Urine and Dried Blood Spots From Children and Pregnant Women Reveal Phytochemicals, Amino Acids, and Carnitine Metabolites as Cowpea Consumption Biomarkers

Author:

Tipton Madison1,Baxter Bridget A.1,Pfluger Brigitte A.2,Sayre‐Chavez Brooke3,Muñoz‐Amatriaín María34,Broeckling Corey D.5,Shani Issah6,Steiner‐Asiedu Matilda6,Manary Mark7,Ryan Elizabeth P.1ORCID

Affiliation:

1. Department of Environmental and Radiological Health Sciences College of Veterinary Medicine and Biomedical Sciences Colorado State University Fort Collins Colorado 80523 USA

2. Nutrition and Health Sciences Laney Graduate School Emory University Atlanta Georgia 30322 USA

3. Department of Soil and Crop Sciences Colorado State University Fort Collins Colorado 80521 USA

4. Departamento de Biología Molecular ‐ Área de Genética Universidad de León León 24071 Spain

5. Analytical Resources Core: Bioanalysis and Omics Center Colorado State University Fort Collins Colorado 80523 USA

6. Department of Nutrition and Food Science College of Basic and Applied Science University of Ghana Legon Accra P.O. Box LG 134 Legon Ghana

7. Department of Pediatrics Washington University School of Medicine in St. Louis St. Louis Missouri 63110 USA

Abstract

ScopeLegumes consumption has been proven to promote health across the lifespan; cowpeas have demonstrated efficacy in combating childhood malnutrition and growth faltering, with an estimated malnutrition prevalence of 35.6% of children in Ghana. This cowpea feeding study aimed to identify a suite of metabolic consumption biomarkers in children and adults.Methods and ResultsUrine and dried blood spots (DBS) from 24 children (9‐21 months) and 21 pregnant women (>18 years) in Northern Ghana are collected before and after dose‐escalated consumption of four cowpea varieties for 15 days. Untargeted metabolomics identified significant increases in amino acids, phytochemicals, and lipids. The carnitine metabolism pathway is represented by 137 urine and 43 DBS metabolites, with significant changes to tiglylcarnitine and acetylcarnitine. Additional noteworthy candidate biomarkers are mansouramycin C, N‐acetylalliin, proline betaine, N2, N5‐diacetylornithine, S‐methylcysteine, S‐methylcysteine sulfoxide, and cis‐urocanate. S‐methylcysteine and S‐methylcysteine sulfoxide are targeted and quantified in urine.ConclusionThis feeding study for cowpea biomarkers supports the utility of a suite of key metabolites classified as amino acids, lipids, and phytochemicals for dietary legume and cowpea‐specific food exposures of global health importance.

Funder

United States Agency for International Development

Publisher

Wiley

Subject

Food Science,Biotechnology

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