Urine 6-Bromotryptophan: Associations with Genetic Variants and Incident End-Stage Kidney Disease

Sekula P, Tin A, Schultheiss UT, Baid-Agrawal S, Mohney RP, Steinbrenner I, Yu B, Luo S, Boerwinkle E, Eckardt KU, Coresh J, Grams ME, Kӧttgen A (2020)


Publication Type: Journal article

Publication year: 2020

Journal

Book Volume: 10

Article Number: 10018

Journal Issue: 1

DOI: 10.1038/s41598-020-66334-w

Abstract

Higher serum 6-bromotryptophan has been associated with lower risk of chronic kidney disease (CKD) progression, implicating mechanisms beyond renal clearance. We studied genetic determinants of urine 6-bromotryptophan and its association with CKD risk factors and incident end-stage kidney disease (ESKD) in 4,843 participants of the German Chronic Kidney Disease (GCKD) study. 6-bromotryptophan was measured from urine samples using mass spectrometry. Patients with higher levels of urine 6-bromotryptophan had higher baseline estimated glomerular filtration rate (eGFR, p < 0.001). A genome-wide association study of urine 6-bromotryptophan identified two significant loci possibly related to its tubular reabsorption, SLC6A19, and its production, ERO1A, which was also associated with serum 6-bromotryptophan in an independent study. The association between urine 6-bromotryptophan and time to ESKD was assessed using Cox regression. There were 216 ESKD events after four years of follow-up. Compared with patients with undetectable levels, higher 6-bromotryptophan levels were associated with lower risk of ESKD in models unadjusted and adjusted for ESKD risk factors other than eGFR (

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APA:

Sekula, P., Tin, A., Schultheiss, U.T., Baid-Agrawal, S., Mohney, R.P., Steinbrenner, I.,... Kӧttgen, A. (2020). Urine 6-Bromotryptophan: Associations with Genetic Variants and Incident End-Stage Kidney Disease. Scientific Reports, 10(1). https://doi.org/10.1038/s41598-020-66334-w

MLA:

Sekula, Peggy, et al. "Urine 6-Bromotryptophan: Associations with Genetic Variants and Incident End-Stage Kidney Disease." Scientific Reports 10.1 (2020).

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