Table 4.
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.
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.