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20 January 2022: Review Articles  

Impact of Arterial Hypertension on the Eye: A Review of the Pathogenesis, Diagnostic Methods, and Treatment of Hypertensive Retinopathy

Jacek Dziedziak1EF, Anna Zaleska-Żmijewska2DEF, Jacek Paweł Szaflik2DEF, Agnieszka Cudnoch-Jędrzejewska1ADEF*

DOI: 10.12659/MSM.935135

Med Sci Monit 2022; 28:e935135




ABSTRACT: The number of patients with arterial hypertension is continually increasing. Hypertension can cause organ complications, called hypertension-mediated organ damage (HMOD). One example is hypertensive retinopathy, in which high blood pressure (BP) damages both the retinal microcirculation and the retinal nerve fiber layer (RNFL). This can result in progressive and painless vision deterioration in some groups of patients. Unlike anywhere else in the human body, the microvasculature of the retina can be observed in vivo, and the progression of changes can be closely monitored. The harmful effect of increased BP on the eye is not only limited to hypertensive retinopathy, but can also lead to an exacerbation of diabetic retinopathy (DR) and to an increase in intraocular pressure (IOP), and it can also trigger the formation of thromboembolic lesions. This review presents an update on the pathogenesis of hypertensive retinopathy and the use of adaptive optics (AO) combined with optical coherence tomography (OCT) to evaluate the retinal microvasculature. The latest progress and directions of research in the field of hypertensive retinopathy are also discussed.

Keywords: Neovascularization, Pathologic, Hypertensive retinopathy, Hypertension, Retinal Neovascularization, Angiotensin-Converting Enzyme Inhibitors, Antihypertensive Agents, Humans, Tomography, Optical Coherence


Hypertension can be diagnosed when systolic blood pressure (SBP) exceeds 140 mmHg and/or when diastolic blood pressure (DBP) is over 90 mmHg [1]. These criteria apply to the adult population. In children and adolescents, blood pressure (BP) norms are expressed on percentile charts, and average SBP and DBP should not exceed the 95th percentile [2]. Hypertension is a severe epidemiological problem. Currently, the number of people with hypertension exceeds 1.4 billion [3] and hypertension is responsible for more than 10 million deaths per year [4]. The number of patients is estimated to exceed 1.5 billion in 2025 [5]. Despite increasingly effective pharmacotherapy and a greater awareness of hypertension and its complications, this condition is still particularly dangerous [6]. For many years, it can proceed asymptomatically or it can display non-specific symptoms and is often diagnosed incidentally [7]. There are several organ complications, collectively referred to as hypertension-mediated organ damage (HMOD) in the course of vascular lesions that accompany hypertension, such as vascular endothelial damage, remodeling of small and large arteries, and vascular rarefaction [8]. This name (HMOD) has replaced the previously used term, target organ damage (TOD). HMOD includes ischemic and hemorrhagic stroke; coronary heart disease (CHD) with myocardial infarction (MI), proteinuria, and renal failure; and retinopathy and atherosclerotic changes, including the development of stenoses and aneurysms [9]. If hypertension remains untreated, or if it is diagnosed late, or if it is not controlled sufficiently, then the risk of developing HMOD increases [10].

Hypertensive retinopathy is an example of HMOD, which is caused by several vascular changes in the retinal microcirculation [11]. Signs of hypertensive retinopathy can be detected in 6–15% of the non-diabetic population aged 40 years and older [6], but this number is thought to be significantly underestimated [12]. It was first described by Marcus Gunn in the late 19th century, and the first classification of changes visible on the fundus of the eye was created by Keith, Wagener, and Barker (KWB) in the late 1930s [13]. This classification distinguishes the 4 stages of severity of the lesions: grade I – generalized retinal arteriolar narrowing; grade II – arteriovenous (AV) crossing and more severe generalized and focal areas of arteriolar narrowing; grade III – grade I and II with the additional presence of exudates and hemorrhages; and grade IV – papilledema, also called malignant hypertensive retinopathy [13]. To this day, this classification is widely used, despite its numerous limitations, including poor clinical and prognostic value (the most frequent are early findings of non-specific retinal alterations such as diffuse or focal arteriolar narrowing) and considerable interobserver and intraobserver variability [14]. There were several attempts made to modify the KWB classification. One of them was the classification proposed by Mitchell and Wong. This classification combined grades I and II of KWB classification into mild-grade hypertensive retinopathy, and distinguished moderate and malignant stages, which corresponded to grade III and IV of the KWB classification, respectively. Unfortunately, it did not meet expectations and only simplified clinical practice [15,16]. Lesions characteristic for advanced retinopathy have been proven to have a predictive value for HMOD [17]. It is increasingly suggested that less advanced changes are also important [18]. The fact that retinal vessels are terminal vessels and are highly susceptible to changes in BP may reflect the vasculature condition of the entire organism [19]. In addition, the development of hypertensive retinopathy can lead to a gradual, painless deterioration of vision and it can cause blindness as it progresses [20].

The aim of this review is to summarize current views on the pathophysiology, diagnostics, therapy, and predictive value of hypertensive retinopathy and to introduce novel and promising research directions in this field. Therefore, this review presents an update on the pathogenesis of hypertensive retinopathy and the use of AO combined with OCT to evaluate the retinal microvasculature.

Retinal Vasculature

Retinal vasculature is mainly derived from the central retinal artery (CRA), the first intraorbital branch of the ophthalmic artery. The CRA penetrates the optic nerve, and then enters the eye through the central part of the optic disc, where it is divided into 2 main branches. These branches divide further into arterioles which supply the peripheral parts of the retina. Each arteriole provides the vascularity of the inner nerve layer of 1 quadrant of the retina. The CRA is the terminal vessel, and when it is occluded, sudden blindness occurs [21,22]. Larger vessels lie in the inner part of the retina, near the inner limiting membrane. Arterioles form 2 layers of capillaries: the superficial vascular plexus (SVP) located in the nerve fiber and the ganglion cell layer; and the deep capillary plexus (DCP) which lies deeper in the inner nuclear layer. The development of optical coherence tomography angiography (OCTA) helped to better understand the complexity of retinal vasculature, whose vessels are only 100–300 μm in diameter [23]. In addition, the intermediate capillary plexus (ICP), which lies between the SVP and the DCP, and the radial peripapillary capillary plexus (RPCP), which supplies the nerve fiber layer (NFL) bundles, have been identified [22,24,25]. The retinal pigment epithelium (RPE) and the outer retina are nourished by diffusion from the choriocapillaris and separated from them by the blood-retinal barrier (BRB) [26]. The presence of the BRB prevents the leakage of macromolecules and other potentially harmful agents into the retina [27].

Pathogenesis of Retinopathy


Despite the considerable attention given to hypertension and its complications, the pathogenesis of hypertensive retinopathy, especially the onset of the lesions, is not yet fully understood. It is believed that the first changes that occur in response to elevated BP in the vessels of the retina are vasospasm and an increase in vasomotor tone, which manifests as generalized vessel narrowing [6]. This is a consequence of the local regulation of blood flow and an attempt to control the volume of blood in the vascular bed by myogenic and metabolic mechanisms [28]. Since the ARIC (Atherosclerosis Risk in Communities) study, the arteriovenous ratio (AVR) is the most widely used method for assessing generalized retinal vasoconstriction [29]. It is based on the diameters of the central retinal artery equivalent (CRAE) and the central retinal venular equivalent (CRVE), also known as the central retinal vein equivalent [30]. A study of 223 subjects, of whom 86 were normotensive and 137 had early hypertension (up to 1 year since first appearing), showed that people with hypertension had lower CRAE and AVR, while no significant difference in CRVE was observed. Furthermore, patients with hypertension and retinopathy showed more significant arterial stiffness indices, expressed by the pulse wave velocity (PWV) and aortic augmentation index (AIx) [31]. Also, a lower AVR predicts an increase in the 3-year risk of CHD events in females [32]. Another study proved that a decrease in CRAE and an increase in CRVE correlates with higher mean arterial blood pressure (MABP) [33]. This indicates a reduction in the vascular lumen in hypertension. Inconsistent data about whether the diameter of the veins in hypertension increases or does not change might suggest that venular widening is associated with retinal ischemia and hypoperfusion, which appear later in hypertensive retinopathy.


Continuously increasing blood pressure leads to arteriosclerosis. This results in an increase in blood flow resistance and a decrease in perfusion and, consequently, to retinal ischemia [34]. In addition, arteriosclerotic lesions cause several modifications in vessel architecture, such as intimal thickening, media-wall hyperplasia, and hyaline degeneration [34]. In fundoscopy, these changes manifest as a focal and diffuse narrowing of the arterial wall (resembling silver or copper wiring), accompanied by arteriovenous nicking, which is the result of increased pressure imposed on the venules by altered arterioles (Figure 1). Nicking is associated with both current and past BP, suggesting that it is a persistent and long-term marker of hypertension [18]. Observations carried out by Cheung et al have shown that increased arteriolar and venular tortuosity in the retina is also associated with chronic hypertension [35]. When hypertension is poorly controlled or reaches extremely high values, the damage progresses further. Over time this can lead to breakage of the BRB, the presence of hemorrhages, hard (lipid) exudates, and cotton wool spots, which are evidence of ischemia of the NFL [36]. Also, people with hypertension have been diagnosed with a lower amount of perifoveal arterioles and venules, and this may indicate gradual vascular occlusion and necrosis [37]. In advanced hypertension, an increase in intracranial pressure (ICP) can occur. When increased pressure of the cerebrospinal fluid is imposed on the optic nerve head and its vessels, it results in ischemia and edema of the optic disc (papilledema) [16,38,39].


The presented pathogenesis appears to reflect a cascade of changes that occur in the course of hypertensive retinopathy in an orderly way. However, recent research suggests that the whole process might be much more complex. Lesions visible at the fundus of the eye may occur in a different order; for example, the presence of hemorrhages is not always preceded by generalized vasoconstriction [40]. Also, arterial stenosis is observed among people without hypertension [41] as a result of changes in the retinal vascular caliber (arteriolar narrowing and venular widening). A large meta-analysis on a group of 10 229 subjects indicates that these changes in retinal vessel diameter are associated with a higher risk of hypertension, which develops for up to 10 years after the onset of the changes. This observation supports the theory that changes in retinal microcirculation can precede arterial hypertension [42,43]. A decrease in arteriolar caliber also correlates with older age and low birth weight, as well as with a higher hematocrit, higher white cell count, and higher platelet count [30,44]. A meta-analysis by Chew et al proved that there is a close link between a decrease in both retinal arteriolar diameter and CRA diameter and hypertension, and that each 10-mmHg increase in MABP is associated with a 3 μm decrease in mean retinal arteriolar diameter [45]. This reduction occurs because high BP causes a gradual entropic remodeling of the arterioles, resulting in a decrease in the outer and inner diameter of the vessel [46].


There are several mechanisms involved in the pathogenesis of hypertensive retinopathy. One of them is an elevated level of oxidative stress, expressed by an increase in the plasma markers gamma-glutamyltransferase and ferritin [47,48]. Other vital pathomechanisms are low-grade inflammation (increased high-sensitivity C-reactive protein, which is a marker of systemic low-grade inflammation, and is correlated with the prevalence and severity of hypertensive retinopathy) and increased platelet activation (the presence of hypertensive retinopathy correlated positively with urinary 11-dehydro-TXB2, a biochemical marker of platelet activation) [49–51]. Hypertension damages the vascular endothelium, which is located at the border between blood and the interstitial tissues. Its primary role is to control vasoregulation, hemostasis, and inflammation [52,53]. Nitric oxide (NO), which has an essential role in vasodilatation, is produced by the endothelial cells. The observation of the retinal flow after intravenous administration of NG-monomethyl-L-arginine (nitric oxide synthase inhibitor) in groups of normotensive and hypertensive patients showed significant changes. In the hypertensive group, the blood flow did not change, while in the group of normotensive patients the blood flow significantly decreased. This indicates a diminished role of NO-dependent vasodilatation in the regulation of blood flow among patients with hypertension and impaired endothelial function [54]. This was further confirmed in the hypertensive group by the elevated level of the von Willebrand factor, a substance which is stored in the endothelial cells, and by an increased concentration of angiotensin-converting enzyme (ACE, CD143), which is connected to their membranes [53].


The renin-angiotensin-aldosterone system (RAAS) plays a vital role in the regulation of systemic and local BP. Its primary function is to control the concentration of sodium and potassium ions in body fluids, which is crucial in regulating the volume of circulating blood. The role of RAAS has been widely studied in the course of diseases such as diabetic retinopathy (DR) and glaucoma [55]. However, there is no major study focusing on RAAS and its relationship with hypertensive retinopathy. This fact is of great importance because its excessive activity can damage the vascular bed through persistent vasoconstriction. However, a local increase in the concentration of RAAS components can cause proliferation and inflammation and stimulate neovascularization [56]. In human model studies, the presence of local RAAS in the eye was confirmed, and many known components of this system were identified in the eye, such as its main effector, angiotensin II (Ang II). Ang II, by acting on the angiotensin II receptor type 1 (AT1-R) causes vasoconstriction and stimulates cell proliferation and fibrosis [56,57]. The Mas-receptors (Mas-R), which are also located in the eye, when stimulated by the product of the breakdown of Ang II to angiotensin 1–7 (Ang 1–7), has the opposite effects to AT1-R (anti-inflammatory, inhibition of cell proliferation, antifibrosis, and vasodilatation) [58]. Ang 1–7 administration resulted in a decrease in IOP in the animal model. IOP was also lowered when patients with hypertension were treated with an angiotensin-converting enzyme inhibitor (Captopril) and an AT1-R antagonist (Losartan) [59,60]. This observation is important because high IOP can lead to retinal perfusion disorders due to increased pressure imposed on the retinal vessels. Another AT1-R blocker, candesartan cilexetil, showed a positive impact on the regulation of retinal blood flow by improving endothelial-dependent NO vasodilatation among patients with hypertension [54]. An important step to better understand the impact of RAAS in hypertensive retinopathy may be a recent research study on the Ang II-elevated double-transgenic rat model [61]. The study indicated that a high level of Ang II correlates with the degeneration of retinal ganglion cells and alterations in the outer layer of the BRB. The study also showed that retinal RAAS is regulated by systemic alterations of the systemic RAAS, which is mainly expressed by changes in renin production by the RPE [61]. Furthermore, an increase in the systemic Ang II level correlates with a decrease in the retinal RAAS activity, and β-adrenergic influence increases the retinal RAAS activity, but the role of this process is yet to be explored [62]. The main factors involved in the pathogenesis of hypertensive retinopathy are presented in Figure 2.


Neovascularization can have an essential role in the pathogenesis of hypertensive retinopathy. Angiogenesis is mostly controlled by a tight balance between pro-angiogenic and anti-angiogenic factors. Pathological mechanisms, such as ischemia, hypoxia, and inflammation, which cause endothelial damage, can promote neovascularization [63]. It should be emphasized that ischemia and hypoxia of the retina are important components of hypertensive retinopathy [64]. A review from 2012 highlights the potential role of the vascular endothelial growth factor (VEGF) family in the pathogenesis of hypertensive retinopathy. One of the best-known members of this family, VEGF-A, is crucial in neovascularization and is a major vascular permeability factor, whose increase correlates with essential hypertension [65]. VEGF is also an early marker of vascular endothelial damage [66]. Changes in its concentration can be significant in the early diagnosis of patients with microcirculation complications, such as hypertensive retinopathy. This is further confirmed by an increase in plasma VEGF levels in hypertensive patients with retinopathy [67]. VEGF can be released in response to hypoxia-mediated damage of the nerve fiber layer, and by activation of AT1-R [68]. A case report from 2016 first described a patient with proliferative retinopathy in the course of severe uncontrolled hypertension [69].

Diagnostics of Hypertensive Retinopathy


Recently, there has been significant progress in the area of visualizing the interior of the eye. Not only can large retinal vessels be observed, but it is also possible to go deeper to the level of the capillaries. The introduction of adaptive optics (AO) retinal imaging and optical coherence tomography (OCT) provided scientists with improved data on retinal vascular changes [75]. This is especially important for observing retinal microcirculation to predict cardiovascular risk [76]. Thanks to these new imaging techniques, the progression of the lesions can be closely monitored, as it makes it possible to perform vascular observation in vivo [77]. Spectral domain-OCT (SD-OCT) enabled faster scanning, denser sampling, and three-dimensional imaging [78]. A study using SD-OCT analysis on a group of 119 patients, 56 of whom had hypertension, showed that in the chronic stage (grade I and II of KWB) it is an accurate, reproducible, and convenient method for assessing CRA diameter, CRV diameter, and AVR [79]. In addition, SD-OCT showed a better correlation of these measurements with worsening visual acuity than the KWB classification due to the presence of subretinal fluid (SRF) in severely hypertensive patients (SBP >180 mmHg or DBP >110 mmHg). In their research, Ahn et al also proposed a new classification of hypertensive retinopathy based on OCT findings and consisting of 3 grades: mild-to-moderate, malignant without SRF, and malignant with SRF [80]. SD-OCT is also a useful tool for monitoring the decrease of retinal nerve fiber layer (RNFL) and the central macular thickness in grade IV hypertensive retinopathy [81]. The results of the Singapore Malay Eye Study highlight a link between a decrease in arteriolar and venular caliber and the thickening of RNFL, even after excluding patients with glaucoma [82]. Data from another study suggest that SD-OCT assessment should be added to standard hypertensive retinopathy evaluation in patients with systemic hypertension for the early diagnosis of HMOD [83].


OCTA provides a quick and non-invasive assessment of retinal microcirculation. Retinal and choroidal microvascular changes are evaluated based on parameters such as the vessel density (VD), the area of the foveal avascular zone (FAZ), and the radial peripapillary capillary (RPC) network [84]. The assessment of retinal capillaries has been effective in DR, and its use in hypertensive retinopathy can also be effective. It enables the detection of even subtle differences in the architecture of the capillaries, which might be the earliest markers of ischemia and hypoxia, before arteriolar and venular modifications take place [85]. Moreover, recent studies with OCTA analysis indicate that vessel density in SVP decreases in the group of hypertensive patients with inadequate BP control [86]. Also, the reduction in retinal and choroidal VD is strictly related to the coronary artery and branch stenosis, making OCTA an efficient and non-invasive method for measuring and detecting early-stage CHD, which can reduce the occurrence of MI [87]. It is also reasonable to perform SD-OCT and OCTA analysis simultaneously. Unlike SD-OCT, OCTA cannot measure retinal vascular diameter, but provides an evaluation of the hemodynamics and vascular density of retinal blood flow [64]. Takayama et al expressed the need to adopt a new classification system based on the usage of OCTA and the measurement of choroidal vasculature in the fovea proximity, which is also reduced in arterial hypertension [88]. They demonstrated that changes in the SVP, the FAZ area, the capillary density, and the inner retinal thickness occurred in the group of hypertensive patients without hypertensive retinopathy. As mentioned earlier, subtle modifications in the vasculature can develop before the onset of hypertension. This implies that increased OCTA follow-up frequency may be useful for the supervision of retinal vascular and thickness changes in the group of patients at risk of developing hypertension [89].


AO retinal imaging is another important tool in the precise visualization of retinal vasculature. With a resolution of less than 2 μm, it improved the quality of retinal images and helped in the assessment of cellular and subcellular details such as the condition of the endothelial cells and subtle fluid leakage [90]. The use of this technique enables direct measurement of the retinal vessel wall (VW) and the lumen diameter (LD). A semi-automated method used to measure vessel parameters had low intra-observer variability [91]. The wall-to-lumen ratio (WLR) is another effective vascular parameter that can be measured by coupling AO with scanning laser ophthalmoscopy (Figure 3) [92]. The increase in the WLR that occurs in hypertension is caused by a decrease in LD and the thickening of the arteriolar wall (Figure 4). This is used to detect subtle retinal microvascular modifications observed in the early remodeling process [93]. Its importance extends further, as an increase in the WLR correlates not only with age and with higher body mass index (BMI), but also with early-stage HMOD [94,95]. More extensive use of AO retinal imaging will be essential in the search for novel mechanisms of hypertension-related vascular alterations. It has already improved our understanding of the significance of capillary level changes in perfusion [90].

Therapeutic Approaches

Currently, the approach to the treatment of hypertensive retinopathy focuses mainly on the control of systemic BP within the limits of the norm, which is primarily achieved by oral pharmacotherapy. A decrease in BP obtained by the use of ACE-inhibitors can reduce the risk of progression of hypertensive retinopathy changes [96]. Also, such therapy results in an improvement of arteriolar architecture and rarefaction, and an increase in arteriolar density [97, 98]. In contrast to more severe retinopathy, an early manifestation is more likely to be reversible. For this reason, early detection of retinopathy lesions might prove helpful not only in the effective prevention of its further development but also in searching for new therapeutical opportunities [99]. The major obstacle in therapy based mainly on oral drug administration is poor compliance. A 2017 meta-analysis on a group of 12 603 hypertensive patients found non-adherence to pharmacotherapy in 45.1% of patients [100].

The latest reports also suggest that severe lesions associated with malignant hypertensive retinopathy can regress or even completely disappear. Strachan and McKnight described the case of a 34-year-old woman diagnosed with hypertension and stage IV hypertensive retinopathy on the KWB scale. Changes visible at the fundus of the eye retreated after 10 months of irbesartan (AT1-R antagonist), atenolol (β1-adrenergic antagonist), and amlodipine (a calcium channel blocker) therapy [101]. Another case report focused on a 23-year-old patient with deterioration in vision and malignant hypertensive retinopathy, which appeared 1 month after ceasing antihypertensive drugs. Six weeks after returning to pharmacotherapy, the signs of malignant hypertensive retinopathy disappeared, and visual acuity improved [102]. In addition, the presence of pheochromocytoma, a tumor that is characterized by frequent spikes in BP, can lead to rapid development of malignant hypertensive retinopathy. Treatment based on adrenalectomy and normalization of BP values was successful, and improvement of optic disc edema and hard and soft exudates was observed [103].

Unfortunately, there is a lack of research focusing primarily on the therapy of retinal lesions appearing in the course of hypertension. Most information on new directions of treatment come from case reports and studies with small sample sizes. One promising approach was based on the correlation between systemic hypertension and increased IOP. There were attempts to use topical administration of IOP-lowering drugs in systemic hypertension to improve blood flow and arteriolar blood saturation might. However, the application of timolol (β-adrenergic receptor antagonist) and dorzolamide (carbonic anhydrase inhibitor) had no effect or a minimal effect on retinal blood flow [104]. Interestingly, a recent report suggests that a diet rich in L-methylfolate and vitamin D might be beneficial for patients with hypertensive retinopathy. However, this approach needs to be confirmed in a larger group of patients [105].

Targeting neovascularization, which may play an essential role in the pathophysiology of hypertensive retinopathy, appears to be encouraging. Bevacizumab, an anti-VEGF antibody, is widely used in ophthalmology for the treatment of diseases associated with increased vascular permeability, such as exudative age-related macular degeneration (AMD) and DR [106]. Vascular leakage also appears in the course of malignant hypertensive retinopathy. When hypertensive retinopathy enters its exudative stage, BRB damage and increased vascular permeability occurs [36]. Intraocular injections of anti-VEGF antibody were used successfully in 2 patients with hypertension and malignant hypertensive retinopathy with the presence of macular and optic disc edema. One month after the injection, visual acuity improved, and the lesions characteristic of the exudative stage disappeared [107]. This is not the only report of the possible effectiveness of anti-VEGF antibody treatment in malignant retinopathy. Three other cases, 2 with the use of Bevacizumab and 1 with the use of Ranibizumab, which is also an anti-VEGF antibody, confirmed their efficacy [108–111]. The decision to apply a Ranibizumab injection was based on the lack of improvement in the retinal image in the course of malignant hypertensive retinopathy, despite extensive BP control. Therefore, targeting VEGF and neovascularization as a potential pathomechanism of malignant hypertensive retinopathy appears to be reasonable.

Predictive Value of Hypertensive Retinopathy


Changes in the retina that indicate a significant progression of retinopathy have been proven to be strongly associated with the occurrence of cardiovascular diseases. Advanced lesions can predict congestive heart failure and cardiovascular mortality, independent of BP and other risk factors [112]. Wang et al analyzed the results of 2 extensive cohort studies, the Beaver Dam Eye Study and the Blue Mountains Eye Study, which both assessed the diameter of the retinal vessels. These studies made it possible to establish a link between retinal vascular diameter and risk of CHD and stroke in middle-aged persons [113]. Another meta-analysis of over 21 000 patients indicates that both narrower retinal arterioles and wider retinal venules are correlated with a higher risk of CHD in women, but not in men. The above findings might support the thesis that coronary microvascular dysfunction plays an important role in the pathogenesis of CHD [114,115].

Hypertension, especially when insufficiently controlled or untreated, leads to the development of left ventricular hypertrophy (LVH). Previous studies have shown a close association between advanced hypertensive retinopathy and LVH, and that hypertensive retinopathy doubles the risk of LVH [116]. The results of recent research suggest that retinal arteriole narrowing may be as accurate as BP measurement in predicting LVH [117,118]. The coincidence of changes in retinal vessel diameter and HMOD, expressed as LVH and ventricular remodeling, has also been studied. Based on the images of digital retinography performed in hypertensive patients, AVR was shown to be correlated with the presence of HMOD in the form of LVH [119].


The evaluation of retinal arterioles is a model for assessing cerebral microcirculation, thanks to their great proximity, anatomical resemblance, and mutual vascularity (internal carotid artery supplies both the anterior brain and the retina) [120]. Hypertensive retinopathy has been proven to predict the long-term risk of stroke, even among patients with good hypertension control [12]. This suggests that the precise control of retinal microvasculature is of additional value in predicting vascular risk [121]. There is also evidence based on cohort studies that retinal microvascular changes are associated with dementia, cognitive impairment, and brain imaging abnormalities. The correlations are strongest for more severe retinal microvascular abnormalities [122].


The development of chronic kidney disease (CKD) can occur due to severe hypertension. A study on a group of 224 non-diabetic CKD patients with hypertension showed that over 70% had hypertensive retinopathy. Furthermore, retinopathy advancement was independently associated with CKD severity, which was later confirmed in other studies [123, 124]. Recent research indicates that there is a lower density in both SVP and DCP among patients with simultaneous CKD and hypertension [125]. It has also been reported that the low retinal vascular density found in OCTA is associated with acute kidney injury (AKI) and can predict its onset [126].

On the contrary, Vaes et al showed that there is a lack of association between retinal vessel diameter and lung function parameters among patients diagnosed with chronic obstructive pulmonary disease (COPD) [127].

New Directions of Research


Currently, there is an increasing number of studies in the field of hypertensive retinopathy. The majority of them are focused on better understanding the pathogenesis of this disease. One study indicated that endothelins, a group of vasoconstrictive agents produced by the endothelial cells, can cause BRB damage. It is mainly caused by the activation of endothelin receptors A and B (ETRA and ETRB) by endothelin 1 (ET-1). Stimulation of these receptors promotes vascular leakage and VEGF stimulation and is upregulated in the animal model of hypertension and diabetes. In addition, the antagonists of these receptors have been shown to reduce vascular damage and neovascularization, and have demonstrated a protective effect on the BRB. Also, the plasma ET-1 level is elevated in hypertensive retinopathy [128,129]. It is crucial to further explore the role of neovascularization in hypertensive retinopathy, as this might help achieve an additional therapeutical effect. Targeting the agents promoting neovascularization, such as platelet-derived growth factor (PDGF), pigment epithelium-derived factor (PEDF), hepatocyte growth factor (HGF), angiopoietins, and fibroblast growing factor (FGF), may be promising [130]. Research on the rat model of hypertensive complication of pregnancy, preeclampsia, confirmed the relationship between high BP, RAAS, and an increased level of pro-angiogenic factors, such as VEGF and PEDF. In preeclampsia, there is a massive endothelial dysfunction, which also causes slight retinal vessel narrowing [131]. Proteomic analysis of the vitreous humor might help to define the involvement of these factors in the pathogenesis of hypertensive retinopathy, thanks to its proximity to the damaged retina. One of the difficulties of this method might be the small sample size [132].


Genetic testing can also provide new data. There have been attempts to locate the genes responsible for the diameter of the retinal vessels. So far, 8 single-nucleotide polymorphisms (SNPs) for CRVE and 2 for CRAE have been identified. Further research on their involvement in microvascular diseases might explain a predisposition to microcirculation disorders [133]. In addition, polymorphisms of ALK-1 and endoglin have been shown to be risk factors of cardiovascular events. Both ALK-1 and endoglin are transforming growth factor β1 (TGF-β1) receptors, which have a place in the regulation of BP and vascular homeostasis. In addition, it has been proven that TGF-β1 is involved in the thinning of the basal lamina of capillaries, a scaffolding for epithelium cells [134].


Serum uric acid (SUA) concentration is an independent risk factor for hypertension. As a large study on the Chinese population showed, it is also associated with hypertensive retinopathy. Elevated levels of SUA might lead to endothelial cell damage. In addition, the additional occurrence of high BP might have a negative cumulative effect on microcirculation and can be a mediator of vascular damage. It is possible that by reducing the SUA level, the risk of hypertensive retinopathy might be diminished [135]. Another substance, marinobufagenin, which is a biomarker of salt sensitivity that increases with salt intake, was found to be associated with reduced retinal microvascular artery dilatation in young normotensive adults. In addition, increased levels of marinobufagenin have been shown to promote endothelial damage and prevent BP reduction during the night, which is a physiological process [136].


There is significant emphasis on inflammation and its relationship with retinal microcirculation damage. The role of LMP10, a catalytic subunit of proteasome induced by interferon-γ with trypsin-like activity, has been emphasized. Ang II can cause upregulation of this subunit, and research on the mouse model and humans has shown its increased level and activity in the retina in hypertension. Moreover, knockout of LMP10 has attenuated the increase in retinal vascular permeability, remodeling, and inflammation. The inhibition of this subunit might be a potential therapeutic agent [137]. Another subunit of proteasome, β5i, has been shown to have a significant role in developing hypertensive retinopathy in the mouse model of hypertension. The β5i subunit decreases the stability of AT1R associated protein (ATRAP), which generally inhibits AT1R mediated retinopathy. Deletion of β5i alleviated the retinal thickness induced by Ang II, inflammation, oxidative stress, and remodeling. Overexpression tends to aggravate these effects [138]. A different study on the mouse model with hypertension has shown that G-protein coupled receptor 174 (GPR 174) plays a vital role in the regulation of the immune and inflammatory response. Knockout of the gene for this protein caused a decrease in vascular permeability and had a protective effect on the retina [139]. A recent study proposed glycoprotein acetyls (GlycA) as a new marker of chronic and cumulative inflammation. High GlycA levels were reported to be correlated with a wider venular caliber and narrower arteriolar caliber [140]. The association between GlycA and hypertensive retinopathy is yet to be examined.


Establishing a suitable experimental animal model for hypertensive retinopathy might contribute to significant progress in this field. Recently, a hypertensive BPH/2J mouse model was introduced that might be favorable for future diagnostics and research on retinal damage. It presents a similar hypertensive surge as that observed in humans [141]. A recent study on the well-known animal model of hypertension, spontaneously hypertensive rat (SHR), has shown that inhibition of an isoform of reactive oxygen-producing enzymes, NADPH oxidase (Nox), might prevent hypertension-related loss of vision. Inhibition of Nox 1 and Nox 4 had a protective effect on the BRB by the reduction of inflammation and the oxidative stress level. Inhibition of Nox 5 reduced retinal neovascularization and vascular permeability [142].


This review has shown that hypertensive retinopathy has a complex pathogenesis. Several damage processes might be involved with the probable essential role of neovascularization. Damage to the microvasculature may not be apparent on routine retinal examination. However, the combined use AO with OCT has begun to show how and when neovascularization may be a therapeutic target in hypertensive retinopathy.


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Medical Science Monitor eISSN: 1643-3750
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