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. 2014 Mar 5;58(11):1625–1633. doi: 10.1093/cid/ciu127

Table 1.

Clinical Characteristics of Hepatitis D Virus–Seropositive and –Seronegative Subjects

Characteristic Seropositive for HDV IgG Seronegative for HDV IgG P Value
No. of subjects 38 337
Age, y, mean (SD) 38 (7) 40 (10) .03
Male sex, % (No.) 94.7 (36) 97.0 (327) .45
CD4, cells/µL, mean (SD) 581 (293) 479 (277) .20
CD4 count <200 cells/µL, % (No.) 7.9 (3/38) 14.7 (49/333) .25
Plasma HIV RNA, log10 copies/mL, mean (SD) 2.00 (1.23) 2.29 (1.19) .25
Plasma HIV RNA <400 copies/mL, % (No.) 63.2 (24/38) 75.0 (252/336) .12
Risk behavior, % (No.)
 MSM 50.0 (19) 70.6 (238) .02
 Heterosexual 7.9 (3) 13.7 (46) .47
 IDU 39.5 (15) 5.6 (19) <.001
 Others 2.6 (1) 10.0 (34) .21
Receipt of cART, % (No.) 68.4 (26/38) 87.7 (292/333) .001
Receipt of lamivudine, % (No.) 68.4 (26/38) 87.7 (292/333) .001
Receipt of TDF, % (No.) 23.7 (9/38) 31.7 (105/331) .31
Anti-HCV positive, % (No.) 39.5 (15/38) 10.6 (34/320) <.001
Plasma HBV DNA, log10 copies/mL, mean (SD) 2.21 (1.22) 2.71 (1.89) .03
Total bilirubin, mg/dL, mean (SD) 1.43 (1.15) 1.23 (1.10) .08
Bilirubin level ≥1.2 mg/dL, % (No.) 47.6 (10/21) 34.0 (53/156) .22
AST, U/L, mean (SD) 51.8 (87.4) 45.0 (138.7) .24
AST level ≥37 U/L, % (No.) 60.0 (15/25) 26.7 (60/225) .001
ALT, U/L, mean (SD) 57.7 (98.6) 52.4 (140.4) .31
ALT level ≥41 U/L, % (No.) 64.5 (20/31) 29.7 (66/222) <.001
ALP, U/L, mean (SD) 173.3 (136.8) 176.3 (184.2) .89
Recent syphilisa, % (No.) 13.0 (3/23) 5.6 (16/286) .15
RPR ≥32, % (No.) 8.8 (3/34) 4.8 (15/318) .30

Abbreviations: ALP, alkaline phosphatase; ALT, alanine aminotransferase; AST, aspartate aminotransferase; cART, combination antiretroviral therapy; HBV, hepatitis B virus; HCV, hepatitis C virus; HDV, hepatitis D virus; HIV, human immunodeficiency virus; IDU, injection drug use; IgG, immunoglobulin G; MSM, men who have sex with men; RPR, rapid plasma reagin; SD, standard deviation; TDF, tenofovir disoproxil fumarate.

a Recent syphilis was defined as having new RPR seroreactivity or a 4-fold increase in RPR titers within the 6 months of HDV seroconversion or within the 6 months of the last anti-HDV testing.