Brand Martin, Woodiwiss Angela J, Michel Frederic, Nayler Simon, Veller Martin G, Norton Gavin R
Department of Surgery, School of Medicine, University of the Witwatersrand, Johannesburg, South Africa.
Cardiovascular Pathophysiology and Genomics Research Unit, School of Physiology, University of the Witwatersrand, Johannesburg, South Africa.
PLoS One. 2014 Aug 29;9(8):e106205. doi: 10.1371/journal.pone.0106205. eCollection 2014.
Whether a human immunodeficiency virus (HIV)-associated vasculitis in-part accounts for occlusive large artery disease remains uncertain. We aimed to identify the histopathological features that characterize large vessel changes in HIV sero-positive as compared to sero-negative patients with critical lower limb ischemia (CLI).
Femoral arteries obtained from 10 HIV positive and 10 HIV negative black African male patients admitted to a single vascular unit with CLI requiring above knee amputation were subjected to histopathological assessment. None of the HIV positive patients were receiving antiretroviral therapy.
As compared to HIV negative patients with CLI, HIV positive patients were younger (p<0.01) and had a lower prevalence of hypertension (10 vs 90%, p<0.005) and diabetes mellitus (0 vs 50%, p<0.05), but a similar proportion of patients previously or currently smoked (80 vs 60%). 90% of HIV positive patients, but no HIV negative patient had evidence of adventitial leukocytoclastic vasculitis of the vasa vasorum (p<0.0001). In addition, 70% of HIV positive, but no HIV negative patient had evidence of adventitial slit-like vessels. Whilst T-lymphocytes were noted in the adventitia in 80% of HIV positive patients, T-lymphocytes were noted only in the intima in HIV negative patients. The presence of femoral artery calcified multilayered fibro-atheroma was noted in 40% of HIV positive and 90% of HIV negative patients with CLI.
An adventitial vasculitis which characterizes large artery changes in CLI in HIV-infected as compared to non-infected patients, may contribute toward HIV-associated occlusive large artery disease.
人类免疫缺陷病毒(HIV)相关血管炎在一定程度上是否导致闭塞性大动脉疾病仍不确定。我们旨在确定与患有严重下肢缺血(CLI)的HIV血清阴性患者相比,HIV血清阳性患者大血管病变的组织病理学特征。
对来自单一血管科、因CLI需要进行膝上截肢的10名HIV阳性和10名HIV阴性的非洲黑人男性患者的股动脉进行组织病理学评估。所有HIV阳性患者均未接受抗逆转录病毒治疗。
与患有CLI的HIV阴性患者相比,HIV阳性患者更年轻(p<0.01),高血压患病率更低(10%对90%,p<0.005),糖尿病患病率更低(0对50%,p<0.05),但既往或当前吸烟的患者比例相似(80%对60%)。90%的HIV阳性患者有血管滋养管外膜白细胞破碎性血管炎的证据,而HIV阴性患者均无此证据(p<0.0001)。此外,70%的HIV阳性患者有外膜裂隙样血管的证据,而HIV阴性患者均无。80%的HIV阳性患者外膜有T淋巴细胞,而HIV阴性患者仅在内膜有T淋巴细胞。40%的HIV阳性CLI患者和90%的HIV阴性CLI患者存在股动脉钙化多层纤维粥样瘤。
与未感染患者相比,HIV感染患者CLI中大动脉病变特征性的外膜血管炎可能导致HIV相关的闭塞性大动脉疾病。