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. Author manuscript; available in PMC: 2019 Dec 1.
Published in final edited form as: Kidney Int. 2018 Oct 2;94(6):1189–1198. doi: 10.1016/j.kint.2018.06.024

Table 5:

Clinico-pathologic characteristics of patients who received renal allografts from donors with APOL1 high-risk genotypes

Subjects Patient
#8
Patient
#11
Patient
#12
Patient
#14
Patient
#25
Patient
#27
Patient
#35
Patient
#37
Patient
#38
Donor race Hispanic AA AA AA AA AA AA AA AA
Allograft source L D D D D D D L D
APOL1 testing
specimen
Post-rep Post-rep Non-
infl Bx
Post-rep Blood Blood Post-rep Blood Blood
Post-transplant
interval to
biopsy (days)
602 173 653 86 423 229 505 1489 425
Concurrent
comorbidities,
namely AR,
viral infection,
or acute VOD
AR AR AR AR Prior
AR
Prior
CMV
CMV AR AR Prior
CMV
Serum Cr at
biopsy (mg/dL)
9.7 2.5 6.5 7.2 5.5 6.4 1.7 7.9 5.2
Urine protein/Cr
at biopsy (g/g)
3.8 2.2 6.9 2 3.5 15 6 11.6 7.6
Collapsed
glomeruli (%)
31 13 17 15 13 33 28 12 25

- Abbreviations: AA, African American; AR, acute rejection; Cr, creatinine; D, deceased donor; L, living donor; Non-infl Bx, non-inflamed biopsy performed at 1 month post-transplantation; Post-rep: post-reperfusion biopsy, VOD, vaso-occlusive disease

- Recipient #25 and #38 received their allografts from the same donor

Recipients #25 had CMV infection 230 days before index biopsies which persisted till 217 days before index biopsy and a biopsy with borderline changes 209 days prior to index biopsy

Recipients #38 had CMV infection 71 days before index biopsies which persisted till 57 days before index biopsy