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Ensayo controlado aleatorizado2024Solo mecanismosAcceso abierto

Comprehensive modulatory effects of whole grain consumption on immune-mediated inflammation in middle-aged and elderly community residents: A real-world randomized controlled trial

Li C, Li Y, Wang N, Ge Z, Wang J, Ding B, Bi Y, Wang Y, Wang Y, Peng Z, Yang X, Wang C, Hong Z

Redox biology · 11 citas

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Solo mecanismos

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Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Solo mecanismos
Consumo medido con
No se indica

Quién lo pagó

Financiación
Financiación independiente
Universidad u hospital
Capital Medical University
Universidad u hospital
Beijing Friendship Hospital, Capital Medical University
Universidad u hospital
Capital Medical University Affiliated Beijing Friendship Hospital
Subvenciones
Beijing Friendship Hospital, Capital Medical University (BFHOS20230001); Beijing Friendship Hospital, Capital Medical University (YYZZ202137)

Según 3 financiadores declarados y la declaración de financiación del texto completo.

Publicación

Publicado
2024-09-06 · Redox Biol · vol. 76 · pág. 103337
Editorial
Elsevier BV
Citado
14 citas · más que el 93% de estudios similares · 3.1× el promedio de su campo
Impacto
Entre el 10 % más citado de su campo
Referencias
42 trabajos
Acceso
Acceso abierto (revista) · CC-BY-NC-ND
Áreas de investigación
Nutrition and Health in Aging · GDF15 and Related Biomarkers · Nutritional Studies and Diet
Palabras clave
Whole grains, Inflammation, Immune system, Consumption (sociology), Context (archaeology), Population, Medicine, Environmental health, Immunology, Biology, Food science
MeSH
cd4-positive t-lymphocytes, humans, inflammation, cytokines, diet, dietary fiber, aged, middle aged, female, male, whole grains, interleukin-22

13 autores

  • Cheng Li🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Yaru Li🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Nan Wang🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Zhiwen Ge🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Jia Wang🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Bingjie Ding🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Yanxia Bi🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Yuxia Wang🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Yisi Wang🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Zebin Peng🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Xinli Yang🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Congcong Wang🇨🇳Capital Medical University; Beijing Friendship Hospital
  • Zhongxin Hong🇨🇳 · autor de correspondenciaBeijing Friendship Hospital

Resumen

El texto original del estudio, en el idioma en que se publicó.

Background and aims

Whole grain consumption is widely recognized as a vital component of a balanced diet. Dietary fiber has been well-documented to play a crucial role in these health benefits attributed to whole grain intake. However, population-based evidence directly linking whole grain consumption to anti-inflammatory effects, especially in the context of immune-mediated inflammation, remains limited. We hypothesized that whole grain consumption promotes health by modulating immune-mediated inflammation.

Methods and results

This study was designed as a real-world, population-based randomized controlled trial. We compared the effects of whole grain versus refined grain consumption on immune-mediated inflammation through staple food substitution, while participants maintained their usual dietary practices. The results demonstrated that whole grain consumption significantly reduced circulating levels of pro-inflammatory cytokines IL-22 and IL-23 compared to refined grain consumption. These reductions were associated with optimized short-chain fatty acid profiles and changes in CD4+ T cell subset distributions.

Conclusions

The findings suggest that the anti-inflammatory effects of whole grain consumption in middle-aged and elderly populations are mediated by targeting specific CD4+ T cell subsets, in addition to modulating both upstream short-chain fatty acid composition and downstream expression of the pro-inflammatory cytokines IL-22 and IL-23.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial (CC BY-NC-ND).

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