| Autor: |
Bramble, Matthew S., Fourcassié, Victor, Vashist, Neerja, Roux-Dalvai, Florence, Zhou, Yun, Bumoko, Guy, Kasendue, Michel Lupamba, Spencer, D'Andre, Musasa Hanshi-Hatuhu, Hilaire, Kambale-Mastaki, Vincent, Manalo, Rafael Vincent M., Mohammed, Aliyah, McIlwain, David R., Cunningham, Gary, Summar, Marshall, Boivin, Michael J., Caldovic, Ljubica, Vilain, Eric, Mumba-Ngoyi, Dieudonne, Tshala-Katumbay, Desire |
| Předmět: |
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| Zdroj: |
Nature Communications; 9/6/2024, Vol. 15 Issue 1, p1-14, 14p |
| Abstrakt: |
Konzo is a neglected paralytic neurological disease associated with food (cassava) poisoning that affects the world's poorest children and women of childbearing ages across regions of sub-Saharan Africa. Despite understanding the dietary factors that lead to konzo, the molecular markers and mechanisms that trigger this disease remain unknown. To identify potential protein biomarkers associated with a disease status, plasma was collected from two independent Congolese cohorts, a discovery cohort (n = 60) and validation cohort (n = 204), sampled 10 years apart and subjected to multiple high-throughput assays. We identified that Glutathione Peroxidase 3 (GPx3), a critical plasma-based antioxidant enzyme, was the sole protein examined that was both significantly and differentially abundant between affected and non-affected participants in both cohorts, with large reductions observed in those affected with konzo. Our findings raise the notion that reductions in key antioxidant mechanisms may be the biological risk factor for the development of konzo, particularly those mediated through pathways involving the glutathione peroxidase family. The search for biomarkers associated with konzo disease has been a long-standing question within the research community. Here, the authors have uncovered a potential biomarker for konzo that is associated with the ability to manage oxidative damage. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
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