Skip to main content
. Author manuscript; available in PMC: 2021 Dec 1.
Published in final edited form as: J Acquir Immune Defic Syndr. 2020 Dec 1;85(4):489–497. doi: 10.1097/QAI.0000000000002464

Table 1.

Baseline characteristics of participants in TAHOD and TAHOD-LITE

TAHOD (Full risk score) TAHOD-LITE (Short risk score)
Developed CKD Did not develop CKD All Developed CKD Did not develop CKD All
N (%) N (%) N (%) N (%) N (%) N (%)
Total 391 (100) 5701 (100) 6092 (100) 520 (100) 9197 (100) 9717 (100)
Sex
 Female 106 (27.1) 1824 (32) 1930 (31.7) 117 (22.5) 2410 (26.2) 2527 (26)
 Male 285 (72.9) 3877 (68) 4162 (68.3) 403 (77.5) 6787 (73.8) 7190 (74)
Age group
 ≤35 66 (16.9) 2993 (52.5) 3059 (50.2) 30 (5.8) 4011 (43.6) 4041 (41.6)
 36-50 176 (45) 2328 (40.8) 2504 (41.1) 222 (42.7) 4099 (44.6) 4321 (44.5)
 51-60 102 (26.1) 305 (5.3) 407 (6.7) 151 (29) 830 (9) 981 (10.1)
 61+ 47 (12) 75 (1.3) 122 (2) 117 (22.5) 257 (2.8) 374 (3.8)
HIV exposure
 Not intravenous drug user 379 (96.9) 5342 (93.7) 5721 (93.9) 515 (99.0) 8905 (96.8) 9420 (96.9)
 Intravenous drug user 12 (3.1) 359 (6.3) 371 (6.1) 5 (1) 292 (3.2) 297 (3.1)
Nadir CD4 count (cells/m3)
 ≤200 290 (74.2) 3381 (59.3) 3671 (60.3) 320 (61.5) 4264 (46.4) 4584 (47.2)
 >200 101 (25.8) 2320 (40.7) 2421 (39.7) 200 (38.5) 4933 (53.6) 5133 (52.8)
ART initiation year
 ≤2002 103 (26.3) 610 (10.7) 713 (11.7) 49 (9.4) 390 (4.2) 439 (4.5)
 2003-2005 79 (20.2) 983 (17.2) 1062 (17.4) 56 (10.8) 762 (8.3) 818 (8.4)
 2006-2009 131 (33.5) 1942 (34.1) 2073 (34) 206 (39.6) 2917 (31.7) 3123 (32.1)
 ≥2010 78 (19.9) 2111 (37) 2189 (35.9) 174 (42.6) 192 (36.9) 5062 (52.1)
 not started 0 (0) 55 (1) 55 (0.9) 17 (4.2) 17 (3.3) 275 (2.8)
Hepatitis C coinfection
 Negative 362 (92.6) 5069 (88.9) 5431 (89.1) 503 (96.7) 8688 (94.5) 9191 (94.6)
 Positive 29 (7.4) 632 (11.1) 661 (10.9) 17 (3.3) 509 (5.5) 526 (5.4)
Hypertension
 No 218 (55.8) 3141 (55.1) 3359 (55.1)
 Yes 3 (0.8) 13 (0.2) 16 (0.3)
 Unknown/missing 170 (43.5) 2547 (44.7) 2717 (44.6)
Diabetes mellitus
 No 229 (58.6) 3267 (57.3) 3496 (57.4
 Yes 23 (5.9) 43 (0.8) 66 (1.1)
 Unknown/missing 139 (35.6) 2391 (41.9) 2530 (41.5)
Prior CVD
 No/not reported 374 (95.7) 5671 (99.5) 6045 (99.2)
 Yes 17 (4.3) 30 (0.5) 47 (0.8)
Baseline eGFR
 61-70 106 (27.1) 285 (5) 391 (6.4) 129 (24.8) 347 (3.8) 476 (4.9)
 71-90 167 (42.7) 1276 (22.4) 1443 (23.7) 220 (42.3) 1764 (19.2) 1984 (20.4)
 >90 118 (30.2) 4140 (72.6) 4258 (69.9) 171 (32.9) 7086 (77) 7257 (74.7)
Starting potentially nephrotoxic ARVs after baseline
 TDF 271 (69.3) 3441 (60.4) 3712 (60.9) 337 (64.8) 6432 (69.9) 6762 (69.6)
 ATV 27 (6.9) 350 (6.1) 377 (6.2) 24 (4.6) 434 (4.7) 458 (4.7)
 ATV/r 42 (10.7) 540 (9.5) 582 (9.6) 65 (1.2) 1437 (1.6) 1502 (1.5)
 LPV/r 76 (19.4) 876 (15.4) 952 (15.6) 35 (6.7) 914 (9.9) 949 (9.8)
 Other boosted PIs 38 (9.7) 498 (8.7) 536 (8.8) 24 (4.6) 477 (5.2) 501 (5.2)
 Any of these 298 (76.2) 4041 (70.9) 4339 (71.2) 349 (6.7) 6527 (7.1) 6878 (70.8)

The TREAT Asia HIV Observational Database (TAHOD) is a collaborative observational cohort study that involves 21 sites in the Asia and Pacific region. The participating countries are Cambodia, China and Hong Kong SAR, India, Indonesia, Japan, Malaysia, the Philippines, Singapore, South Korea, Taiwan, Thailand and Vietnam. TAHOD Low Intensity Transfer (TAHOD-LITE) study is a sub-study of TAHOD which collects demographics, hepatitis serology, ART history, and HIV-related laboratory results from all patients at 10 participating sites of 8 countries in TAHOD.

Abbreviations: CKD, chronic kidney disease; eGFR, estimated glomerular filtration rate; TDF, tenofovir disoproxil fumarate; ATV, atazanavir; ATV/r, ritonavir boosted atazanavir; LPV/r, lopinavir boosted ritonavir; PIs, protease inhibitors.