequence: 7 givenname: Thomas surname: Wagner fullname: Wagner, Thomas organization: ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz – sequence: 8 givenname: Florian surname: Obendorf fullname: Obendorf, Florian organization: ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz – sequence: 9 givenname: Margot surname: Egger‐Salmhofer fullname: Egger‐Salmhofer, Margot organization: Konventhospital Barmherzige Brueder Linz and Ordensklinikum Linz Barmherzige Schwestern – sequence: 10 givenname: Benjamin surname: Dieplinger fullname: Dieplinger, Benjamin organization: Konventhospital Barmherzige Brueder Linz and Ordensklinikum Linz Barmherzige Schwestern – sequence: 11 givenname: Martin surname: Clodi fullname: Clodi, Martin email: martin.clodi@bblinz.at organization: ICMR–Institute for Cardiovascular and Metabolic Research, JKU Linz  | 
    
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36415151$$D View this record in MEDLINE/PubMed | 
    
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| Copyright | 2022 The Authors. published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. 2022 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the "License"). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.  | 
    
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| SubjectTerms | Adenosine Apoptosis Blood pressure Body fat Creatinine Cross-Over Studies Cytokines Deoxyribonucleic acid DNA Electrocardiography fibroblast growth factor 21 Fibroblast growth factors Fibroblast Growth Factors - metabolism Fibroblasts Glucose Growth factors Healthy Volunteers human endotoxin model Humans Hyperglycemia Inflammation lipopolysaccharide Lipopolysaccharides Lipopolysaccharides - pharmacology Liver Male Metabolism Original Oxidative stress Peptides Prospective Studies Protein expression Proteins Statistical analysis Variance analysis  | 
    
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| Title | Glucose and lipopolysaccharide differentially regulate fibroblast growth factor 21 in healthy male human volunteers – A prospective cross‐over trial | 
    
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