Glaucoma is a potentially a blinding condition, a disease which exhibits a characteristic optic neuropathy which may result in progressive visual field loss. (Kanski, 2006). Glaucoma was considered a neurological disease, as the association in raising intraocular pressure (IOP) occurred over several centuries but was boosted by apparatus improvements in tonometer between 1880 and 1910. (Paul N.Schacknow and John R.Samples, 2010). Development of ocular measurement apparatus and findings can create a new concept that may change the terminology of glaucoma. Yet, IOP is known to be the major risk factor among others which is proven in so many cases around the world. (Quigley et. al, 2006).
Glaucoma has been highlighted to be the second largest cause of blindness in the world and it getting increase yearly. It has been expected to increase by 79.6 million by year 2020 with 74% of these will be Open Angle Glaucoma (OAG). (Quigley et. al, 2006). The status as the second largest cause of blinding glaucoma were also agreed by Leske M.C., 2007 but there are various gap of etiology that need further clarification to allow better comparability across studies. Identifying through the risk factors helps glaucoma condition to be clearly understood the way it effect the patients and other related complications. The goal of identifying the risk factors for glaucoma is to recognize the possibility of patient with greater risk to have a symptomatic visual loss that effect their quality of life. (Keith E. et. al, 2009).
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General risk factor for glaucoma had been long discussed which include the age, race, family history, ocular risk factors (IOP, Optic nerve head features), myopia, systemic risk factors (diabetes mellitus, young age, inadequate IOP control, high rate of progression despite treatment). (R. Rand Allingham et. al, 2005). Elevation in intraocular pressure (IOP) has long been considered to be the primary cause of glaucoma. High in IOP usually defined as greater than 21mm mercury (Hg). However, even people with normal pressures can develop glaucoma too. Many research shows that taking eye drops can help to lower the IOP elevation to diminish the risk of glaucoma. Although having 21mmHG of IOP, this does not mean that we have glaucoma but considered as a risk factor. Upward of six million people in United States have elevated IO without demonstrable perimetric visual field damage. (Kreuger D.E. et. al, 1980; Armaly M.F. et. al, 1980; Quigley H.A. et. al, 1994).
In black people, open angle glaucoma is the leading cause of blindness and is 6~8 times more common than in Caucasians. It is also been notified that the risk is high for people who is over 40 years of age. As for Asian and Eskimos, more likely to develop closed-angle glaucoma than other races.
A recent large clinical trial discovered that patients with thinner corneas (the clear structure at the front of the eye) are at an increased risk of developing glaucoma. They also found that African-Americans have thinner corneas than Caucasians.
Patient with corneal thickness less than 555microns have three fold greater risk of developing glaucoma as compared with those who's cornea are more than 588microns thick. Some specialist believe that there is a common collagen abnormality found in both cornea and lamina cribosa that predisposes patient to glaucoma. Although corneal thickness is part glaucoma risk factor, this has not yet translated to clinical applicability as many question about corneal thickness remain unanswered.
Age is another risk of getting glaucoma after age of 50. Some other finding suggest that at age of 40 the risk of getting glaucoma is true for black people. However, glaucoma can occur in anyone at any age which include congenital & juvenile glaucoma. Since majority glaucoma recorded comes from older citizen, priority of the risk glaucoma were classified to be 50 years of age.
Hereditary were also considered as a risk factor for glaucoma disease. In case of congenital glaucoma that appears in the first months of life, eventually at birth or in utero. Congenital glaucoma is characterized by minor malformations of the irido-corneal angle of the anterior chamber of the eye. Other observation finding include tearing, photophobia and enlargement of the globe appearing in the first month of life. Heredity of congenital glaucoma is autosomal recessive which involve CYP1B1, GLC3A and GLC3B. (http://www.orpha.net/data/patho/Pro/en/GlaucomaHereditary-FRenPro3563.pdf). Juvenile glaucoma is considered as a primary open angle glaucoma which appearing during first two decades of life. Primary open-angle glaucoma has high IOP elevation (> 21mmHG), excavation of the optic nerve head & lost of visual field. POAG is the most prevalence type of glaucoma, affecting 1 in 100 population of 40 years of age. Treatment involve medical and often surgical. Heredity is autosomal dominant, and there are two genes that have been identified, MYOC (myocilin genes) on chromosome 1q21-q31 and optineurin gene in the GLC-1E interval on chromosome 10p. (Kanski, 2007, Wiggs J.L, 1994). Myocilin is still poorly understood in POAG and a study of group of unrelated POAG patients found myocilin mutations in at least 4% of the adult patients. The equivalent of hereditary process to have genetic myocilin mutation is up to 33% if any of family member at age 35 who develop glaucoma to be pass on to their heir.
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References of chapter 1.
Jack J Kanski, (2007). Clinical Opthalmology A Systemic Approach. 6th Edition, Butterworth Heinemann Elsevier.
Paul N.S. & John R.S., (2010). The Glaucoma Book: A Practical, Evidence-Based Approach to Patient Care. Springer.
Quigley, H.A., Broman A.T., (2006). The number of people with glaucoma in 2010 and 2020, Vol 90, Issue 3, 262-267.
Keith E., Simon K.L., John W., Patricia B., Jan H, (2009). The quality of life impact of peripheral versus central vision loss with a focus on glaucoma versus age-related macular degeneration, Vol 3, 433-445.
Wiggs J.L., Haines J.L., Paglinauan C., Fine A., Sporn C., Lou D., (1994). Genetic linkage of autosomal dominant juvenile glaucoma to 1q21-q31 in three affected pedigrees, Vol 21(2), 299-303.
Kreuger D.E., Milton R.C., Maunder L.R., (1980). The Framingham eye study: introduction to the monograph, Vol 24(6), 614-20.
Armaly M.F., Kreuger D.E., Maunder L., Becker B., Hetherington J.Jr., Kolker A.E., Levene R.Z., Maumenee A.E., Pollack I.P., Shaffer R.N., (1980). Biostatistical analysis of the collaborative glaucoma study. I. Summary report of the risk factors for glaucomatous visual-field defects, Vol 98(12), 2163-71.
Quigley H.A., Enger C., Katz J., Sommer A., Scott R., Gilbert D., (1994). Risk factors for the development of the glaucomatous visual field loss in ocular hypertension, Vol 112(5), 644-9.
R. Rand Allingham, M. Bruce Shields, Sharon Freedman, (2005). Shields' textbook of glaucoma. 5th Edition, Lippincott Williams& Wilkins, Philadelphia USA.
Leske M.C., (2007). Open-angle glaucoma - an epidemiologic overview, Vol. 14(4), 166-72.
2.1 Evidence of Ocular Blood Flow Changes
Theoretically, there are 3 components contributing to ocular blood flow reduction in glaucoma patients ; (1) increased local resistance to flow, (2) decreased ocular perfusion pressure (OPP), and (3) increased blood viscosity. (Shaarawy et. Al, 2009). All these component shows that ocular blood flow is important for us to understand the pathology & process of defect in glaucomatous eye.
The result indicate that nimodipine increases optic nerve head (ONH) and choroidal blood flow in normal tension glaucoma (NTG) patients and inproves color contrast sensitivity (CCS). The latter effect does not, however, seems to be direct consequence of the blood flow improvement. (Lukschet et. al, 2004). Dorzolamide/timolol fixed combination increased blood flow significantly at the neuroretinal rim showing a combination of hypotensive and heamodynamic effects. (Rolle et. al, 2008). These findings shows drug effect could induce changes on ocular blood flow and it proves that blood flow measurement is a worthy findings towards glaucomatous progression in the eye.
The neuroretinal rim is the tissue between the outer edge of the cup and the disc margin. The normal healthy rim has an orange or pink colour and shows a characteristics configuration. The inferior rim is the broadest followed by the superior, nasal, and temporal, ISNT. (Kanski, 2007). Eyes with and without cilioretinal did not differ significantly in the areas of neuroretinal rim and alpha (Î±) and beta (Î²) zones of parapapillary atrophy, when measured in the whole optic disc and in the 4 sectors separately; in ratios of the temporal horizontal area to total area of rim and parapapillary atrophy; and in the ratio of temporal rim area to nasal rim area, neither in an interindividual comparison nor in an intraindividual intereye comparison. In contrast to the position of the central retinal vessel trunk, presence and position of cilioretinal arteries do not markedly influence the pattern of neuroretinal rim loss and progression of parapapillary atrophy in glaucoma. (Wido et. al, 2003). In some other findings, an important morphologic predictive factors for progression of the glaucomatous appearance of the optic nerve head in white persons are small size of neuroretinal rim and large area of Î² zone of parapapillary atrophy. Progression of glaucomatous optic nerve head changes is independent of size and shape of the optic disc, size of Î± zone of parapapillary atrophy, retinal vessel diameter, and optic cup depth. (Jonas et. al, 2002). Both research above suggest that, there were no direct relation between the blood flow and neuroretinal rim changes in glaucomatous eye.
Findings in early 2000, glaucoma patients exhibit reduced ocular blood flow at the neuroretinal rim, which seems to affect high velocity flow more profoundly than low velocity flow. (Hosking et. al, 2001). The glaucoma subjects had significantly lower the retinal haemodynamics than the control subjects. There were no significant differences in HRF parameters between the NTG and POAG subjects. The discs had been identified as having abnormal segments had lower HRF values than those with a corresponding normal segment. Logan et. al, 2004 study show the relation between structural damage of the optic nerve head and the level of retinal blood flow and this may indicate an early marker of the pathological process. On the other research findings, specific location is identified that inferior sector of retinal nerve fibre layer and the optic nerve head may have lower blood flow per unit nerve tissue volume compared to the superior sector. This results suggest that the inferior sector is more vulnerable to elevated intraocular pressure (IOP) and ischaemic insults in glaucomatous optic neuropathy. (A Harris et. al, 2003). Hafez et. al, 2003 stated that mean neuroretinal rim blood flow was significantly higher in OHT patients with C/D ratios less than 0.4 when compared to OHT patients with larger C/D ratios. This suggests that reduce neuroretinal rim blood flow in higher risk ocular hypertension may be an early event in the development of glaucomatous optic neuropathy, appearing prior to the manifestation of visual field defects. Changes in neuroretinal rim & changes in blood flow works along as an early sign to manifest visual field defect.
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Association between blood flow measurement in cup & pulsation amplitude in cup, and association between mean defect from visual field testing and ocular hemodynamic parameter were also significant. Reduced optic disc perfusion in patients with open-angle glaucoma is evidenced from two independent methods in the present study. Moreover, the data indicate that reduced ocular blood flow in these patients is linked to visual field changes. It remains to be established whether compromised optic disc and choroidal blood flow contributes to optic disc damage in glaucomatous eye or is a secondary functional phenomenon. (Findl O. et. al, 2000). Ocular blood flow alteration in glaucoma patient seems, at least partly, to be related to a systemic vascular dysregulation. (Emre et. al, 2004). There is another follow up findings, states that, for subjects with asymmetric glaucoma damage between eyes, flow and velocity were significantly lower in the eyes with worse glaucoma damage. When comparing optic disc displaying within-eye asymmetry, the hemidisc with greater damage showed significantly lower blood velocity than the hemidisc with less damage, but however, no difference in blood flow or volume was detected. This provide evidence that impaired optic nerve circulation is associated with the extent of glaucomatous pathology. (Andrew et. al, 2005).
Inferior rim blood flow is less than superior rim blood flow in patients with superior hemifield defect, and superior rim blood flow is reduced compared to the inferior in patients with inferior hemifield defect. The blood flow in the neuroretinal rim was found to correspond to the regional visual field defect in eyes with NTG. Reduction in flow were associated with reduction in function. (Sato et. al, 2006).
2.2 Drug effect on optic disk blood flow with glaucomatous eye.
Some evidence of blood flow deficit in glaucoma derived from flourescein angiography since flourescein is a safe consistent drug to be use for staining and should be considered in high-risk patients. (Kwan A.S. et. al, 2006). Previous findings conducted by Harris A. et. al on NTG patients found that dorzolamide also accelerated retinal arteriovenous passage time (AVP) of flourescein dye, at constant retinal arterial and venous diameter, but failed to change flow velocities in any retrobulbar vessel. (Harris A. et al, 1999). Similar findings were found on healthy volunteers by using brinzolamide which reduction IOP level but showed no significant change in retrobulbar haemodynamics, but shortening of AVP. Since in glaucoma AVP is prolonged indicating vascular dysfunction this effect might be beneficial in glaucoma therapy. (Kaup M. et. al, 2004). Dorzolamide is a carbonic anhydrase inhibitor, an anti-glaucoma agent and topically applied in the form of eye drop was treated as placebo drug. Following study with dorzolamide found that there is no measureable vascular effects from topical dorzolamide treatment in previously untreated glaucoma eyes. (Bergstrand I.C. et. al, 2002). According to Ali S.H. et. al, reduction of IOP in OAG after therapeutic IOP reduction had a statistically significant improvement of blood flow in neuroretinal rim of the ONH, where as OHT patients does not demonstrate any changes. (Ali S.H. et. al, 2003).
Another topical drug can be use to reduce IOP elevation is latanoprost. A study has been conducted to evaluate the effect of a single instillation of latanoprost on human ONH and retinal circulation within certain time. Yasuhiro T. et. al found that tissue blood velocity in the ONH increased at least temporarily following a single instillation of topical latanoprost even the mechanism of the increases remain unclear. This may indicate that the effect of latanoprost on ONH tissue circulation in human may have clinical implication. (Yasuhiro et. al, 2004). The usage of topical nipradilol caused a transient, but significant increase in the ipsilateral ONH blood velocity after twice instillation in a week which indicate that the increase in ONH blood velocity in human was not a secondary effect accompanied by a decrease in IOP in the ipsilateral eye. (Ken M. et. al, 2002). This may be nipradilol attribute on vasodilative action. (Okamura T. et. al, 1996). It had been reported that topical nipradilol increases the ONH blood velocity in rabbits and suggest is partly attributable to local penetration of the drug. (Kanno K., 1998). Similar scenario also had been reported with topical betaxolol. (Araie M. et. al, 1997). Nipradilol also has been use in dogs, whereby reduction of IOP by nipradilol was similar to that by an existing Î²-adrenergic antagonist, timolol maleate, but nipradilol was associated with fewer systemic side effects in dogs. Nipradilol lowered IOP to an equivalent degree to timolol maleate but its hard enough to evaluate blood flow relationship between human and animal ocular haemodynamics. (Maehara S., 2004).
Findings through topical unoprostone also effect the tissue blood velocity in the ONH, the author recorded and increase temporarily following instillation of unoprostone twice daily for 7 days. The increment implication is unclear but the effect of topical unoprostone on human ONH circulation deserve further consideration. (Yasuhiro T. et. al, 2004).
Ocular blood flow appears to be related to any disease that involve blood circulation. As for epilepsy patients exhibit reduced neuroretinal capillary blood flow, volume, and velocity compared with normal subjects. A reduction in ocular perfusion may have implication for visual function in people with epilepsy. (Emma J.R.H., 2002).
Study also shows that the usage of dormolamide increase the blood flow in temporal neuroretinal rim and the cup of the optic nerve head, and fundus pulsation amplitude. (Fuchsjager-Mayrl G. Et. al, 2005). Recent study done by Andrzej S. et.al, additive effect of dorzolamide hydrochloride (Trusoft) and a morning dose of bimatoprost (Lumigan) on IOP and retrobulbar blood flow in patients with POAG reduces IOP significantly with these combined treatment whereby the vascular resistance in ophthalmic artery decreases. (Andrzej S. et. al, 2010). Vascular retinal artery in untreated or progressive POAG after treated with topical 2% of dorzolamide for 2 weeks show increase in diameter, velocity, and flow in response to normoxic hypercapnia. Similar trends were noted for ONH vascular reactivty too. (Subha T.V. et. al, 2010). Most of the study shows that the ocular blood flow is a good indicator for pathogenesis of glaucoma and it proves that blood flow measurement is a worthy findings to be exposed.
References of chapter 2
Kwan A.S., Barry C., McAllister I.L., Constable I., (2006). Fluorescein angiography and adverse drug reactions revisited: the Lions Eye experience, Vol. 34(1), 33-8.
Harris A., Arend O., Kagemann L., Garret M., Chung H.S., Martin B., (1999). Dorzolamide, visual function and ocular hemodynamics in normal-tension glaucoma, Vol. 15(3), 189-97.
Bergstrand I.C., Heijl A., Harris A., (2002). Dorzolamide and ocular blood flow in previously untreated glaucoma patients: a controlled double-masked study, Vol. 80(2), 176-82.
Ali S.H., Regina L.G.B., Michele R., Mark R.L., (2003). Changes in optic nerve head blood flow after therapeutic intraocular pressure reduction in glaucoma patients and ocular hypertensives, Vol. 110, Issue 1, 201-210.
Kaup M., Plange N., Niegel M., Remky A., Arend O., (2004). Effects of brinzolamide on ocular haemodynamics in healthy volunteers, Vol. 88(2), 257-62.
Emma J.R.H., Sarah L.H., Tim B., (2002). Epilepsy Patients Treated with Antiepileptic Drug Therapy Exhibit Compromised Ocular Perfusion Characteristics, Vol. 43, Issue 11, 1346-1350.
Yasuhiro T., Miyuki N., Makoto A., Ken T., Sawako S., Atsuo T., (2004). Topical Latanoprost and Optic Nerve Head and Retinal Circulation in Humans, Vol. 17, Issue 5, 403-411.
Okamura T., Kitamura Y., Uchiyama M., (1996). Canine retinal arterial and arteriolar dilatation induced by nipradilol, a possible glaucoma therapeutic, Vol. 53, 302-310.
Kanno K., Araie M., Tomita K., Sawanobori K., (1998). Effects of topical nipradilol, a ß-blocking agent with -blocking and nitroglycerin-like activities, on aqueous humor dynamics and fundus circulation, Vol. 39,736-743.
Araie M., Muta K. (1997). Effect of long-term topical betaxolol on tissue circulation in the iris and optic nerve head, Vol. 64,167-172.
Ken M., Takashi K., Naohiro S., Mikio F., Miyuki N., Atsuo T., Yasuhiro T., Makoto A., (2002). Topical Nipradilol: Effect on Optic Nerve Head Circulation in Humans and Periocular Distribution in Monkeys, Vol. 43, 3243-3250.
Maehara S., Ono K., Ito N., Tsuzuki K., Seno T., Yokoyama T., Yamashita K., Izumisawa Y., Kotani T., (2004). Effects of topical nipradilol and timolol maleate on intraocular pressure, facility of outflow, arterial blood pressure and pulse rate in dogs, Vol 7(3), 147-150.
Tamaki Y., Araie M., Tomita K., Nagahara M., Sandoh S., Tomidokoro A., (2004). Effect of Topical Unoprostone on Circulation of Human Optic Nerve Head and Retina, Vol. 17, Issue 6, 517-527.
Fuchsjager-Maryl G., Wally B., Rainer G., Buehl W, Aggermann T., Kolodjaschna J., Weigert G., Polska E., Eichler H-G., Vass C., Schmetterer L., (2005). Effect of dorzolamide and timolol on ocular blood flow in patients with primary open angle glaucoma and ocular hypertension, Vol 89, 1293-1297.
Subha T.V., Chris H., Rony R., Yvonne M.B., Samuel N.M., Joseph A.F., Graham E.T, John G.F., (2010). Retinal Artery Vascular Reactivity in Untreated and Progressive Primary Open-Angle Glaucoma, Vol 51, 2043-2050.
2.3 Autoregulation of the blood flow of the optic nerve head
Autoregulation is the ability of a vascular bed to maintain blood flow despite changes in perfusion pressure. In other words, autoregulation may also refer to the intrinsic ability of tissue to maintain relatively constant blood flow in the face changes in perfusion pressure or its ability to modify blood flow response to varying metabolic demand. Optic nerve head (ONH) partly shares blood flow physiologic of the brain and act as a continuation of the central nervous system. (Flammer J. and Orgul S., 1998). Central retinal artery (CRA) is the only source of the blood supply and feeds the retinal arteries. These distal vessel nourish the retinal ganglion cells and the confluence of unmyelinated nerve fibres anterior to the lamina cribosa. (Onda E. Et. Al, 1995). Previous literature have conclusively shown that glaucoma is a disease that cause the death of the retinal ganglion cells and erosion of the optic nerve head. Regulation of the blood flow is important during posture change to maintain proper circulation status in many organs. In a condition of upright posture, the gravity pulls the blood away from organs above the heart and towards organs below the heart. Appropriate blood flow is ensured by constricting the vessel to block hyperaemia and oedema when changing from supine to upright posture while the vessels above the heart dilate to offset falling perfusion. Evans D.W. et. al (1999), proved that glaucoma patients demonstrate faulty autoregulation of ocular blood flow during posture change. Another extensive research, the anatomy of the microvascular and the blood flow regulation of the ONH remains difficult to ascertain according to Harris A. et.al (2003). Recent study to assess the autoregulation retinal blood flow in healthy young subject, along with the systemic blood pressure and IOP suggest no significant change in retinal blood flow was found. This prove that a normal subject has the ability to compensate the increase of blood pressure and maintain a stable retinal blood flow after exercise. (Lester M. Et. al, 2007).
Cerebral circulation was proved to be dependent on local blood gas perturbations. (Haggendal et. al, 1969). These finding may also applied at autoregulation of ONH as the blood flow decreases, whereby the local metabolic vascular response is primarily oxygen-dependent. (Kontos et. al, 1978). According to Flammer et. al (1998), hypocapnia and hyperoxia mediate arteriolar constriction and a subsequent decrease in ONH blood flow, while hypercapnia and hypoxia does not show any significant. (Flammer and Orgul 1998). Research on inhalation of different mixture of oxygen and carbon dioxside may effect retinal blood flow. Retinal blood velocity, retinal vessel diameter and retinal blood flow were found to be decreased during all breathing periods as the mixture of gases had little effect on systemic haemodynamics. (Luksch A. et. al, 2002). Breathing with totally oxygenated environment can cause increase in oxygen saturated level (SaO2) and a decrease in end-tidal carbon dioxide (EtCO2). The test was done with 20 young adult in pure oxygenated room to understand the changes in retinal vessel diameter during physiological stress or pathologic conditions. Although the study were based on individual fundus photograph, the main objective was to detail the time course and amplitude changes in the diameter of arteries and veins across all retinal quadrants, during and after hypertoxic vascular stress. The findings shows that during systemic hypertoxic stress, the retinal vessels change in calibre uniformly across retinal quadrants in healthy young adults. (Jean-Louis et. al, 2005). Research of The Singapore Malay Eye Study done by Koh et. al (2010), cross-sectional study was conducted in Malay persons anged 40-80 years residing in Singapore, by using confocal scanning laser ophthalmoscope, optic disc measurements including disc area, rim area, and rim-to-disc area (RDA) ratio were taken. A significant findings of global RDA ratio suggest retinal venular tortuosity demonstrated a stronger association with RDA ratio compared to the arteriols. Thinning of neuroretinal rim were significantly associated with straight retinal vessel. Geometric retinal vascular changes noticeable in early glaucomatous optic neuropathy, this findings may provide an additional fact about blood vessel architecture and its role in physiology. (Koh V. Et. al, 2010). Additionally, concentration of K+, H+, adenosine, and intercellular osmolarity are known to effect local vascular tone. (Orgul et. al, 1995a).
The mechanism of autoregulation depends on 2 type of stimuli, metabolic and myogenic whereby can induce an autoregulatory responce from local vasculature. (Johnson P.C., 1986). Metabolic stimuli can alter vascular tone include the osmolarity of extracellular fluid and its concentration of CO2, K+, H+, O2 and adenosine, and were known to modifies the oxygen and nutrient requirement by local tissue. (Orgul S. Et. al, 1999). In the retina there is general agreement that blood flow adapts in response to different conditions of light and darkness including diffuse luminance flicker. The measurement were taken before, during and after stimulation with diffuse luminance flicker. Flicker light is a flashes of light at wavelength below 550nm and retinal irradiance of 140 ÂµW/cm. The study clearly demonstrates that diffuse luminance flicker increases optic nerve blood flow but shows no effect on choroidal blood flow, thus choriodal blood flow appears to be work independently of the alteration in retinal metabolism. (GarhÇ˜fer G. et. al, 2002). Myogenic appear to actively contribute to the autoregulation of retinal blood flow. (Rosa R.H., 2004). In ocular tissue, autonomic nervous system contributes extensively to the retrobulbar and choroidal circulatory system, but the retinal and ONH vasculature still lack direct innervations. (Funk 1997). As for sympathetic stimulation, it only provides indirect influence on ONH perfusion neurogenic contribution to the vascular responce is minimal. (Harris et. al, 2003).
According to Mchedlishvili 1981, vasospasm can cause a reduction in luminal diameter and respective the blood flow. (Mchedlishvili 1981). Consequent ischemia surrounding tissue may originate from vasoconstriction or insufficient dilatation of the microcirculation. Dysregulation of the blood flow can lead to an over- or underperfusion. As for long term damage can come from a steady overperfusion of the blood flow. While under perfusion can lead to tissue atrophy and cell infarction. Systemic regulation can be primary or secondary of nature. Autoimune disease such rheumatoid arthritis, gaint cell arteritis, systemic lupus erythematodes, multiple sclerosis, colitis ulcerosa or Chrohns disease are categorize as a secondary dysregulation. According to Gasser P. (1991), vasospasm are not only occur in Raynaud's disease, migraine, Prinzmetal's variant angina, visual filed defects and partially in low-tension glaucoma, but may also be involved in pathogenesis of Crohn's disease. In other words, vasospasm does occur in the eye. Increase of endothelin-1 circulation leads to a reduction of blood flow in both choroid and optic nerve head in secondary vascular dysregulation. The primary vascular dysregulation has a little influence on ocular blood flow but still interferes with autoregulation. This seems to be a relevant component in pathogenesis of glaucomatous optic neuropathy. (Greishaber M.C. et. al, 2007; Emre M. Et. al, 2004). Normal tension glaucoma (NTG) reported twice female than male and considered to be an independent risk factor for visual field loss progression in NTG. (Orgul S. Et. al, 1994; Drance S. Et. al, 2001). Estrogen is known to have vasodilatory effects in systemic circulation. Decrease in estrogen levels during menopause may therefore complicate or contribute to ocular pathologies as estrogen receptors are found in both retinal and choroidal tissue. Therefore, the susceptibility in females may due to falling to estrogen level under post-menopause. (Seisky et. al, 2008).
Vasospasm has been associated with glaucoma, but the mechanism have not been clearly elaborated. A potent endogenous vasoconstrictor, endothelin (ET)-1 were increase in patient with glaucoma compared to normal subject. They also found that glaucoma patient with acral vasospasm, more likely to show deterioration in visual fields after cooling than patient without acral vasospasm. In other words, glaucoma patient with evidence of vasospasm have the risk of worsening visual fields under cooling induced than nonvasospastic patients. (Nicolela et al 2003). ///// This suggests that vasospasm may manifest itself in clinically relevant glaucomatous deterioration in certain individuals. Migraine, often characterized as a vasospastic disorder, is more commonly found in females and has a well documented association with NTG (Cursiefen et al 2000). It has been demonstrated as a risk factor for the progression of visual fi eld loss, suggesting a common underlying vascular pathology for both conditions (McKendrick et al 2000). Also frequently associated with vasospasm, low blood pressure is a reported risk factor for glaucoma, but if systemic hypotension is secondary to vasospasm or an unrelated phenomenon remains uncertain (Kaiser et al 1993b; Gass et al 1997;Gasser 1998; Pache et al 2003). It has been shown that blood pressure variations away from normal physiologic nocturnal dips are correlated with vasospasm, OAG, and NTG (Werne et al 2008). The failure of ocular blood flow to remain constant during physiological challenges may manifest itself as ocular vasospasm or represent primary vascular dysregulation during vasospastic episodes.
Vasospasm is a transient phenomenon that is potentially reversible, allowing the restoration of steady-state perfusion. Due to its time-dependent nature, baseline blood flow measurements may not demonstrate any abnormalities compared with controls (Gugleta et al 2003). Therefore, the use of a provocation test to unmask underlying vascular dysregulation has been proposed in ocular hemodynamic measurements (Gugleta et al 2005). Harris and colleagues (1994) showed that NTG patients had significantly lower ophthalmic artery blood flow velocities and higher vascular resistance than controls. The differences between NTG and controls were reversed during elevated CO2 breathing, suggesting the presence of a reversible vasospasm in the NTG cohort (Harris et al 1994). A study by Gugleta and colleagues (2005) found women with vasospasm demonstrated an inverse response pattern of choroidal and ONH blood gas perturbations compared with women without vasospasm. The authors suggest that vasospastic patients may have diminished autoregulatory capacity or increased responsiveness to CO2 in certain vascular beds. A differentiation of normal and abnormal blood fl ow regulation during blood gas perturbations and calcium channel blockers may demonstrate which persons are at greatest risk for vasospasm, impaired ocular blood flow and possibly OAG.
In summary, vasospasm is associated with multiple disease states including OAG with NTG patients and women appearing to be the most at risk for vasopastic contributions to disease processes. Vasospasm may result in fluctuations in ocular perfusion, ischemia, and/or reperfusion injury to the ocular tissues. Importantly, vasospasm may be reversible (treatable). The capacity of diagnostic testing for OAG risk using blood gas perturbations should be further explored, especially in patients that demonstrate a vasospastic propensity.
The vascular endothelium regulates the microcirculation through release of vasoactive factors, the most potent of which are the vasodilator nitric oxide (NO) and the vasoconstrictor endothelin-1 (ET-1) (Adams 2006). Additional endothelium-derived activating compounds include prostacyclins, acetylcholine, bradykinin, and histamine (Flammer and Orgul 1998; Adams 2006). In endothelial cells, NO synthase (NOS) catalyzes the conversion of L-arginine to NO and L-citrulline. NO released from endothelial cells directly stimulates the surrounding vascular smooth muscle to promote vasodilation (Toda and Nakanishi-Toda 2007). It is known that NO activity contributes to ocular autoregulation
and can protect the endothelium and nerve fiber layer against pathologic stressors implicated in glaucoma, ischemia, and diabetes (Toda and Nakanishi-Toda 2007). Decreased levels of cyclic GMP, an indicator of NO activity, have been demonstrated in the plasma and aqueous humor of
glaucoma patients, with corresponding lower systolic and diastolic ophthalmic artery blood fl ow velocities of NTG patients (Laude et al 2004). There is evidence that enhanced ET-1 vasoconstriction is involved in the pathology of such conditions as hypertension, heart failure, myocardial infarction, renal failure, and secondary vasospastic disorders (Ortega and de Artinano 1997). A number of studies have investigated the role of ET-1 in glaucoma. ET-1 has been shown to decrease blood flow
to the anterior optic nerve when directly applied to this region (Orgul et al 1996). Aqueous humor levels of ET-1 are reportedly elevated in HTG (Noske et al 1997) and one study demonstrated a significant elevation of plasma ET-1 in HTG when the subjects were moved from the supine
to upright position (Kaiser et al 1997). Grieshaber and Flammer (2005) suggest that the elevation of ET-1 in glaucoma represents an epiphenomenon rather than a distinctive mechanism. They point
to the observation of significantly elevated ET-1 levels in vasospastic and systemic diseases such as multiple sclerosis, rheumatoid arthritis, fibromyalgia, and Susac syndrome. Although a pale ONH is often associated with these diseases, glaucoma does not occur more frequently in these patients
than in the average population. This suggests that ET-1 upregulation may be secondary to repetitive perfusion insufficiency and damage occurring not only in the ONH, but also subclinically in multiple organs (Waldmann et al 1996; Grieshaber and Flammer 2005).
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2.4 Ocular Blood Flow & Visual Field
Plange et al found that asymmetric glaucomatous visual field loss was associated with asymmetric flow velocity in cetral retinal and ophthalmic arteries in POAG patients. (Plange et al, 2006). In addition, Zeitz et al found glaucoma progression to be associated with decreased blood flow velocities in the short posterior ciliary arteries. (Zeitz et. al, 2006). Zink et al Found an association between lower optic nerve laser Doppler blood volume measurement and glaucomatous visual field progression. (Zink et al, 2003). Galassi F. Et. al (2003), reported that patient with a stable visual field had a higher diastolic velocity and a lower resistivity index in the ophthalmic artery (OA) compared to those with a deteriorating visual field during the study. Patient with a vascular resistance greater than 0.78 in the OA had 6-times the risk of visual field deterioration. Following research by Martinez et. al (2005), suggesting a correlation between RI greater than 0.72 in the OA and increased VF progression over a period of 3 years. Independent of the progression rate of glaucomatous visual field damage statistically correlates with retrobulbar hemodynamic variables as the faster rate in progression of glaucomatous damage, a lower baseline end diastolic blood flow velocity in the central retinal artery. (Satilmis M. et. al, 2003). The evaluation of glaucoma damage were also conducted between the extent of glaucoma damage and optic nerve blood flow, found that when both of the eyes have glaucoma, the hemidisk with greater damage showed significantly lower blood velocity than the hemidisk with less damage. (Lam A. et. al, 2005). This study provides additional evidence that impaired optic nerve circulation is associated with the extent of glaucomatous pathology. Sato and associates reported that reduction of capillary blood flow at neuroretinal rim in normal tension glaucoma patients was associated with regional visual field loss.
Sclera buckling for a rhegmatogenous retinal detachment (RPD) were also found to cause a reduction in blood flow at neuroretinal rim. Upon removing the buckle, the blood flow were improved to normal levels and a further worsening of the visual field was not detected. These result suggest that an encircling of sclera buckle may impair choroidal circulation and lead to visual field defects similar to eyes with normal tension glaucoma. (Sato E.A. et. al, 2008). Research done by Vassilos and associates with 13 male & 3 female with bilateral carotid stenosis, found that postoperatively peak systolic velocity had significantly improved in all vessels examined in the carotid that was operated on, but only in the OA and short posterior cilary artery in the fellow side.
Ocular blood flow deficits may therefore represent either a primary insult or are secondary to vascular regulatory dysfunction during diurnal fluctuations in vascular risk factors in certain OAG patients (Grieshaber and Flammer 2005).