中华传染病杂志
中華傳染病雜誌
중화전염병잡지
CHINESE JOURNAL OF INFECTIOUS DISEASES
2013年
9期
533-537
,共5页
杨蓉蓉%桂希恩%熊勇%莫平征%高世成%荣玉萍%严亚军
楊蓉蓉%桂希恩%熊勇%莫平徵%高世成%榮玉萍%嚴亞軍
양용용%계희은%웅용%막평정%고세성%영옥평%엄아군
获得性免疫缺陷综合征%肝炎,乙型%抗反转录病毒治疗,高效
穫得性免疫缺陷綜閤徵%肝炎,乙型%抗反轉錄病毒治療,高效
획득성면역결함종합정%간염,을형%항반전록병독치료,고효
Acquired immunodeficiency syndrome%Hepatitis B%Antiretroviral therapy,highly active
目的 了解HBV感染对AIDS患者联合抗反转录病毒治疗(cART)效果的影响.方法 对HIV、HBV合并感染者78例和AIDS患者156例定期进行CD4+T淋巴细胞、HIV RNA、HBV血清学标志物和肝功能检测,并记录其生存情况,比较两组患者cART期间免疫学和病毒学应答的差异.计数资料采用卡方检验,计量资料采用t检验,非正态分布的计量资料采用两独立样本非参数检验.结果 cART第42个月时,同一治疗时间的CD4+T淋巴细胞和HIV RNA水平在HIV、HBV合并感染者与单纯AIDS患者间比较,差异均无统计学意义;cART第48、54和60个月时,HIV、HBV合并感染者免疫学和病毒学应答水平均低于单纯AIDS患者.HIV、HBV合并感染者在cART后第12、24、36、48和60个月时,13例患者中有3例在各时间点均表现为HBeAg阴转;抗-HBe阳转率分别为32.1%(9/28)、50.0%(14/28)、53.6%(15/28)、64.3%(18/28)和71.4%(20/28),阳转率逐年增高(x2=10.189,P=0.037); HBV DNA阴转率分别为95.1%(39/41)、82.9%(34/41)、68.3%(28/41)、43.9%(18/41)和43.9%(18/41),阴转率逐年下降(x2=29.982,P=0.000);肝功能异常率分别为32.1%(25/78)、51.4%(38/74)、33.8%(22/65)、47.9%(23/48)及6.7%(3/45),各时间点差异有统计学意义(x2=28.053,P=0.000).HIV、HBV合并感染者及单纯AIDS患者的病死率分别为24.4%(19/78)和5.1%(8/156),差异有统计学意义(x2=18.841,P<0.01),且HIV、HBV合并感染者84.2%死于HBV相关的终末期肝病.结论 合并HBV感染可影响cART的远期疗效,终末期肝病是HIV、HBV合并感染者接受cART后的首要死因.
目的 瞭解HBV感染對AIDS患者聯閤抗反轉錄病毒治療(cART)效果的影響.方法 對HIV、HBV閤併感染者78例和AIDS患者156例定期進行CD4+T淋巴細胞、HIV RNA、HBV血清學標誌物和肝功能檢測,併記錄其生存情況,比較兩組患者cART期間免疫學和病毒學應答的差異.計數資料採用卡方檢驗,計量資料採用t檢驗,非正態分佈的計量資料採用兩獨立樣本非參數檢驗.結果 cART第42箇月時,同一治療時間的CD4+T淋巴細胞和HIV RNA水平在HIV、HBV閤併感染者與單純AIDS患者間比較,差異均無統計學意義;cART第48、54和60箇月時,HIV、HBV閤併感染者免疫學和病毒學應答水平均低于單純AIDS患者.HIV、HBV閤併感染者在cART後第12、24、36、48和60箇月時,13例患者中有3例在各時間點均錶現為HBeAg陰轉;抗-HBe暘轉率分彆為32.1%(9/28)、50.0%(14/28)、53.6%(15/28)、64.3%(18/28)和71.4%(20/28),暘轉率逐年增高(x2=10.189,P=0.037); HBV DNA陰轉率分彆為95.1%(39/41)、82.9%(34/41)、68.3%(28/41)、43.9%(18/41)和43.9%(18/41),陰轉率逐年下降(x2=29.982,P=0.000);肝功能異常率分彆為32.1%(25/78)、51.4%(38/74)、33.8%(22/65)、47.9%(23/48)及6.7%(3/45),各時間點差異有統計學意義(x2=28.053,P=0.000).HIV、HBV閤併感染者及單純AIDS患者的病死率分彆為24.4%(19/78)和5.1%(8/156),差異有統計學意義(x2=18.841,P<0.01),且HIV、HBV閤併感染者84.2%死于HBV相關的終末期肝病.結論 閤併HBV感染可影響cART的遠期療效,終末期肝病是HIV、HBV閤併感染者接受cART後的首要死因.
목적 료해HBV감염대AIDS환자연합항반전록병독치료(cART)효과적영향.방법 대HIV、HBV합병감염자78례화AIDS환자156례정기진행CD4+T림파세포、HIV RNA、HBV혈청학표지물화간공능검측,병기록기생존정황,비교량조환자cART기간면역학화병독학응답적차이.계수자료채용잡방검험,계량자료채용t검험,비정태분포적계량자료채용량독립양본비삼수검험.결과 cART제42개월시,동일치료시간적CD4+T림파세포화HIV RNA수평재HIV、HBV합병감염자여단순AIDS환자간비교,차이균무통계학의의;cART제48、54화60개월시,HIV、HBV합병감염자면역학화병독학응답수평균저우단순AIDS환자.HIV、HBV합병감염자재cART후제12、24、36、48화60개월시,13례환자중유3례재각시간점균표현위HBeAg음전;항-HBe양전솔분별위32.1%(9/28)、50.0%(14/28)、53.6%(15/28)、64.3%(18/28)화71.4%(20/28),양전솔축년증고(x2=10.189,P=0.037); HBV DNA음전솔분별위95.1%(39/41)、82.9%(34/41)、68.3%(28/41)、43.9%(18/41)화43.9%(18/41),음전솔축년하강(x2=29.982,P=0.000);간공능이상솔분별위32.1%(25/78)、51.4%(38/74)、33.8%(22/65)、47.9%(23/48)급6.7%(3/45),각시간점차이유통계학의의(x2=28.053,P=0.000).HIV、HBV합병감염자급단순AIDS환자적병사솔분별위24.4%(19/78)화5.1%(8/156),차이유통계학의의(x2=18.841,P<0.01),차HIV、HBV합병감염자84.2%사우HBV상관적종말기간병.결론 합병HBV감염가영향cART적원기료효,종말기간병시HIV、HBV합병감염자접수cART후적수요사인.
Objective To investigate the influence of hepatitis B virus (HBV) infection on efficacy of combined antiretroviral therapy (cART) in patients with acquired immunodeficiency syndrome (AIDS).Methods Seventy-eight subjects with human immunodeficiency virus (HIV)/HBV co-infection and 156 subjects with HIV mono-infection were included.CD4+ T cell count,HIV viral load,HBV-markers and liver functions were routinely tested.The differences in survival rate,as well as immunological and virological responses between the two groups (HIV/HBV co-infection group and HIV mono-infection group) during cART were compared.Categorical data were compared by Chisquare test,measurement data were compared by t test,and measurement data with abnormal distribution were compared by Mann-Whitney test.Results At month 42 of cART,HIV RNA levels and CD4+ T cell counts of the two groups were comparable.However,at month 48,54 and 60 of cART,the immunological and virological responses of HIV/HBV co-infection group were less favorable than those of HIV mono-infection group.At each time point of month 12,24,36,48 and 60 of cART,3 out of 13 subjects with HIV/HBV co-infection maintained hepatitis B e antigen (HBeAg)loss; the HBeAg seroconversion rates were 32.1% (9/28),50.0% (14/28),53.6% (15/28),64.3% (18/28) and 71.4% (20/28),respectively (x2 =10.189,P=0.037) ; HBV DNA negative rates were 95.1% (39/41),82.9% (34/41),68.3% (28/41),43.9% (18/41) and 43.9% (18/41),respectively (x2 =29.982,P=0.000); liver dysfunction rate was 32.1 % (25/78),51.4% (38/74),33.8% (22/65),47.9% (23/48) and 6.7% (3/45),respectively (x2 =28.053,P=0.000).Mortalities in HIV/HBV co-infected and HIV mono-infected individuals were 24.4% (19/78) and 5.1 % (8/156),respectively (x2 =18.841,P<0.01).Sixteen out of the 19 deaths (84.2 %) in HIV/ HBV co-infected subjects died of end stage liver diseases.Conclusions HBV co-infection diminishes the long term efficacy of cART.End stage liver diseases are the primary cause of death in HIV/HBV co-infected subjects during cART.