Encyclopedia
Please note this is a comparison between Version 1 by Flavius-Alexandru Gherasie and Version 2 by Rita Xu.
There are a number of devastating complications associated with peripheral artery disease, including limb amputations and acute limb ischemia. In coronary atherosclerosis, thrombosis is often precipitated by rupture or erosion of fibrous caps around atheromatous plaques, which leads to acute coronary syndrome.
- peripheral artery disease
- chronic limb-threatening ischemia
- acute limb ischemia
1. Introduction
More than 200 million adults suffer from peripheral artery disease in their lower extremities, which increases their risk of cardiovascular events (such as coronary heart disease, strokes, and leg amputations). Globally and in the United States, peripheral artery disease has gone underdiagnosed and undertreated due to a lack of awareness [1]. Generally speaking, lower-extremity peripheral artery disease refers to atherosclerotic diseases of the arteries supplying the limbs, from the aortoiliac segments to the pedal arteries. Even though this disease is associated with adverse clinical outcomes, impaired physical function, and reduced physical activity, it has been understudied and underrecognized compared with other atherosclerotic diseases such as myocardial infarction. In recent years, there has been mounting evidence that peripheral artery disease is significantly linked to mortality, primarily as a risk factor for future myocardial infarctions and strokes. Also, peripheral artery disease can cause devastating complications that result in limb amputations and acute limb ischemia. Despite the overlap, the causes of atherosclerotic diseases are not the same and the need for the appropriate diagnosis and treatment remains a major concern for medicine. Clinically, peripheral artery disease and coronary artery disease overlap due to their shared risk factors. In these patients, hyperlipidemia and type II diabetes mellitus were significant comorbidities. In addition to accelerating atherosclerosis development, diabetes mellitus affects the characteristic of atherosclerotic lesions in the lower extremities [2][3][2,3]. Compared with patients with PAD (peripheral artery disease) and without diabetes mellitus, patients who have PAD and coexisting diabetes mellitus have more arteries below the knee that are affected and more multilevel lesions [4][5][6][4,5,6]. Although patients with diabetes mellitus benefit from medical and endovascular procedures to manage atherosclerotic cardiovascular diseases, restenosis is a significant factor that may worsen the prognosis and may be associated with the necessity of reintervention [7]. The presence of dyslipidemia is associated with both changes in basic lipid parameters and modified lipoproteins, which are not routinely measured in clinical practice. Nitrated lipoproteins are oxidatively modified lipoproteins discussed in the context of cardiovascular dysfunction development. However, their role remains unclear at this time [8]. Many studies have found that coronary artery disease and peripheral artery disease are frequently coexisting conditions. Saleh et al. suggested that there was a significant increase in peripheral artery disease prevalence among those with coronary artery disease compared with those with normal coronaries [9]. Despite being under the care of a cardiovascular specialist, studies have shown that one out of six patients with coronary artery disease had an unrecognized peripheral artery disease [10].
The ankle-brachial index’s high positive predictive value and the high prevalence of peripheral artery disease with coronary artery disease suggest a high degree of suspicion for, and pretest probability for, coronary artery disease in a patient with peripheral artery disease. Coronary artery disease diagnosis is highly dependent on cardiac imaging tests such as electrocardiograms, stress electrocardiograms, myocardial perfusion imaging, and coronary angiographies. Kumar et al. say pretest probabilities can be increased through the ankle-brachial index, but it cannot replace the above testing methods [11].
Many factors contribute to this lack of knowledge about peripheral artery disease. Various nomenclatures and definitions have been used to describe peripheral artery disease, making effective communication challenging [12]. It is also likely that the clinical presentation of peripheral artery disease contributes to confusion regarding peripheral artery disease. A small percentage of patients are diagnosed with intermittent claudication, with either no exertional leg symptoms (up to 50%) or atypical leg symptoms (almost 50%) [13]. Patients may experience leg pain that begins at rest, or that does not interfere with walking, or that resolves with rest. These symptoms can be confused with arthritis or degenerative spinal disease. Various adverse outcomes can occur as a result of peripheral artery disease. To improve overall outcomes among this growing and undertreated population, increasing awareness about the definition, diagnosis, clinical manifestations, and complications of peripheral artery disease is critical.
Coronary atherosclerosis often manifests as an acute coronary syndrome, where thrombosis is precipitated by rupture or erosion of the fibrous caps of atheromatous plaques. It is common for plaque ruptures to have large necrotic cores, as well as thin, inflamed fibrous caps. Regardless of the extent of atherosclerosis, peripheral artery disease manifests as thrombosis. In peripheral arteries with significant stenosis, approximately 75% of them are blocked by thrombi. Two-thirds of them also have thrombi associated with insignificant atherosclerosis. A local thrombogenic or remotely embolic basis of critical limb ischemia may be explained by obliterative thrombi in peripheral arteries of patients without coronary artery-like lesions [14].
2. Anatomy of Lower Extremity Arteries: Normal Aspects
To maintain the body’s mobility, lower extremity arteries supply oxygenated blood to muscles, tendons, and nerves. Several diseases can affect these arteries, which inhibit the optimal function of the limb. Lower-extremity arteries originate from the iliac artery at the point where the abdominal aorta is divided into the two common iliac arteries and the median sacral artery, approximately at the fourth lumbar vertebral body [15][16][25,26]. There are two branches of the common iliac artery, the internal and the external. A portion of the external iliac artery runs down into the lower limbs and becomes the common femoral artery [17][27]. Among the small branches of the common femoral artery, there are the superficial epigastric artery, external pudendal artery, and superficial circumflex artery. The common femoral artery divides into the superficial and deep femoral arteries. Through Hunter’s canal, the superficial femoral artery travels along the medial side of the thigh. Once it exits the adductor canal, the superficial femoral artery courses posteriorly, where it is called the popliteal artery after it passes through the adductor hiatus. Approximately at the level of the proximal tibiofibular joint, the popliteal artery divides into the anterior tibial artery and the tibioperoneal trunk [18][28]. The anterior tibial artery runs along the anterior surface of the interosseus membrane, and there is a continuation of this artery in the foot as the dorsalis pedis artery. Located along the posteromedial aspect of the leg, the tibioperoneal trunk further divides into the peroneal artery and posterior tibial artery [15][25]. There are two arches on the medial and lateral surfaces of the plantar surface, formed by the posterior tibial artery. Besides giving rise to the metatarsals, the plantar arch is also responsible for producing the plantar digital arteries. Above the ankle joint, the peroneal artery divides into two calcaneal branches, one on the medial side and one on the lateral side. As a result of free communication with the dorsalis pedis artery and posterior tibial artery, these branches assist in the collateralization of the foot when it is sick or injured [19][29].3. Atherosclerosis
Atherosclerosis is a chronic inflammatory disease with complex etiopathogenesis, which results in the development of atherosclerotic plaques, leading to the formation of narrowing and/or occlusion of the arteries [20][21][30,31]. This clinically may lead to the development of ischemic heart disease, cerebrovascular disease, or peripheral arterial disease [22][23][24][25][32,33,34,35]. In clinical practice, lowering the level of LDL cholesterol (low-density lipoprotein cholesterol) is the primary therapeutic objective of lipid-lowering therapy due to the role that oxidatively modified LDL particles play in atherosclerosis [26][27][28][36,37,38]. Additionally, reswearchers observe patients with advanced atherosclerosis and normal LDL concentrations in clinical practice, and such patients are also eligible for statin therapy. There are many pleiotropic effects associated with statins, which are mainly used for lowering cholesterol, and thus they are not only lipid-lowering drugs [27][37]. To achieve a target level for LDL cholesterol, statins and PCSK9 inhibitors (proprotein convertase subtilisin/kexin type 9) are effective [29][30][31][39,40,41]. There is no doubt that both of them are effective in controlling LDL cholesterol and reducing major adverse cardiovascular events by about 50% [32][42]. After controlling LDL cholesterol, the remaining risk for major adverse cardiovascular events is believed to be due to inflammation. As part of the CANTOS trial, it was shown that canakinumab, an antibody that blocks IL-1β (interleukin-1β), reduces major adverse cardiovascular events [33][34][35][35][36][37][43,44,45,45,46,47]. As a result of atherosclerosis, there is an autoimmune response to LDL and other antigens which could lead to an escalation or amelioration of the disease’s progression. There have been some recent advances in immunotherapy and vaccination that have shown promise in curbing atherosclerosis in animal models [38][48]. Based on the theory of the modulation of atherogenesis by adaptive immune responses, especially the CD4+ T cells that recognize self-antigens, a novel type of therapy that targets the adaptive immune response has been developed to address this phenomenon [39][49].3.1. Pathogenesis of Atherosclerosis
Early-stage atherosclerosis is characterized by cell formation which is the result of lipid accumulation in the cells [40][41][42][50,51,52]. Inflammatory cytokines are released by damaged endothelial cells, which recruit monocytes through the endothelium and then differentiate into macrophages. Differentiated macrophages consume oxidized low-density lipoprotein (ox-LDL) through the scavenger receptors LOX-1, CD36, and SR-A1, which hydrolyze cholesteryl esters within lysosomes. By contrast, free cholesterol is esterified by acyl-CoA cholesterol acyltransferase 1 (ACAT1), while cholesteryl ester is hydrolyzed by neutral cholesteryl ester hydrolase (nCEH) and cholesteryl ester hydrolase (CEH) [41][43][51,53]. A large amount of free cholesterol is toxic to cells, so it must be efficiently removed from cells by ABCA1 and ABCG1 transporters [44][45][54,55]. When the above cholesterol homeostasis is disturbed, excessive cholesterol ester or free cholesterol will accumulate, causing foam cell formation or cell necrosis.3.2. Immune Response in Atherosclerosis
Atherosclerotic plaques can become unstable, rupture, or erode over time, causing major cardiovascular complications [45][46][47][48][49][55,56,57,58,59]. There is a direct correlation between plaque stability and the level of inflammatory cells as well as the thickness of the cap of the plaque. Plaques that have thin caps and are full of immune cells are referred to as soft or vulnerable plaques. To initiate immune cell infiltration, chemokines and adhesion molecules play a major role. An antigen-presenting cell is a cell that generates major histocompatibility complex molecules, costimulatory molecules, and cytokines upon the presence of antigens that are produced by pathogens, bacteria, or altered self to determine the polarization of the adaptive immune response. In the arterial adventitia and neointima, there are macrophages and dendritic cells that are activated by TLR ligands (Toll-like receptors) and scavenger receptors [50][60]. As inflammation cytokines increase in amount and intensity, atherosclerosis gets worse, and more immune cells are attracted to the area. The inflammatory cytokine IL-1β is an effective target for the treatment of atherosclerosis and other vascular diseases [48][58]. Marchini et al. suggested that at the maturation stage of atherosclerotic plaque, atherosclerosis-antigen-specific T cells release cytokines, perpetuate inflammation, and help an immune cell infiltrate develop over time [51][61] (Figure 1).
Figure 1. Adaptive immune responses in atherosclerosis. LDL penetrates the artery wall and experiences modification by oxidative and enzymatic processes. The modified LDL molecules promote the expression of leukocyte adhesion molecules. Monocytes invade the vascular wall and mature into macrophages, differentiating into foam cells after taking up large volumes of oxidized LDL. T cells become active throughout this process and release mediators, which subsequently increase the immune reaction and lead to atherogenesis. LDL, low-density lipoprotein; oxLDL, oxidized low-density lipoprotein.
