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. 2022 Sep 2;37(1):51–59. doi: 10.1097/QAD.0000000000003376

Table 1.

Participant characteristics by HIV serostatus.

Overall HIV+KS HIVKS P
N = 200 N = 166 N = 34
Male, N (%) 156 (78) 127 (76.5) 29 (85.3) 0.26
Age, median (range) 34 (18, 90) 32 (18, 75) 46 (19, 90) <0.001
ACTG stage, N (%)
 T1 176 (88) 144 (86.7) 32 (94.1) 0.23
 I1 93 (56.4)
 S1 147 (73.5) 124 (74.7) 23 (67.6) 0.40
Karnofsky <70, N (%) 58 (29) 47 (28.3) 11 (32.4) 0.64
B-symptoms, N (%) 138 (69) 118 (71.1) 20 (58.8) 0.16
Opportunistic infections, N (%) 29 (14.5) 27 (16.3) 2 (5.9) 0.12
BMI (kg/m2), median (IRQ)a 26 (14.1) 21.5 (19.8, 23.3) 21.7 (19.7, 23.9) 0.44
Hemoglobin, median (IQR)a 10.3 (8.9, 12.5) 10 (8.7, 11.9) 12.8 (11.1, 14.9) <0.001
Platelets, median (IQR)a 232 (155, 297) 223 (138, 297) 245.5 (199, 305) 0.08
Abnormal chest X-ray finding, N (%)a,b 65 (38.7) 61 (43.9) 4 (13.7) 0.002
Months since first KS lesion, median (IQR)a 7 (3, 17) 6 (3, 12) 22 (8, 48) <0.001
Distinct sites with KS lesions 5 (2, 7) 5 (3, 7) 2 (1, 3) <0.001
Any edema, N (%) 165 (82.5) 135 (81.3) 30 (88.2) 0.33
Any macular lesions, N (%) 195 (97.5) 162 (97.6) 33 (97.1) 0.86
Any nodular lesions, N (%) 134 (67) 107 (64.5) 27 (79.4) 0.09
Any fungating lesions, N (%) 93 (46.5) 70 (42.2) 23 (67.7) 0.007
Months since HIV diagnosis, median (IQR)a 2 (1, 5)
HIV viral load, log10(copies/ml) median (IQR)c 5.3 (4.9, 5.7)
CD4+ count, median (IQR) 167 (49, 338)
KSHV detected in plasma, N (%)a 188 (95.4) 158 (96.3) 30 (90.9) 0.17
Plasma KSHV titer, log10(copies/ml), median (IQR)d 4 (3.6, 4.5) 4.1 (3.7, 4.5) 3.8 (3.1, 4) <0.001
KSHV detected in oral swaba, N (%) 115 (57.8) 101 (61.2) 14 (41.2) 0.03
Oral KSHV titer log10(copies/ml), median (IQR)e 3.6 (2.9, 4.5) 3.6 (2.9, 4.5) 3.3 (2.6, 5.1) 0.80

ACTG, AIDS Clinical Trials Group; IQR, interquartile range; KHSV, Kaposi sarcoma-associated herpesvirus; KS, Kaposi sarcoma.

a

Percentages, medians, ranges, and P-values exclude participants missing data (Table 1, Supplemental Digital Content).

b

Infiltrate or effusion, unilateral or bilateral.

c

Excludes one participant for whom viral load was not assessed, and two participants with undetectable viral load.

d

Among participants with detectable plasma KSHV.

e

Among participants with detectable oral KSHV.