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. Author manuscript; available in PMC: 2019 May 1.
Published in final edited form as: J Acquir Immune Defic Syndr. 2018 May 1;78(1):54–61. doi: 10.1097/QAI.0000000000001641

Table 1.

Baseline characteristics of participants started on isoniazid preventive therapy in the REMEMBER trial (N=426)

Characteristics n (%) or median (IQR)*
Age (years)   35 (30–42)
Sex
  Male 226 (53%)
  Female 200 (47%)
Race
  Black African or black of African origin 388 (91%)
  Other   38 (9%)
Country
 Malawi   98 (23%)
 South Africa   90 (21%)
 Kenya   75 (18%)
 Haiti   56 (13%)
 Zimbabwe   27 (6%)
 Uganda   24 (6%)
 Peru   19 (4%)
 Zambia   19 (4%)
 India   12 (3%)
 Brazil     6 (1%)
Pretreatment AST/ALT
  Normal 327 (77%)
  Raised   99 (23%)
Hepatitis B surface antigen
 Negative 384 (94%)
 Positive   26 (6%)
APRI score§
 <=1.5 412 (97%)
 >1.5   12 (3%)
Karnofsky Score
 80–100 371 (87%)
 0–70   55 (13%)
CD4 cell count (cells per μL) 19.0 (9–33)
Hemoglobin (g/dL) 11.3 (10.2–12.6)
HIV-1 RNA (log10 copies per mL)   5.3 (4·9–5·7)
Hospital admission within the past 30 days   23 (5%)
Body-mass index <18·5 kg/m2 128 (30%)
Alcohol intake
 Never 214 (50%)
 Takes alcohol   33 (8%)
 No answer 179 (42%)
*

IQR = Interquartile range

Raised pretreatment AST/ALT defined as AST and/or ALT elevations at ≥1.25× ULN and <2.5×ULN at study entry.

16 values were missing

§

2 values were missing