Serum fibroblast growth factor 21 and new-onset metabolic syndrome: KoGES-ARIRANG study

Jung Ran Choi, Jang Young Kim, Il Hwan Park, Ji Hye Huh, Ki Woo Kim, Seung Kuy Cha, Kyu Sang Park, Joon Hyung Sohn, Jong Taek Park, Sang Baek Koh

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Purpose: Fibroblast growth factor 21 (FGF21) is a crucial metabolic regulator, with multiple favorable effects on glucose homeo-stasis and lipid metabolism. Since serum FGF21 level has been implicated as a potential marker for the early identification of metabolic syndrome (MetS), we investigated the association between serum FGF21 level and the development of MetS in a population-based prospective study. Materials and Methods: We conducted a prospective study of 221 randomly sampled adults without MetS from a general population-based cohort study who were examined from 2005–2008 (baseline) and from 2008–2011 (follow-up). Baseline serum FGF21 levels were analyzed using enzyme-linked immunosorbent assay. Results: During the average 2.8-year follow-up period, 82 participants (36.6%) developed new-onset MetS. Serum FGF21 levels were significantly higher in patients with new-onset MetS than in those without MetS (209.56±226.80 vs. 110.09±81.10, p<0.01). In multivariate adjusted models, the odds for MetS development were greater in patients with serum FGF21 levels in the highest quartile, compared to those in the lowest quartile (3.84, 95% confidence interval: 1.59–9.28). Conclusion: Serum FGF21 level was an independent predictor for new-onset MetS in a population-based prospective study.

Original languageEnglish
Pages (from-to)287-293
Number of pages7
JournalYonsei medical journal
Volume59
Issue number2
DOIs
Publication statusPublished - 2018 Mar

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Serum
Prospective Studies
Population
fibroblast growth factor 21
Lipid Metabolism
Cohort Studies
Enzyme-Linked Immunosorbent Assay
Confidence Intervals
Glucose

All Science Journal Classification (ASJC) codes

  • Medicine(all)

Cite this

Choi, Jung Ran ; Kim, Jang Young ; Park, Il Hwan ; Huh, Ji Hye ; Kim, Ki Woo ; Cha, Seung Kuy ; Park, Kyu Sang ; Sohn, Joon Hyung ; Park, Jong Taek ; Koh, Sang Baek. / Serum fibroblast growth factor 21 and new-onset metabolic syndrome : KoGES-ARIRANG study. In: Yonsei medical journal. 2018 ; Vol. 59, No. 2. pp. 287-293.
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abstract = "Purpose: Fibroblast growth factor 21 (FGF21) is a crucial metabolic regulator, with multiple favorable effects on glucose homeo-stasis and lipid metabolism. Since serum FGF21 level has been implicated as a potential marker for the early identification of metabolic syndrome (MetS), we investigated the association between serum FGF21 level and the development of MetS in a population-based prospective study. Materials and Methods: We conducted a prospective study of 221 randomly sampled adults without MetS from a general population-based cohort study who were examined from 2005–2008 (baseline) and from 2008–2011 (follow-up). Baseline serum FGF21 levels were analyzed using enzyme-linked immunosorbent assay. Results: During the average 2.8-year follow-up period, 82 participants (36.6{\%}) developed new-onset MetS. Serum FGF21 levels were significantly higher in patients with new-onset MetS than in those without MetS (209.56±226.80 vs. 110.09±81.10, p<0.01). In multivariate adjusted models, the odds for MetS development were greater in patients with serum FGF21 levels in the highest quartile, compared to those in the lowest quartile (3.84, 95{\%} confidence interval: 1.59–9.28). Conclusion: Serum FGF21 level was an independent predictor for new-onset MetS in a population-based prospective study.",
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Serum fibroblast growth factor 21 and new-onset metabolic syndrome : KoGES-ARIRANG study. / Choi, Jung Ran; Kim, Jang Young; Park, Il Hwan; Huh, Ji Hye; Kim, Ki Woo; Cha, Seung Kuy; Park, Kyu Sang; Sohn, Joon Hyung; Park, Jong Taek; Koh, Sang Baek.

In: Yonsei medical journal, Vol. 59, No. 2, 03.2018, p. 287-293.

Research output: Contribution to journalArticle

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T1 - Serum fibroblast growth factor 21 and new-onset metabolic syndrome

T2 - KoGES-ARIRANG study

AU - Choi, Jung Ran

AU - Kim, Jang Young

AU - Park, Il Hwan

AU - Huh, Ji Hye

AU - Kim, Ki Woo

AU - Cha, Seung Kuy

AU - Park, Kyu Sang

AU - Sohn, Joon Hyung

AU - Park, Jong Taek

AU - Koh, Sang Baek

PY - 2018/3

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N2 - Purpose: Fibroblast growth factor 21 (FGF21) is a crucial metabolic regulator, with multiple favorable effects on glucose homeo-stasis and lipid metabolism. Since serum FGF21 level has been implicated as a potential marker for the early identification of metabolic syndrome (MetS), we investigated the association between serum FGF21 level and the development of MetS in a population-based prospective study. Materials and Methods: We conducted a prospective study of 221 randomly sampled adults without MetS from a general population-based cohort study who were examined from 2005–2008 (baseline) and from 2008–2011 (follow-up). Baseline serum FGF21 levels were analyzed using enzyme-linked immunosorbent assay. Results: During the average 2.8-year follow-up period, 82 participants (36.6%) developed new-onset MetS. Serum FGF21 levels were significantly higher in patients with new-onset MetS than in those without MetS (209.56±226.80 vs. 110.09±81.10, p<0.01). In multivariate adjusted models, the odds for MetS development were greater in patients with serum FGF21 levels in the highest quartile, compared to those in the lowest quartile (3.84, 95% confidence interval: 1.59–9.28). Conclusion: Serum FGF21 level was an independent predictor for new-onset MetS in a population-based prospective study.

AB - Purpose: Fibroblast growth factor 21 (FGF21) is a crucial metabolic regulator, with multiple favorable effects on glucose homeo-stasis and lipid metabolism. Since serum FGF21 level has been implicated as a potential marker for the early identification of metabolic syndrome (MetS), we investigated the association between serum FGF21 level and the development of MetS in a population-based prospective study. Materials and Methods: We conducted a prospective study of 221 randomly sampled adults without MetS from a general population-based cohort study who were examined from 2005–2008 (baseline) and from 2008–2011 (follow-up). Baseline serum FGF21 levels were analyzed using enzyme-linked immunosorbent assay. Results: During the average 2.8-year follow-up period, 82 participants (36.6%) developed new-onset MetS. Serum FGF21 levels were significantly higher in patients with new-onset MetS than in those without MetS (209.56±226.80 vs. 110.09±81.10, p<0.01). In multivariate adjusted models, the odds for MetS development were greater in patients with serum FGF21 levels in the highest quartile, compared to those in the lowest quartile (3.84, 95% confidence interval: 1.59–9.28). Conclusion: Serum FGF21 level was an independent predictor for new-onset MetS in a population-based prospective study.

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