Introduction: Sodium-glucose cotransporter 2 inhibitors (SGLT2i) are effective agents for type 2 diabetes (T2D) management, yet interindividual variability in response mechanisms remains unclear. This study examined genetic interactions influencing clinical and biochemical outcomes among SGLT2i treated patients. Methods: Data from 13,808 Qatar Biobank participants were analyzed, including 207 propensity score–matched T2D patients stratified into three groups: SGLT2i-treated, metformin monotherapy, and drug-naïve. Significant clinical traits across groups were further assessed for genotype effects within SGLT2i treated patients. Results: Compared with both comparators, SGLT2i-treated individuals showed elevated serum urea (FDR < 0.05). Genetic analysis identified an association between the WFS1 rs10010131 A allele and higher urea levels exclusively in SGLT2i treated patients (β = +0.63 mmol/L per A allele, 95% CI 0.14– 1.11, p = 0.012). This variant showed strong linkage disequilibrium (r2 = 0.95, D′ = 0.99) with rs6446482 in WFS1 . Kidney-specific eQTL data revealed reduced WFS1 expression in A-allele carriers. Discussion: These findings suggest a novel pharmacogenetic interaction between WFS1 rs10010131 and urea regulation under SGLT2i therapy. The observed effect could likely reflect a genotype-related renal adaptive response rather than dysfunction, emphasizing the potential of pharmacogenomic profiling to enhance precision treatment for T2D. Keywords: sodium-glucose cotransporter 2 inhibitors, metformin, type 2 diabetes, urea, wolframin, pharmacogenomics
Naja et al. (Wed,) studied this question.