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. Author manuscript; available in PMC: 2021 Aug 1.
Published in final edited form as: J Rheumatol. 2019 Nov 15;47(8):1209–1217. doi: 10.3899/jrheum.190684

Table 5.

Characteristics and outcomes of LN cases with two APOL1 risk alleles.

Case 1 Case 2 Case 3 Case 4
Age at recruitment 28 51 29 32
Sex Female Female Female Female
Ancestry Black Mixed Black Mixed
SLICC criteria 8 5 4 8
LN duration, months 120 47 70 42
Kidney biopsy LN class IV-S LN class IV-G/V LN class IV-S/V LN class V
Crescents, % 10 0 0 0
Global sclerosis, % 36.8 25 25 0
TA/IF, % 50–75 50–75 <25 <25
AI/CI 3/6 NA 6/4 0/2
Treatment CF, MMF, steroids CF, MMF, steroids CF, MMF, CsA, steroids CF, MMF, steroids
eGFR, mL/min (CKD-EPI) last follow-up 28 18 140 113
Outcome CKD stage 4 CKD stage 4 Partial response Complete response
APOL1 genotype G1G1 G1G1 G1G1 G1G1

Abbreviations: SLICC, Systemic Lupus International Collaborating Clinics Classification Criteria; LN, lupus nephritis; TA, tubular atrophy; IF, interstitial fibrosis; AI, activity index; CI, chronicity index; NA, not available; CF, cyclophosphamide; MMF, mycophenolate mofetil; CsA, cyclosporine; CKD, chronic kidney disease.