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. 2024 Aug 20;5(8):101688. doi: 10.1016/j.xcrm.2024.101688

Table 2.

Effect estimates of genetically proxied SGLT2 inhibition on total, aggressive, and early-onset prostate cancer among men in general population using data from the PRACTICAL and GAME-ON/ELLIPSE Consortium

Exposure Outcome No. of cases Model Odds ratio (95% CI) p value
Genetically proxied SGLT2 inhibition total prostate cancer 79,148 inverse variance weighted MR 0.56 (0.38–0.82) 0.003
advanced prostate cancer 15,167 inverse variance weighted MR 0.52 (0.27–0.99) 0.049
early-onset prostate cancer 6,988 inverse variance weighted MR 0.27 (0.11–0.71) 0.008
advanced vs. non-advanced 14,160 inverse variance weighted MR 0.86 (0.35–2.13) 0.75
high vs. low aggressive 15,561 inverse variance weighted MR 1.14 (0.38–3.39) 0.81
high vs. low + intermediate aggressive 20,658 inverse variance weighted MR 0.69 (0.37–1.28) 0.24

Notation: advanced prostate cancer was defined as metastatic disease or Gleason score (GS) ≥ 8 or PSA > 100 or prostate cancer death; early-onset refers to prostate cancer onset before age 55; low aggressive refers to T stage from the TNM staging ≤ T1, and GS ≤ 6, and PSA < 10; intermediate aggressive refers to T stage: T2, and GS = 7, and PSA 10∼20; and high aggressive refers to T stage: T3/T4 or N1 or M1 or GS ≥ 8 or PSA > 20. Odds ratio means the reduced odds of prostate cancer risk per standard deviation unit (0.62%) reduction of HbA1c through SGLT2 inhibition.