Marin Benoît, Thiébaut Rodolphe, Bucher Heiner C, Rondeau Virginie, Costagliola Dominique, Dorrucci Maria, Hamouda Osamah, Prins Maria, Walker Sarah, Porter Kholoud, Sabin Caroline, Chêne Geneviève
INSERM, U897, Bordeaux, France
AIDS. 2009 Aug 24;23(13):1743-53. doi: 10.1097/QAD.0b013e32832e9b78.
To assess whether immunodeficiency is associated with the most frequent non-AIDS-defining causes of death in the era of combination antiretroviral therapy (cART).
Observational multicentre cohorts.
Twenty-three cohorts of adults with estimated dates of human immunodeficiency virus (HIV) seroconversion were considered. Patients were seroconverters followed within the cART era. Measurements were latest CD4, nadir CD4 and time spent with CD4 cell count less than 350 cells/microl. Outcomes were specific causes of death using a standardized classification.
Among 9858 patients (71 230 person-years follow-up), 597 died, 333 (55.7%) from non-AIDS-defining causes. Non-AIDS-defining infection, liver disease, non-AIDS-defining malignancy and cardiovascular disease accounted for 53% of non-AIDS deaths. For each 100 cells/microl increment in the latest CD4 cell count, we found a 64% (95% confidence interval 58-69%) reduction in risk of death from AIDS-defining causes and significant reductions in death from non-AIDS infections (32, 18-44%), end-stage liver disease (33, 18-46%) and non-AIDS malignancies (34, 21-45%). Non-AIDS-defining causes of death were also associated with nadir CD4 while being cART-naive or duration of exposure to immunosuppression. No relationship between risk of death from cardiovascular disease and CD4 cell count was found though there was a raised risk associated with elevated HIV RNA.
In the cART era, the most frequent non-AIDS-defining causes of death are associated with immunodeficiency, only cardiovascular disease was associated with high viral replication. Avoiding profound and mild immunodeficiency, through earlier initiation of cART, may impact on morbidity and mortality of HIV-infected patients.
评估在联合抗逆转录病毒疗法(cART)时代,免疫缺陷是否与最常见的非艾滋病定义性死亡原因相关。
观察性多中心队列研究。
纳入23个队列的成人,这些队列有估计的人类免疫缺陷病毒(HIV)血清转换日期。患者为在cART时代随访的血清转换者。测量指标为最新CD4细胞计数、最低CD4细胞计数以及CD4细胞计数低于350个/微升的时间。结局为使用标准化分类的特定死亡原因。
在9858例患者(71230人年随访)中,597例死亡,333例(55.7%)死于非艾滋病定义性原因。非艾滋病定义性感染、肝病、非艾滋病定义性恶性肿瘤和心血管疾病占非艾滋病死亡的53%。最新CD4细胞计数每增加100个/微升,我们发现艾滋病定义性原因导致的死亡风险降低64%(95%置信区间58 - 69%),非艾滋病感染导致的死亡显著降低(32%,18 - 44%),终末期肝病导致的死亡显著降低(33%,18 - 46%),非艾滋病恶性肿瘤导致的死亡显著降低(34%,21 - 45%)。非艾滋病定义性死亡原因也与最低CD4细胞计数相关,同时与未接受cART或免疫抑制暴露持续时间有关。未发现心血管疾病导致的死亡风险与CD4细胞计数之间的关系,尽管与HIV RNA升高相关的风险有所增加。
在cART时代,最常见的非艾滋病定义性死亡原因与免疫缺陷相关,只有心血管疾病与高病毒复制相关。通过更早开始cART避免严重和轻度免疫缺陷,可能会影响HIV感染患者的发病率和死亡率。