BACKGROUND Ocular pulse amplitude (OPA) is reduced in normal tension primary open angle glaucoma (NTP) patients when compared with healthy age matched controls (CTL) while increased OPA appears to protect ocular hypertensive patients from visual field loss. If NTP is accompanied by vasospasm, as in roughly half of the primary open angle glaucoma (POAG) population (independent of intraocular pressure, IOP), calcium channel blockers increase OPA and thus stabilise visual fields in these patients. Current glaucoma drugs reduce IOP but do not activate (compromised) ocular perfusion.
METHODS The influence of dorzolamide, a topical carbonic anhydrase inhibitor in standard dosage (three times daily, one eye) on OPA, IOP, blood pressure, and heart rate was investigated in a randomised, prospective, masked clinical trial assessing the acute effects of dorzolamidev placebo before and 2 days after application in 33 cataract patients with (n = 14) and without (n = 19) high tension POAG (HTP) who provided informed consent.
RESULTS Following application of dorzolamide (D) IOP (mm Hg, mean (SEM)) in HTPD (20.2 (0.5)/16.3 (0.5)) and in CTLD (16.0 (0.5)/12.3 (0.5)) was highly significantly (p <0.001) reduced and was significantly (p<0.03) reduced in vehicle (V) treated eyes (HTPV: 20.3 (0.4)/19.0 (0.4)) and CTLV: 15.8 (0.4)/14.9 (0.3)) when compared with respective baseline measurements. OPA (mm Hg) in HTPD (2.1 (0.1)/2.5 (0.1)) and CTLD (2.2 (0.1)/2.6 (0.2)) eyes was significantly (p<0.05) increased and unaffected in vehicle treated eyes when compared with respective baseline measurements. Systemic perfusion variables were also unchanged.
CONCLUSION Dorzolamide increased OPA in HTP and CTL. Drugs stimulating OPA may improve prognosis of POAGs.
- ocular pulse amplitude
- primary open angle glaucoma
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A reduction of ocular pulse amplitude (OPA) in primary open angle glaucoma (POAG) patients with normal tension (NTP)1-4 independent of vasospasm4 seems to correlate with progression of visual field loss,5 whereas increased OPA appears to protect ocular hypertensive patients from visual field loss and glaucomatous disc cupping, which we interpret as a protective mechanism or adaptive change to prevent hypoperfusion induced damage to optic nerve fibre layers.1 2
OPA is the measure of a bolus of blood entering the eye, the maximum and minimum measurements reflect, in keeping with the cardiovascular definitions of systolic and diastolic blood pressures, systolic and diastolic intraocular pressures (IOPs), respectively,6which illustrate the pulsatile component of intraocular blood flow.7
According to Alm8 total ocular perfusion as determined in monkeys is approximately 800 mg/min, the choroid contributes 677 mg/min (85%), the iris 8 mg/min (1%), the ciliary body 81 mg/min (10%), and the retina 34 mg/min (4%). The pulsatile component of the choroidal perfusion as investigated by colour coded Doppler ultrasonography is approximately 70%.9
The ocular blood flow (OBF) system (OBF Labs Ltd, Wilts), a highly sensitive pneumotonometer linked to a data acquisition unit measures IOP (mm Hg) non-invasively with a collection rate of 200 Hz, allowing accurate, non-invasive, and reproducible10 11measurements of OPA with minimal disturbance to the eye.
Ocular blood flow was not calculated from OPA measurements because extraocular factors are involved (for example, pulse rate and posture) and, in our opinion, the underlying assumptions (pressure/volume relation in the living human eye) as well as the lack of relevant intraocular factors (width of pulse amplitude, scleral rigidity, axial length) and the software provided with the OBF system are not adequately documented to calculate blood flow from the pulse data.
Even if the goal of current glaucoma therapy (high tension POAG, HTP: IOP <20 mm Hg; NTP: IOP <15 mm Hg) is reached, progression of visual field loss and optic nerve head cupping continue in many subjects, mandating that therapeutic concepts independent of or in addition to reducing IOP be considered. One of these is increasing ocular blood flow.
Systemic carbonic anhydrase inhibitors (CAIs) such as acetazolamide are increasingly being used as vasodilators, equally effective as carbon dioxide, to detect cerebrovascular vasomotor reserve capacity and increase cerebral blood flow and oxyhaemoglobin in patients with chronic cerebrovascular disease.12-14 Thus, CAI has been shown to improve visual function probably by increasing ocular pulse volume and pulsatile ocular blood flow15 induced by a reduction in pH of blood and tissues.16
The long term use of this systemic drug is limited by side effects such as electrolyte imbalance, fatigue, depression, gastrointestinal complaints, occurrence of renal stones as well as blood dyscrasias.
The present study was designed to evaluate for the effect of dorzolamide hydrochloride (Trusopt, Merk & Co Inc, West Point, PA, USA) a topical CAI on OPA in HTP patients and non-glaucomatous controls (CTL).
Materials and methods
Sixteen CTL subjects (nine male, seven female), 46–68 (mean 58.0) years of age with no known ocular disease other than cataract, who showed no visual field defects and/or disc alterations and had IOPs < 21 mm Hg and 12 patients with bilateral HTP and cataracts (five male, seven female), 42–71 (mean 56.3) years of age, each undergoing cataract surgery received dorzolamide in the one eye undergoing cataract surgery in standard dosage (three times daily), hydroxyethylcellulose (three times daily) as a placebo in the contralateral control eye, and complied with the protocol of this study. Additionally, both eyes of HTP and CTL patients received gentamicin eye drops six times per day as preoperative antibiotic prophylaxis.
The HTP and CTL patients had no history of systemic hypertension, diabetes mellitus, elevated cholesterol, neurological deficits, or typical migraine headache, and had no known eye disease other than the category selected for or ocular surgery including laser of any kind and remained on their systemic therapy. The HTP patients chosen had a history of pretreatment IOPs >21 mm Hg, had typical glaucomatous disc cupping (disc size 1.8–2.3 mm2, C/D ratio >0.6) with corresponding visual field loss, remained on their long standing, unaltered (>3 months) ocular hypotensive therapy, and additionally received dorzolamide.
Only HTP patients on either adrenaline (1%) or timolol (0.5%), eye drops which have been shown to reduce IOP, but not to affect OPA in our human studies1 2 17 were allowed in this trial; patients continued these medications in their usual dosage during the course of the trial.
In this study dorzolamide (2%) and hydroxymethylcellulose as a vehicle were each applied three times daily to either eye of each patient for 2 days.
In addition to pneumotonometric values, IOP was measured by Goldmann applanation tonometry. Brachial artery pressures were measured non-invasively (Riva-Rocci) using a blood pressure cuff and a stethoscope. Heart rate (HR) was measured manually using a stopwatch. Applanation IOP, systolic (BPsyst) and diastolic (BPdiast) blood pressures (BP), and HR were taken before OPA measurements.
All OPA and IOP readings for this study were taken by the same examiner, who performed these measurements masked to which eye was drug treated.
Measurements of patients were taken before and during dorzolamide treatment with the patient in a seated position at the same time of day with respect to pre-dorzolamide measurements and 2 hours after drug and vehicle application.
The protocol was accepted by the institutional review board of the University of Giessen and informed consent was obtained from each patient following complete explanation of the procedure.
All data were normally distributed and represent arithmetic mean (plus or minus SEM); Student’s paired two tailedt test was used for statistical analysis. Measurements were performed on both eyes of each subject. One eye received dorzolamide, the other eye was vehicle treated. Pretreatment values did not differ significantly in treated versus untreated HTP and CTL groups, respectively. Data before treatment were compared with data from respective groups after 2 days of dorzolamide treatment before surgery. The level of significance was 5%—that is, p<0.05 was considered significant.
Following administration of dorzolamide (D) IOP (mm Hg) was significantly (p<0.001) reduced in drug treated HTP (HTPD) patients, from 20.2 (0.5) to 16.3 (0.5), reflecting a 19.3% reduction of IOP. After the administration of the same topical drug using the protocol mentioned above IOP was significantly (p<0.001) reduced in drug treated CTL subjects (CTLD), from 16.0 (0.5) to 12.3 (0.5), reflecting a 23.1% reduction of IOP (Fig 1). In vehicle treated HTP (HTPV) IOP was significantly (p<0.03) reduced from 20.3 (0.4) to 19.0 (0.4), corresponding to a 6.4% reduction of IOP (Fig 1). In vehicle treated CTL (CTLV) IOP was significantly (p<0.03) reduced from 15.8 (0.4) to 14.9 (0.3), reflecting a 5.7% decrease in IOP (Fig 1).
Administration of dorzolamide caused a significant (p<0.05) increase of OPA (mm Hg) in HTPD from 2.1 (0.1) to 2.5 (0.1), reflecting a 19.1% increment (Fig 2). After administration of the same topical drug using the protocol mentioned above in CTLD, OPA increased from 2.2 (0.1) to 2.6 (0.2), reflecting an 18.2% rise (Fig 2). Following application of the vehicle using the protocol mentioned above OPA was unaffected in HTPV (2.1 (0.1)/2.1 (0.1)) and CTLV (2.2 (0.1)/2.2 (0.1)) eyes when compared with respective measurements before dorzolamide treatment (Fig2).
Systemic perfusion variables were not significantly (p>0.05) altered in HTP and CTL subjects when compared with respective baseline measurements (Table 1).
In treated eyes IOP reduction following application of topical dorzolamide 2% three times daily was 19.3 and 23.1% in HTP and CTL, respectively, which is in the range of other clinical trials (18–30%)18-22; in the same eyes OPA increased 19.1 and 18.2% in HTP and CTL subjects, respectively, which correlates well with the IOP reduction suggesting an IOP/OPA interdependence in this range of IOPs.
Following the concept that IOP exerts a compressive force on the choroid, a low resistance vascular structure,9 a reduction of this force should increase OPA—provided the drug tested has no direct effect on ocular or systemic vascular systems. Surprisingly, vehicle treated contralateral control eyes showed a significant but less pronounced reduction in IOP, also noted in other primates23 which may be due to a systemic effect of dorzolamide; these eyes showed no change in OPA pointing to factors other than IOP to influence ocular haemodynamics in this range of IOPs.
Systemic perfusion variables being unaltered, Kielet al 24 25 noted a negative correlation for IOP/choroidal blood flow <25 mm Hg in rabbits, postulating a myogenic regulation mechanism in the choroid reaching its adaptive maximum at 25 mm Hg.
Also, most other current glaucoma drugs reduce IOP but do not increase OPA1 2 17 which may demonstrate a relative negative effect of these drugs on the choroidal vasculature and/or a compensatory mechanism for IOP changes in this vascular system in humans also.
A review of the literature shows contradictory results regarding the role of timolol with respect to ocular circulation. Timolol prevents a compensatory sympathetic reflex by blocking vascular β2and α receptors and thus may increase peripheral resistance which in turn may affect OPA, but this effect was not noted in our topical glaucoma drug studies.1 2 17 Trew and Smith26 noted no improvement in pulsatile ocular blood flow (POBF), a variable not calculated in our studies (see earlier), following application of timolol 0.25% in HTP patients whereas following application of timolol 0.5% Boles-Careniniet al 27 showed a significant decrease of POBF; Martin and Rabineau28 noted a reduction of the mean retinal arterial diameter. In our studies the topical glaucoma drugs at the concentrations used in this study reduced IOP but did not affect OPA in ocular hypertensive volunteers1 2and native cynomolgus monkey eyes.17
Dorzolamide additively increases the IOP lowering effect of timolol29 30; although the pharmacological interactions for adrenaline and dorzolamide are not yet described, owing to their different pharmacological modes of action (adrenaline, a direct α and β sympathomimetic, reduces IOP by its α adrenergic vasoconstrictive effect on ciliary body capillaries,31 and α and β adrenergic, probably cAMP mediated,32 increase in trabecular33 and uveoscleral outflow34 35), it seems reasonable to also assume an additive IOP lowering effect.
Interactions of dorzolamide with timolol and/or adrenaline affecting OPA in the HTP group are conceivable but unlikely, owing to their different pharmacological modes of action and lack of effect of timolol and adrenaline on OPA when applied as monotherapy.1 2 In the limited study reported here there was no significant difference in IOP reduction, OPA increase, and systemic perfusion variables in dorzolamide/timolol v dorzolamide/adrenaline HTP groups.
Measurements of IOP and OPA made during the course of development of the cynomolgus monkey glaucoma model gave the unexpected result that OPA does not decrease when IOP increases in the lasered eye, but instead it increased in the contralateral unlasered eye which responds with a higher OPA. This finding remains consistent after full development of the glaucoma. This result may seem paradoxical but is understandable if a higher IOP in one eye causes a systemic or bilateral compensatory regulation which is more manifest in the eye with normal IOP than in the lasered eye with the increased IOP.17
This postulate is also in line with indications from studies in human subjects that glaucomatous eyes may have an impaired compensatory OPA response to IOP elevation,1-4 17 which may exhibit an impeded functional reserve in the choroid and may reflect a primary decrease in choroidal capacity,1 2 4 decreased perfusion pressures as measured by oculo-oscillodynamography,38and/or reduced ophthalmic artery perfusion.39 40
Physical exercise in normal healthy volunteers significantly (p<0.05) increased heart rate (208.0%), systolic blood pressure (20.4%), and ocular perfusion pressure (265.0%), and significantly (p<0.05) reduced IOP (32.3%) and diastolic blood pressure (17.0%). OPA was unchanged3 again suggesting functional isolation—that is, significant autoregulatory capacity of the choroidal vasculature in the normal range of IOPs of healthy volunteers, which appears to compensate for a significant increase in pulse pressure and the significant reduction in IOP.
Although we cannot rule out with absolute certainty an IOP/OPA interdependence for the IOP range examined, these results make it very unlikely that a change in IOP may account for the increase in OPA following application of dorzolamide.
Kitazawa et al 5 demonstrated visual field improvements in six of 25 NTP patients following application of nifedipine, a calcium channel blocker, vasodilator, and systemic antihypertensive agent which is successfully used in vasospastic disorders. Netland et al 41 observed a significant decrease in the progression of NTP but not in HTP over a 3.4 year period.
NTP patients with a vasospastic reaction treated with nifedipine, showed a significant (p<0.001) increase in OPA while NTP patients without a vasospastic reaction failed to show significant changes in OPA.4 The response to nifedipine in half of the NTP patients match the findings of Kitazawa et al 5 who demonstrated that half of their POAG patients independent of IOP suffer from vasospastic disorders.
An increase in OPA without affecting IOP3 might explain the stabilising effect of nifedipine on visual fields in NTP observed by Netland.41 This effect is probably due to the calcium channel blocker’s pharmacological mode of action. Calcium channel blockers primarily reduce arterial resistance by blocking calcium influx into the vascular smooth muscle cell42 and by inhibition of the endothelial vasoconstrictor endothelin-143 44 elevated in peripheral blood samples of NTP patients.45 Up to now calcium channel blockers were the only drugs known to increase OPA in a subgroup of glaucoma patients.3
CAIs are located in brain arteries46 and the capillaries of the choroid and retina.47 Inhibition of this enzyme, predominantly by a change in pH resulting in metabolic acidosis,16 reduces resistance in large cerebral arteries and thus dilates these vessels.46
The increase in OPA following application of a topical CAI may be a reflection of this effect on the choroidal vasculature and is in keeping with the positive haemodynamic effects of this drug on retrobulbar, retinal, and epipapillary circulation observed by Harriset al,48 is in line with similar findings reported for a systemic CAI,15 and confirms the theory for the CAI mode of action proposed by Pfeifferet al.19 They consider that an improvement in visual function following application of systemic CAIs is due to increased ocular perfusion as a result of acidification of blood and tissues.
Although the clinical aspects of POAGs, a syndrome of progressive optic neuropathy, characterised by an unphysiologically large cup/disc ratio with reduced retinal sensitivity, visual field defects, and additional psychophysical alterations,49 are known in detail, the exact pathogenetic mechanism(s) resulting in this specific form of optic nerve head damage remain(s) unknown, it has become evident that glaucoma is a multifaceted disease. Attention to IOP reduction remains important, but does not address all mechanisms present within many POAG patients. Future medication must also increase perfusion to the eye.
As with all medications for glaucoma therapy, the ability of topical CAIs and other (selectively ocular) vasodilators to preserve visual function must be assessed in large studies performed over many years. Nevertheless, the limited study reported here indicates that vasoactive drugs may have potential in the specific treatment of POAG patients with reduced OPA.
Financial support: None.
Proprietary interest: None.
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