CARDIOVASCULAR JOURNAL OF AFRICA • Volume 26, No 2, March/April 2015
70
AFRICA
Review Article
HIV-associated large-vessel vasculopathy: a review of
the current and emerging clinicopathological spectrum
in vascular surgical practice
Balasoobramanien Pillay, Pratistadevi K Ramdial, Datshana P Naidoo
Abstract
An established relationship exists between human immunode-
ficiency virus (HIV) and the vascular system, which is char-
acterised by clinical expressions of aneurysmal and occlusive
disease that emanate from a common pathological process.
The exact pathogenesis is currently unknown; attempts to
implicate opportunistic pathogens have been futile. Theories
converge on leucocytoclastic vasculitis with the vaso vasora as
the vasculopathic epicentre. It is thought that the virus itself
or viral proteins trigger the release of inflammatory media-
tors that cause endothelial dysfunction and smooth muscle
proliferation leading to vascular injury and thrombosis.
The beneficial effects of highly active anti-retroviral therapy
alter the natural history of the disease profile and promote
longevity but are negated by cardiovascular complications.
Atherosclerosis is an emerging challenge. Presently patients
are managed by standard surgical protocols because of non-
existent universal surgical interventional guidelines. Clinical
response to treatment is variable and often compounded by
complications of graft occlusion, sepsis and poor wound
healing. The clinical, imaging and pathological observations
position HIV-associated large-vessel vasculopathy as a unique
entity. This review highlights the spectrum of HIV-associated
large-vessel aneurysmal, occlusive and atherosclerotic disease
in vascular surgical practice.
Keywords:
human immunodeficiency virus, vasculopathy, aneu-
rysms, occlusive disease, atherosclerosis, vascular surgery
Submitted 3/7/14, accepted 27/1/15
Cardiovasc J Afr
2015;
26
: 70–81
www.cvja.co.zaDOI: 10.5830/CVJA-2015-017
Since the first description of human immunodeficiency virus
(HIV) disease more than three decades ago,
1
HIV infection
has become a global phenomenon, afflicting approximately 40
million people worldwide.
2
Over 70% of infected individuals
reside in sub-Saharan Africa.
2
HIV is implicated in a multisystem disease process and the
cardiovascular system is not spared. Many infected patients
are in the advanced stages of disease and present with vascular
complications.
3,4
The unique vascular manifestations of
HIV-related disease, documented as early as 1987 in children,
5
may present with a diverse spectrum of aneurysms, occlusive
disease, spontaneous arteriovenous fistulae and dissections. In
addition, despite the heightened recognition of the spectrum
of HIV and other HIV-associated infective vasculitic and
vasculopathic reactions,
6-10
the exact pathogenetic mechanisms
and reasons underpinning the varied manifestations of the
HIV-associated vascular pathology remain enigmatic.
This review discusses the spectrum of HIV-associated
large-vessel disease in vascular surgical practice, including
the current understanding of pathogenetic mechanisms, the
clinicopathological profile of aneurymal and occlusive disease,
and the impact of highly active anti-retroviral therapy (HAART)
in the development of atherosclerosis in this patient population.
Pathogenesis of HIV-associated large-vessel
vasculopathy
The pathogenesis of HIV-associated large vessel vasculopathy
involves intricate, dynamic interactions between viral-induced
inflammatory responses, vascular smooth muscle changes,
endothelial alterations and circulating blood factors that result
in pathological vessel wall alterations and symptomatic clinical
disease (Fig. 1A, B).
11,12
Inflammatory alterations
The hallmark pathological feature common to aneurysmal and
occlusive disease is an HIV-associated vasculitic process, the
exact mechanism of which is poorly understood (Fig. 1A, B).
13,14
Department of Vascular/Endovascular Surgery, Nelson R
Mandela School of Medicine, Durban, South Africa
Balasoobramanien Pillay, BSc, BSc (Hons), MB ChB, FCS (SA),
CVS (SA),
balapil@ialch.co.za;
balapillay@vodamail.co.zaDepartment of Anatomical Pathology, School of Laboratory
Medicine and Medical Sciences, University of KwaZulu-
Natal and National Health Laboratory Service, Durban,
South Africa
Pratistadevi K Ramdial, FCPath (Anat) (SA)
Department of Cardiology, University of KwaZulu-Natal,
Durban, South Africa
Datshana P Naidoo, FRCP (SA)