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. 2021 Sep 27;70(12):2903–2916. doi: 10.2337/db21-0385

Table 4.

Risk of adverse outcomes within 28 days after COVID-19 diagnosis or positive SARS-CoV-2 test results

Before propensity matching After propensity matching*
n (%) RR (95% CI) P Relative change, % n after matching n (%) RR (95% CI) P Relative change, %
Hospital admissions
 No-G/D/P (n = 23,714) 6,741 (28.4) 1.04 (1.01–1.07) 0.004 4.3
  All T2DM (n = 29,516) 8,046 (27.3)
 GLP-1 (n = 1,774) 267 (15.1) 0.53 (0.47–0.59) <0.001 −47.1 1,163 183 (15.7) 0.67 (0.57–0.79) <0.001 −33.0
  No-G/D/P (n = 23,714) 6,741 (28.4) 1,163 273 (23.5)
 DPP-4 (n = 2,264) 667 (29.5) 1.04 (0.97–1.11) 0.30 3.6 2,264 667 (29.5) 0.98 (0.89–1.07) 0.63 −2.5
  No-G/D/P (n = 23,714) 6,741 (28.4) 2,264 684 (30.2)
 Pioglitazone (n = 469) 108 (23.0) 0.81 (0.69–0.96) 0.01 −19.0 340 68 (20.0) 0.71 (0.54–0.93) 0.01 −29.2
  No-G/D/P (n = 23,714) 6,741 (28.4) 340 96 (28.2)
 Any Med (n = 5,606) 1,259 (22.5) 0.79 (0.75–0.83) <0.001 −21.0 5,520 1,229 (22.3) 0.84 (0.78–0.90) <0.001 −16.2
  No-G/D/P (n = 23,714) 6,741 (28.4) 5,520 1,467 (26.6)
Respiratory complications
 No-G/D/P (n = 23,714) 6,432 (27.1) 1.06 (1.03–1.09) <0.001 5.7
  All T2DM (n = 29,516) 7,577 (25.7)
 GLP-1 (n = 1,774) 269 (15.2) 0.56 (0.50–0.63) <0.001 −44.1 1,163 178 (15.3) 0.62 (0.52–0.73) <0.001 −38.4
  No-G/D/P (n = 23,714) 6,432 (27.1) 1,163 289 (24.9)
 DPP-4 (n = 2,264) 543 (24.0) 0.88 (0.82–0.95) 0.001 −11.6 2,264 543 (24.0) 0.82 (0.74–0.90) <0.001 −18.0
  No-G/D/P (n = 23,714) 6,432 (27.1) 2,264 662 (29.2)
 Pioglitazone (n = 469) 112 (23.0) 0.88 (0.75–1.04) 0.12 −12.0 340 85 (25.0) 0.89 (0.70–1.14) 0.34 −11.5
  No-G/D/P (n = 23,714) 6,432 (27.1) 340 96 (28.2)
 Any Med (n = 5,606) 1,101 (19.6) 0.72 (0.68–0.77) <0.001 −27.6 5,520 1,083 (19.6) 0.73 (0.68–0.78) <0.001 −27.2
  No-G/D/P (n = 23,714) 6,432 (27.1) 5,520 1,488 (27.0)
Mortality
 No-G/D/P (n = 23,714) 1,443 (6.1) 1.04 (0.98–1.12) 0.21 −6.5
  All T2DM (n = 29,516) 1,921 (6.5)
 GLP-1 (n = 1,774) 44 (2.5) 0.41 (0.30–0.55) <0.001 −59.2 1,163 22 (1.9) 0.58 (0.35–0.97) 0.04 −42.1
  No-G/D/P (n = 23,714) 1,443 (6.1) 1,163 38 (3.3)
 DPP-4 (n = 2,264) 169 (7.5) 1.23 (1.05–1.43) 0.009 22.7 2,264 169 (7.5) 1.03 (0.84–1.26) 0.78 3.1
  No-G/D/P (n = 23,714) 1,443 (6.1) 2,264 164 (7.2)
 Pioglitazone (n = 469) 21 (4.5) 0.74 (0.48–1.12) 0.15 −26.4 340 17 (5.0) 1.06 (0.55–2.07) 0.86 6.3
  No-G/D/P (n = 23,714) 1,443 (6.1) 340 16 (4.7)
 Any Med (n = 5,606) 266 (4.7) 0.78 (0.69–0.89) <0.001 −22.0 5,520 254 (4.6) 0.85 (0.72–1.00) 0.05 −15.1
  No-G/D/P (n = 23,714) 1,443 (6.1) 5,520 299 (5.4)

P values indicate significance compared with the No-G/D/P cohort.

*

Propensity matching balanced cohorts according to age, sex, race, ethnicity, BMI, and the presence of essential (primary) hypertension, ischemic heart disease, cerebrovascular disease, heart failure, chronic kidney disease, or overweight and obesity in the EMR within 6 months before COVID-19 diagnosis.

The No-G/D/P cohort consisted of patients with T2DM with a diagnosis of COVID-19 or positive test results for SARS-CoV-2 who did not have any GLP-1R agonists, DPP-4 inhibitors, or pioglitazone in the EMR.

The Any Med cohort consisted of patients with T2DM with a diagnosis of COVID-19 or positive test results for SARS-CoV-2 who had GLP-1R agonists, DPP-4 inhibitors, and/or pioglitazone in the EMR.