Key result
Hyperuricemia during tuberculosis treatment shows no association with major adverse cardiovascular events.
Why the study?
Hyperuricemia is common during tuberculosis treatment, especially with pyrazinamide, but its relationship with major adverse cardiovascular events was unclear.
Does hyperuricemia during tuberculosis treatment increase the risk of major adverse cardiovascular events in adult TB patients?
Cohort (n=1,143)
No
Does hyperuricemia during tuberculosis treatment increase the risk of major adverse cardiovascular events in adult TB patients?
Odds Ratio: 1.505 (95% CI 0.184–12.299)
Absolute Event Rate: 0.74% vs 0.5%
p-value: p=0.703
Hyperuricemia during tuberculosis treatment is a transient phenomenon that is not associated with an increased risk of major adverse cardiovascular events and may serve as an indicator of good adherence to pyrazinamide-based therapy.
Does not support hyperuricemia as a short-term MACE predictor during TB treatment; hypothesis-generating for its link to outcomes in larger cohorts.
BACKGROUND: Hyperuricemia is common during tuberculosis (TB) treatment, especially in association with pyrazinamide (PZA). This study investigated the relationship between major adverse cardiovascular events (MACEs) and hyperuricemia during TB treatment. METHODS: We conducted a single-center retrospective cohort study. From January 2010 through June 2017, we assessed all consecutive TB patients at Chonnam National University Hospital in South Korea. Hyperuricemia was defined as serum uric acid levels exceeding 7.0 mg/dL (men) and 6.0 mg/dL (women). RESULTS: Of the 1,143 patients included, PZA was administered to 1,081 (94.6%), and hyperuricemia was detected in 941 (82.3%). Eight patients experienced MACEs. Multivariate analysis using logistic regression indicated that prior ischemic heart disease was associated with MACE development (OR,14.087; 95% CI,3.304-60.061; P < 0.000), while hyperuricemia was not (OR, 1.505; 95% CI, 0.184-12.299; P = 0.703). For patients without drug-resistant TB, the absence of hyperuricemia was associated with higher mortality (OR, 2.609; 95% CI, 1.066-6.389; P = 0.036), whereas hyperuricemia was associated with less worse outcomes (OR,0.316; 95% CI,0.173-0.576; P < 0.000). CONCLUSIONS: Although most patients treated with PZA developed hyperuricemia, it was not associated with MACE development. Hyperuricemia during TB treatment was associated with better outcomes, possibly due to consistent adherence to TB treatment.
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Shin et al. (2023) conducted a cohort in Tuberculosis (n=1,143). Hyperuricemia vs. Normouricemia was evaluated on Major adverse cardiovascular events (composite of cardiovascular death, myocardial infarction, angina, stroke, transient ischemic attack, and myocardial revascularization) (OR 1.505, 95% CI 0.184-12.299, p=0.703). Hyperuricemia during tuberculosis treatment was not significantly associated with the development of major adverse cardiovascular events (OR 1.505, 95% CI 0.184-12.299, p=0.703).
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