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Peer-reviewedCC BY 4.0Nutrients

Associations Between Gut Microbiota Abundance, Dietary Purine Intake, and Fecal Short-Chain Fatty Acids Across the Clinical Spectrum of Hyperuricemia: A Cross-Sectional Study in Mexican Adults

7 more authors
15 affiliations
  1. 1Posgrado en Ciencias Biológicas, Universidad Nacional Autónoma de México, Unidad de Posgrado, Edificio D, 1° Piso, Circuito de Posgrados, Ciudad Universitaria, Coyoacán, Mexico City 04510, Mexico.
  2. 2Laboratorio de Gerociencias, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra, Calz México-Xochimilco 289, Coapa, Col. Arenal de Guadalupe, Tlalpan, Mexico City 14389, Mexico.
  3. 3Departamento de Fisiología de la Nutrición, Instituto Nacional de Ciencias, Médicas y Nutrición Salvador Zubirán, Mexico City 14080, Mexico.
  4. 4Departamento de Fisiopatología Cardio-Renal, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano 1, Belisario Domínguez Secc 16, Tlalpan, Mexico City 14080, Mexico.
  5. 5Departamento de Fisiología, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano 1, Belisario Domínguez Secc 16, Tlalpan, Mexico City 14080, Mexico.
  6. 6Universidad de la Salud (UNISA), Vasco de Quiroga 1345, Sta Fé, Álvaro Obregón, Mexico City 01210, Mexico.
  7. 7Servicio de Reumatología, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra, Calz México-Xochimilco 289, Coapa, Col. Arenal de Guadalupe, Tlalpan, Mexico City 14389, Mexico.
  8. 8Laboratorio de Microbiología Clínica, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra, Calz México-Xochimilco 289, Coapa, Col. Arenal de Guadalupe, Tlalpan, Mexico City 14389, Mexico.
  9. 9Facultad de Ciencias de la Salud, Universidad Anáhuac Campus Sur, Av. de los Tanques 865, Torres de Potrero, Álvaro Obregón, Mexico City 01840, Mexico.
  10. 10Dental Public Health Department, Division of Graduate Studies and Research, School of Dentistry, Univesidad Nacional Autónoma de México, Mexico City 04510, Mexico.
  11. 11Departamento de Inmunología, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano 1, Belisario Domínguez Secc 16, Tlalpan, Mexico City 14080, Mexico.
  12. 12Investigadora por México, Secretaría de Ciencia, Humanidades, Tecnología e Innovación, Avenida Insurgentes Sur 1582, Crédito Constructor, Mexico City 03940, Mexico.
  13. 13Subdirección de Investigación, Instituto Nacional de Cardiología Ignacio Chávez, Juan Badiano 1, Belisario Domínguez Secc 16, Tlalpan, Mexico City 14080, Mexico.
  14. 14Dirección General, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra, Calz México-Xochimilco 289, Coapa, Col. Arenal de Guadalupe, Tlalpan, Mexico City 14389, Mexico.
  15. 15Servicio de Reumatología, Hospital General de México Eduardo Liceaga, Dr. Balmis 148, Doctores, Cuauhtémoc, Mexico City 06720, Mexico.

Abstract

Background: Hyperuricemia and gout are closely associated with alterations in gut microbiota function. Short-chain fatty acids (SCFAs) produced by intestinal microorganisms may modulate immune responses and inflammation relevant to gout pathophysiology. This study evaluated fecal SCFA concentrations, their associations with dietary purine intake, and the relationship between Akkermansia spp. and Prevotella spp. abundance and fecal SCFA profiles across the clinical spectrum of hyperuricemia. Methods: This cross-sectional study included 380 Mexican adults: normouricemic controls (n = 141), individuals with asymptomatic hyperuricemia (AH; n = 98), and patients with gout (n = 141). Fecal SCFAs were quantified by GC-FID and bacterial abundance by qPCR. Dietary intake was assessed by semi-quantitative food frequency questionnaire and classified by purine content. Between-group differences were evaluated by the Kruskal–Wallis test (Benjamini–Hochberg correction); multivariable linear regression adjusted for age, sex, and BMI was used to assess associations, including a pre-specified dietary purine intake per clinical group interaction term. Results: Fecal acetate and propionate were significantly higher in gout patients than controls, whereas AH individuals had significantly higher butyrate. Moderate-purine food intake showed opposing associations with fecal acetate in controls (β = +3.61, p = 0.019) and gout patients (β = −4.59, p = 0.036), with a significant interaction (p = 0.004). Exploratory analyses revealed a positive association between Prevotella spp. abundance and fecal acetate exclusively in the gout group (β = 0.085, p = 0.020). Conclusion: These findings suggest distinct fecal SCFA profiles across stages of urate-related disease, with a disease-specific gut metabolic response to dietary purine intake potentially contributing to the inflammatory environment of established gout. Longitudinal studies with whole-microbiome profiling are needed to establish causality.

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BibTeX
@article{fuentesbello2026associations,
  title = {{Associations Between Gut Microbiota Abundance, Dietary Purine Intake, and Fecal Short-Chain Fatty Acids Across the Clinical Spectrum of Hyperuricemia: A Cross-Sectional Study in Mexican Adults}},
  author = {Alim Caelli Fuentes-Bello and Karla Vanessa Guevara-Gonzalez and Omar Granados-Portillo and Laura Gabriela Sánchez-Lozada and Ricardo Jasso-Chávez and David Galeana-Cadena and Efrén Altamirano-Molina and Brígida Herrera-López and Laura Edith Martínez-Gómez and Carlos Martínez-Armenta and Luis Esaú López-Jácome and Regina Matesanz Sánchez Azcona and Mireya Martínez-García and Luis M Amezcua-Guerra and Guadalupe Gutiérrez-Esparza and Carlos Pineda and Janitzia Vázquez-Mellado and Alberto G López-Reyes and Gabriela Angélica Martínez-Nava},
  journal = {Nutrients},
  year = {2026},
  month = oct,
  doi = {10.3390/nu18203326},
  url = {https://www.mdpi.com/2072-6643/18/20/3326},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Associations Between Gut Microbiota Abundance, Dietary Purine Intake, and Fecal Short-Chain Fatty Acids Across the Clinical Spectrum of Hyperuricemia: A Cross-Sectional Study in Mexican Adults
AU  - Alim Caelli Fuentes-Bello
AU  - Karla Vanessa Guevara-Gonzalez
AU  - Omar Granados-Portillo
AU  - Laura Gabriela Sánchez-Lozada
AU  - Ricardo Jasso-Chávez
AU  - David Galeana-Cadena
AU  - Efrén Altamirano-Molina
AU  - Brígida Herrera-López
AU  - Laura Edith Martínez-Gómez
AU  - Carlos Martínez-Armenta
AU  - Luis Esaú López-Jácome
AU  - Regina Matesanz Sánchez Azcona
AU  - Mireya Martínez-García
AU  - Luis M Amezcua-Guerra
AU  - Guadalupe Gutiérrez-Esparza
AU  - Carlos Pineda
AU  - Janitzia Vázquez-Mellado
AU  - Alberto G López-Reyes
AU  - Gabriela Angélica Martínez-Nava
PY  - 2026
DA  - 2026/10/10
JO  - Nutrients
DO  - 10.3390/nu18203326
UR  - https://www.mdpi.com/2072-6643/18/20/3326
AB  - Background: Hyperuricemia and gout are closely associated with alterations in gut microbiota function. Short-chain fatty acids (SCFAs) produced by intestinal microorganisms may modulate immune responses and inflammation relevant to gout pathophysiology. This study evaluated fecal SCFA concentrations, their associations with dietary purine intake, and the relationship between Akkermansia spp. and Prevotella spp. abundance and fecal SCFA profiles across the clinical spectrum of hyperuricemia. Methods: This cross-sectional study included 380 Mexican adults: normouricemic controls (n = 141), individuals with asymptomatic hyperuricemia (AH; n = 98), and patients with gout (n = 141). Fecal SCFAs were quantified by GC-FID and bacterial abundance by qPCR. Dietary intake was assessed by semi-quantitative food frequency questionnaire and classified by purine content. Between-group differences were evaluated by the Kruskal–Wallis test (Benjamini–Hochberg correction); multivariable linear regression adjusted for age, sex, and BMI was used to assess associations, including a pre-specified dietary purine intake per clinical group interaction term. Results: Fecal acetate and propionate were significantly higher in gout patients than controls, whereas AH individuals had significantly higher butyrate. Moderate-purine food intake showed opposing associations with fecal acetate in controls (β = +3.61, p = 0.019) and gout patients (β = −4.59, p = 0.036), with a significant interaction (p = 0.004). Exploratory analyses revealed a positive association between Prevotella spp. abundance and fecal acetate exclusively in the gout group (β = 0.085, p = 0.020). Conclusion: These findings suggest distinct fecal SCFA profiles across stages of urate-related disease, with a disease-specific gut metabolic response to dietary purine intake potentially contributing to the inflammatory environment of established gout. Longitudinal studies with whole-microbiome profiling are needed to establish causality.
SN  - 2072-6643
ER  -