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. 2024 Apr;11(2):316-323.
doi: 10.1016/j.ajur.2022.08.007. Epub 2023 Mar 21.

Metabolic syndrome and the urinary microbiome of patients undergoing percutaneous nephrolithotomy

Affiliations

Metabolic syndrome and the urinary microbiome of patients undergoing percutaneous nephrolithotomy

Ryan A Dornbier et al. Asian J Urol. 2024 Apr.

Abstract

Objective: To identify possible stone-promoting microbes, we compared the profiles of microbes grown from stones of patients with and without metabolic syndrome (MetS). The association between MetS and urinary stone disease is well established, but the exact pathophysiologic relationship remains unknown. Recent evidence suggests urinary tract dysbiosis may lead to increased nephrolithiasis risk.

Methods: At the time of percutaneous nephrolithotomy, bladder urine and stone fragments were collected from patients with and without MetS. Both sample types were subjected to expanded quantitative urine culture (EQUC) and 16 S ribosomal RNA gene sequencing.

Results: Fifty-seven patients included 12 controls (21.1%) and 45 MetS patients (78.9%). Both cohorts were similar with respect to demographics and non-MetS comorbidities. No controls had uric acid stone composition. By EQUC, bacteria were detected more frequently in MetS stones (42.2%) compared to controls (8.3%) (p=0.041). Bacteria also were more abundant in stones of MetS patients compared to controls. To validate our EQUC results, we performed 16 S ribosomal RNA gene sequencing. In 12/16 (75.0%) sequence-positive stones, EQUC reliably isolated at least one species of the sequenced genera. Bacteria were detected in both "infectious" and "non-infectious" stone compositions.

Conclusion: Bacteria are more common and more abundant in MetS stones than control stones. Our findings support a role for bacteria in urinary stone disease for patients with MetS regardless of stone composition.

Keywords: Metabolic syndrome; Nephrolithiasis; Percutaneous nephrolithotomy; Urinary microbiome; Urolithiasis.

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Conflict of interest statement

Wolfe AJ is a member of the Urobiome Therapeutics (Boston, MA, USA) advisory board and the Pathnostics Scientific (Irvine, CA, USA) advisory board. Wolfe AJ has research funding from the Craig H. Neilsen Foundation, Pathnostics (Irvine, CA, USA), and an anonymous donor. The other authors declared no conflict of interest.

Figures

Figure 1
Figure 1
Growth of bacteria on expanded quantitative urine culture. (A) Urinary stone; (B) Bladder urine; (C) Stone chemical composition of the corresponding stone. The solid black line marks the division of control and metabolic syndrome patients. Each column above or below corresponds to the same patient.
Figure 2
Figure 2
16 S rRNA gene sequencing of bladder and stone samples from controls and metabolic syndrome patients. The solid black vertical lines separate paired sampled.

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