Erythrocyte odd-chain fatty acids and the risk of cardiometabolic diseases: a prospective study and updated meta-analysis - Scorecard - MDSpire

Erythrocyte odd-chain fatty acids and the risk of cardiometabolic diseases: a prospective study and updated meta-analysis

  • By

  • Liang Sun

  • Xinming Xu

  • Huaidong Du

  • Ling Lu

  • Fumiaki Imamura

  • Qishan Yang

  • Yiping Chen

  • Yan Chen

  • Pei Pei

  • Huiyong Yin

  • Ling Yang

  • Geng Zong

  • Canqing Yu

  • Qianqian Chu

  • Jun Lv

  • Puchen Zhou

  • Dianjianyi Sun

  • Junshi Chen

  • Xiang Gao

  • Liming Li

  • Zhengming Chen

  • Xu Lin

  • on behalf of the China Kadoorie Biobank Collaborative Group

  • September 24, 2025

  • 0 min

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Clinical Scorecard: Association of Erythrocyte Odd-Chain Fatty Acids with Cardiometabolic Disease Risk: A Prospective Analysis and Updated Meta-Study

At a Glance

CategoryDetail
ConditionCardiometabolic diseases including ischemic heart disease, diabetes, and stroke
Key MechanismsInverse associations of erythrocyte odd-chain fatty acids (OCFAs) 15:0 and 17:0 with incident cardiometabolic diseases; OCFAs as biomarkers reflecting dietary intake of dairy, fish/seafood, and dietary fiber
Target PopulationAsian adults, specifically Chinese adults aged 30–79 years with varying dairy intake
Care SettingPopulation-based epidemiological and nutritional assessment settings

Key Highlights

  • Erythrocyte OCFAs 15:0 and 17:0 inversely associated with incident ischemic heart disease and diabetes in Chinese adults.
  • OCFAs correlated with dietary intake of dairy products, wheat and coarse grains, and fish/seafood in Asian populations with low dairy consumption.
  • Meta-analysis supports universal applicability of OCFAs as biomarkers for cardiometabolic disease risk across diverse populations.

Guideline-Based Recommendations

Diagnosis

  • Consider measuring erythrocyte 15:0 and 17:0 levels as biomarkers for dietary intake and cardiometabolic risk stratification.

Management

  • Promote dietary sources rich in OCFAs such as dairy, fish/seafood, and dietary fiber to potentially reduce cardiometabolic disease risk.
  • Use OCFA levels to guide personalized nutrition interventions aimed at mitigating cardiometabolic disease risks.

Monitoring & Follow-up

  • Monitor erythrocyte OCFA levels to assess adherence to dietary interventions and evaluate cardiometabolic risk changes over time.

Risks

  • Low levels of erythrocyte 15:0 and 17:0 may indicate higher risk for ischemic heart disease and diabetes.

Patient & Prescribing Data

Asian adults with varying dairy intake and risk factors for cardiometabolic diseases

Increasing dietary intake of OCFA-rich foods may serve as a modifiable strategy to lower cardiometabolic disease risk; erythrocyte OCFA levels can serve as objective biomarkers to tailor and monitor nutritional interventions.

Clinical Best Practices

  • Incorporate erythrocyte OCFA measurement in nutritional assessments for cardiometabolic risk evaluation.
  • Advocate for diverse dietary sources of OCFAs beyond dairy, including fish/seafood and dietary fiber, especially in populations with low dairy consumption.
  • Use OCFA biomarker data to personalize dietary recommendations and monitor intervention efficacy in reducing cardiometabolic disease incidence.

References

Original Source(s)

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