Associations of plasma very-long-chain SFA and the metabolic syndrome in adults

Jing Zhao, Xiaofan Li, Xiang Li, Qianqian Chu, Yunhua Zhou, Zi Li, Hong Zhang, Thomas J. Brenna, Yiqing Song, Ying Gao

Research output: Contribution to journalArticle

Abstract

Plasma levels of very-long-chain SFA (VLCSFA) are associated with the metabolic syndrome (MetS). However, the associations may vary by different biological activities of individual VLCSFA or population characteristics. We aimed to examine the associations of VLCSFA and MetS risk in Chinese adults. Totally, 2008 Chinese population aged 35-59 years were recruited and followed up from 2010 to 2012. Baseline MetS status and plasma fatty acids data were available for 1729 individuals without serious diseases. Among 899 initially metabolically healthy individuals, we identified 212 incident MetS during the follow-up. Logistic regression analysis was used to estimate OR and 95 % CI. Cross-sectionally, each VLCSFA was inversely associated with MetS risk; comparing with the lowest quartile, the multivariate-adjusted OR for the highest quartile were 0·18 (95 % CI 0·13, 0·25) for C20 : 0, 0·26 (95 % CI 0·18, 0·35) for C22 : 0, 0·19 (95 % CI 0·13, 0·26) for C24 : 0 and 0·16 (0·11, 0·22) for total VLCSFA (all P for trend<0·001). The associations remained significant after further adjusting for C16 : 0, C18 : 0, C18 : 3n-3, C22 : 6n-3, n-6 PUFA and MUFA, respectively. Based on follow-up data, C20 : 0 or C22 : 0 was also inversely associated with incident MetS risk. Among the five individual MetS components, higher levels of VLCSFA were most strongly inversely associated with elevated TAG (≥1·7 mmol/l). Plasma levels of VLCSFA were significantly and inversely associated with MetS risk and individual MetS components, especially TAG. Further studies are warranted to confirm the findings and explore underlying mechanisms.

Original languageEnglish (US)
Pages (from-to)855-862
Number of pages8
JournalBritish Journal of Nutrition
Volume120
Issue number8
DOIs
StatePublished - Oct 28 2018

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Population Characteristics
Fatty Acids
Logistic Models
Regression Analysis
Population

Keywords

  • Cross-sectional studies
  • Follow-up studies
  • Hypertriacylglycerolaemia
  • Metabolic syndrome
  • SFA

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Nutrition and Dietetics

Cite this

Associations of plasma very-long-chain SFA and the metabolic syndrome in adults. / Zhao, Jing; Li, Xiaofan; Li, Xiang; Chu, Qianqian; Zhou, Yunhua; Li, Zi; Zhang, Hong; Brenna, Thomas J.; Song, Yiqing; Gao, Ying.

In: British Journal of Nutrition, Vol. 120, No. 8, 28.10.2018, p. 855-862.

Research output: Contribution to journalArticle

Zhao, J, Li, X, Li, X, Chu, Q, Zhou, Y, Li, Z, Zhang, H, Brenna, TJ, Song, Y & Gao, Y 2018, 'Associations of plasma very-long-chain SFA and the metabolic syndrome in adults', British Journal of Nutrition, vol. 120, no. 8, pp. 855-862. https://doi.org/10.1017/S0007114518002106
Zhao, Jing ; Li, Xiaofan ; Li, Xiang ; Chu, Qianqian ; Zhou, Yunhua ; Li, Zi ; Zhang, Hong ; Brenna, Thomas J. ; Song, Yiqing ; Gao, Ying. / Associations of plasma very-long-chain SFA and the metabolic syndrome in adults. In: British Journal of Nutrition. 2018 ; Vol. 120, No. 8. pp. 855-862.
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abstract = "Plasma levels of very-long-chain SFA (VLCSFA) are associated with the metabolic syndrome (MetS). However, the associations may vary by different biological activities of individual VLCSFA or population characteristics. We aimed to examine the associations of VLCSFA and MetS risk in Chinese adults. Totally, 2008 Chinese population aged 35-59 years were recruited and followed up from 2010 to 2012. Baseline MetS status and plasma fatty acids data were available for 1729 individuals without serious diseases. Among 899 initially metabolically healthy individuals, we identified 212 incident MetS during the follow-up. Logistic regression analysis was used to estimate OR and 95 {\%} CI. Cross-sectionally, each VLCSFA was inversely associated with MetS risk; comparing with the lowest quartile, the multivariate-adjusted OR for the highest quartile were 0·18 (95 {\%} CI 0·13, 0·25) for C20 : 0, 0·26 (95 {\%} CI 0·18, 0·35) for C22 : 0, 0·19 (95 {\%} CI 0·13, 0·26) for C24 : 0 and 0·16 (0·11, 0·22) for total VLCSFA (all P for trend<0·001). The associations remained significant after further adjusting for C16 : 0, C18 : 0, C18 : 3n-3, C22 : 6n-3, n-6 PUFA and MUFA, respectively. Based on follow-up data, C20 : 0 or C22 : 0 was also inversely associated with incident MetS risk. Among the five individual MetS components, higher levels of VLCSFA were most strongly inversely associated with elevated TAG (≥1·7 mmol/l). Plasma levels of VLCSFA were significantly and inversely associated with MetS risk and individual MetS components, especially TAG. Further studies are warranted to confirm the findings and explore underlying mechanisms.",
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AU - Zhou, Yunhua

AU - Li, Zi

AU - Zhang, Hong

AU - Brenna, Thomas J.

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AB - Plasma levels of very-long-chain SFA (VLCSFA) are associated with the metabolic syndrome (MetS). However, the associations may vary by different biological activities of individual VLCSFA or population characteristics. We aimed to examine the associations of VLCSFA and MetS risk in Chinese adults. Totally, 2008 Chinese population aged 35-59 years were recruited and followed up from 2010 to 2012. Baseline MetS status and plasma fatty acids data were available for 1729 individuals without serious diseases. Among 899 initially metabolically healthy individuals, we identified 212 incident MetS during the follow-up. Logistic regression analysis was used to estimate OR and 95 % CI. Cross-sectionally, each VLCSFA was inversely associated with MetS risk; comparing with the lowest quartile, the multivariate-adjusted OR for the highest quartile were 0·18 (95 % CI 0·13, 0·25) for C20 : 0, 0·26 (95 % CI 0·18, 0·35) for C22 : 0, 0·19 (95 % CI 0·13, 0·26) for C24 : 0 and 0·16 (0·11, 0·22) for total VLCSFA (all P for trend<0·001). The associations remained significant after further adjusting for C16 : 0, C18 : 0, C18 : 3n-3, C22 : 6n-3, n-6 PUFA and MUFA, respectively. Based on follow-up data, C20 : 0 or C22 : 0 was also inversely associated with incident MetS risk. Among the five individual MetS components, higher levels of VLCSFA were most strongly inversely associated with elevated TAG (≥1·7 mmol/l). Plasma levels of VLCSFA were significantly and inversely associated with MetS risk and individual MetS components, especially TAG. Further studies are warranted to confirm the findings and explore underlying mechanisms.

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