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. Author manuscript; available in PMC: 2022 Sep 1.
Published in final edited form as: Hepatology. 2021 Jun 22;74(3):1190–1202. doi: 10.1002/hep.31839

Table 1.

Baseline Characteristics of HIV/hepatitis B virus-coinfected persons in the North American AIDS Cohort Collaboration on Research and Design (1995–2016).

Characteristic (n=8,354)
Age (n, %)
 Median (years, IQR) 42.9 (36.2–49.2)
 <40 years 3,224 (38.6%)
 40–49 years 3,204 (38.4%)
 ≥50 years 1,926 (23.1%)
Male sex (n, %) 7,775 (93.1%)
Race (n, %)
 White 3,973 (47.6%)
 Black or African American 3,421 (41.0%)
 Asian/Pacific Islander 126 (1.4%)
 Multiracial, Other, Unknown 834 (10.0%)
Hispanic (n, %) 665 (8.4%)
Body mass index (n, %)
 Median (IQR) 24.4 (22.0–27.3)
 Underweight (<18.50 kg/m2) 273 (3.6%)
 Normal (18.50–24.99 kg/m2) 4,041 (52.6%)
 Overweight (25.00–29.99 kg/m2) 2,435 (31.7%)
 Obesity (≥30.00 kg/m2) 929 (12.1%)
 Missing 676 (8.1%)
Diabetes mellitus (n, %) 523 (6.3%)
Heavy alcohol use (n, %)
 Ever 2,946 (35.3%)
 Never 5,207 (62.3%)
 No data on alcohol use available 201 (2.4%)
HIV transmission risk factors (n, %)
 Men who have sex with men 3,939 (47.2%)
 History of injection drug use 1,806 (21.6%)
 Receipt of blood transfusion, etc. 31 (0.4%)
 Heterosexual contact 842 (10.1%)
 Other 151 (1.8%)
 Unknown 2,020 (24.2%)
Chronic hepatitis C virus infection (n, %) 1,803 (21.6%)
HIV RNA (n, %)
 Median (log10 copies/mL, IQR) 2.6 (1.7–4.1)
 ≤500 copies/mL 4,567 (54.7%)
 >500 copies/mL 3,787 (45.3%)
Absolute CD4+ cell count (n, %)
 Median (cells/mm3, IQR) 354.0 (184.0–557.0)
 ≥500 cells/mm3 2,626 (31.4%)
 200–499 cells/mm3 3,450 (41.3%)
 <200 cells/mm3 2,278 (27.3%)
CD4+ cell percentage (n, %)
 Median (%, IQR) 21.0 (12.2–30.0)
 ≥28% 2,539 (30.4%)
 14–27.99% 3,454 (41.3%)
 <14% 2,361 (28.3%)
Platelet count (n, %)
 <150,000/μL 1,584 (19.0%)
 ≥150,000/μL 6,285 (75.2%)
 Not assessed at start of follow-up 485 (5.8%)
HBV DNA
 Median HBV DNA (log10 IU/mL, IQR) 2.0 (1.3–5.0)
 Quantitative HBV DNA (initial assessment during observation; n, %) 3,054 (36.6%)
  ≤200 IU/mL 1,688 (55.3%)
  201–2,000 IU/mL 215 (7.0%)
  >2,000 IU/mL 1,151 (37.7%)
 Assessed only for qualitative HBV DNA during observation (n, %) 2,307 (27.6%)
 Never assessed for quantitative or qualitative HBV DNA during observation (n, %) 2,993 (35.8%)
HBV e antigen (n, %)
 Negative 1,748 (20.9%)
 Positive 2,174 (26.0%)
 Never tested before or during follow-up 4,432 (53.1%)
On ART at start of follow-up (n, %) 6,702 (80.2%)
Anti-HBV ART regimen at start of follow-up (n, %) *
 Lamivudine or emtricitabine alone 3,997 (47.8%)
 Tenofovir disoproxil fumarate alone 142 (1.7%)
 Tenofovir disoproxil fumarate + (lamivudine or emtricitabine) 2,230 (26.7%)
 On ART, but no anti-HBV antiretroviral 333 (4.0%)
 Not on ART 1,652 (19.8%)
Year of start of follow-up (n, %)
 1995–2000 2,490 (29.8%)
 2001–2006 3,398 (40.7%)
 2007–2016 2,466 (29.5%)

Abbreviations: ART=antiretroviral therapy; HBV=hepatitis B virus; HIV=human immunodeficiency virus; IQR=interquartile range; RNA=ribonucleic acid

*

Results represent initial ART regimen.

Age was measured as year of baseline - year of birth.

Sex, race/ethnicity, and history of injection drug use were collected at enrollment into the NA-ACCORD.

History of heavy alcohol use was defined as ever having reported while under observation in the NA-ACCORD: 1) inpatient or outpatient diagnosis of alcohol dependence/abuse, or 2) ≥3 drinks/day or ≥7 drinks/week for females; ≥4 drinks/day or ≥14 drinks/week for males on the self-reported Alcohol Use Disorders Identification Test-Consumption questionnaire.

HIV transmission risk factors were not mutually exclusive.

Diabetes mellitus was defined by: 1) hemoglobin A1c ≥6.5%, 2) prescription of certain anti-diabetic medications, or 3) diabetes diagnosis plus prescription of certain anti-diabetic medications.

Chronic hepatitis C virus infection was defined by detectable HCV RNA or available HCV genotype recorded at any time during observation.

ART was measured as a combination of 3 antiretroviral agents from at least two classes or a triple nucleoside/nucleotide reverse transcriptase inhibitor regimen.