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. 2015 Dec 10;11(1):81–89. doi: 10.2215/CJN.02560315

Table 4.

Multivariable Cox proportional hazard models predicting survival distribution of time to complete remission

Variablea Hazard Ratio (95% Confidence Interval)
Proteinuria
 UPC<1 g/g Reference
 UPC 1–3 g/g 0.3 (0.2 to 0.5)
 UPC>3 g/g 0.3 (0.2 to 0.5)
Cohort
 MCD Reference
 FSGS 0.2 (0.1 to 0.4)
 MN 0.4 (0.2 to 0.9)
 Other 0.5 (0.2 to 1.1)
Prior IST exposure (overall) 1.4 (0.9 to 2.2)
Prior IST exposure by cohort
 MCD, treated 0.8 (0.3 to 2.2)
 MCD, untreated Reference
 FSGS, treated 2.5 (1.1 to 5.6)
 FSGS, untreated Reference
 MN, treated 2.8 (1.0 to 8.2)
 MN, untreated Reference
 Other, treated 0.8 (0.4 to 1.6)
 Other, untreated Reference
Prospective IST exposure (overall) 1.3 (0.9 to 2.1)
Prospective IST exposure by cohort
 MCD, treated 1.8 (0.7 to 4.9)
 MCD, untreated Reference
 FSGS, treated 2.1 (1.0 to 5.1)
 FSGS, untreated Reference
 MN, treated 0.4 (0.2 to 1.2)
 MN, untreated Reference
 Other, treated 1.1 (0.6 to 2.1)
 Other, untreated Reference

All patients n=413/188 remissions. Lower hazard ratios indicate a lower likelihood of reaching complete remission. Prior IST exposure refers to medications reported before study baseline visit. UPC, urine protein-to-creatinine ratio; MCD, minimal-change disease; MN, membranous nephropathy; IST, immunosuppression therapy.

a

Significant unadjusted predictors of complete remission (P<0.05) that were removed during multivariable backward selection: family history of kidney disease, family history of hypertension, family history of diabetes, age, weight status (obese versus normal weight), eGFR, LDL cholesterol, and triglycerides.