Abstract Introduction: Untreated urinary tract infections (UTIs) can lead to complications, including renal deterioration due to upper urinary tract involvement. Proteinuria, characterized by excessive protein in the urine, is often indicative of kidney damage. The protein-to-creatinine ratio (P/C ratio) test is a convenient and reliable method for assessing proteinuria. This study aimed to evaluate the urine protein-to-creatinine ratio (UPCR) in UTI patients and its association with renal impairment. Materials and Methods: Eighty patients with confirmed UTI and suspected proteinuria were recruited. Urine screening included pyuria (white blood cell presence) as an initial indicator of UTI, followed by microscopic examination of centrifuged urinary sediments. The urine supernatant was analyzed for protein using the urine strip method. Results: After applying exclusion criteria, forty-six patients (n=46) were included in the statistical analysis. Of these, 26% had normal proteinuria (<15 mg/mM Cr), 35% had moderate proteinuria (15-50 mg/mM Cr), and 39% exhibited severe proteinuria (>50 mg/mM Cr). Patients were categorized into three stages (I, II, and III) with mean creatinine excretion values of 33.9 +/- 13.9 mg/dL, 31.2 +/- 17.2 mg/dL, and 29 +/- 13.6 mg/dL, respectively, all significantly below the reference interval (168 +/- 132 mg/dL). Conclusion: Increased urinary protein excretion correlates with heightened risk of renal complications, a leading factor in mortality. Urinary protein excretion was markedly elevated in Stage III patients. The P/C ratio proved to be a more accurate diagnostic marker within the urine profile, highlighting proteinuria in UTI patients as a potential risk factor for renal impairment. Keywords: proteinuria; protein to creatinine ratio (P/C ratio); urine microprotein (UmiP); urinary tract infection (UTI).
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
The study protocol was approved by the Institutional Human Ethics Committee (RGCB IHEC) of Rajiv Gandhi University of Health Sciences (registration no: DCGI - ECR/484/Inst/KL/2013, DHR-EC/NEW/INST/2020/477)
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
留言 (0)