Abstract

BackgroundPolycystic kidney disease (PKD) is a common renal disorder affecting approximately 1 in 1000 live births. Tuberculosis (TB) is an infectious disease worldwide. This study investigated the risk of TB infection in patients with PKD.MethodsA nationwide population-based cohort study was performed using Taiwan’s National Health Insurance Research Database. We used patients’ hospitalization files for the entire analysis during 2000–2012. As per diagnosis, we divided patients into PKD and non-PKD cohorts and the major outcome was TB infection.ResultsA total of 13,540 participants with 6770 patients in each cohort were enrolled. The PKD cohort had a higher risk of TB infection than did the non-PKD cohort after adjusting for age, sex, and comorbidities (adjusted hazard ratio (aHR) = 1.91, 95% confidence interval [CI] = 1.51–2.43). When classifying by sites of pulmonary TB (PTB) and extrapulmonary TB (EPTB), the PKD cohort demonstrated a significantly higher risk of EPTB (aHR = 2.44, 95% CI = 1.46–4.08) as well as a risk of PTB (aHR = 1.69, 95% CI = 1.29–2.22). When stratified by the presence or absence of a comorbidity, high TB infection risk was noted in the PKD patients without any comorbidity (HR = 2.69, 95% CI = 1.69–4.30).ConclusionsTaken together, our findings suggest that PKD is associated with a 1.91-fold increased risk of TB infection. Medical professionls should maintain a high index of suspicion in daily practice for patients with PKD, particularly those with EPTB infection.

Highlights

  • Polycystic kidney disease (PKD) is a common renal disorder affecting approximately 1 in 1000 live births

  • Compared with the non-PKD group, the PKD group displayed a significantly higher risk of TB after adjusting for age, sex, and comorbidities

  • When the analysis was classified into pulmonary TB (PTB) and extrapulmonary TB (EPTB), the PKD group exhibited a significantly higher risk of extrapul‐ monary TB (EPTB) and displayed a difference in the risk of PTB when compared with the non-PKD group

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Summary

Introduction

Polycystic kidney disease (PKD) is a common renal disorder affecting approximately 1 in 1000 live births. Chiu et al J Transl Med (2021) 19:253 and that it is the fourth leading cause of end-stage renal disease (ESRD) after diabetes mellitus, hypertension, and glomerulonephritis in the United States [2]. PKD is the most common congenital renal disease caused by a mutation in the PKD1 gene on chromosome 16 and PKD2 gene on chromosome 4 accounting for 85% and 15% of the disease, respectively [6]. The renal manifestations of PKD include urine-concentrating defect, hematuria, nephrolithiasis, urinary tract infection, flank or abdominal pain, hypertension, proteinuria, chronic kidney disease, and ESRD [8,9,10]. 5% of the total number of ESRD cases are caused by PKD in the United States [11, 12]

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