Pattern electroretinogram (PERG) and pattern visual evoked potential (PVEP) in the early stages of Alzheimer's disease.

Alzheimer's disease (AD) is one of the most common causes of dementia in the world. Patients with AD frequently complain of vision disturbances that do not manifest as changes in routine ophthalmological examination findings. The main causes of these disturbances are neuropathological changes in the visual cortex, although abnormalities in the retina and optic nerve cannot be excluded. Pattern electroretinogram (PERG) and pattern visual evoked potential (PVEP) tests are commonly used in ophthalmology to estimate bioelectrical function of the retina and optic nerve. The aim of this study was to determine whether retinal and optic nerve function, measured by PERG and PVEP tests, is changed in individuals in the early stages of AD with normal routine ophthalmological examination results. Standard PERG and PVEP tests were performed in 30 eyes of 30 patients with the early stages of AD. The results were compared to 30 eyes of 30 normal healthy controls. PERG and PVEP tests were recorded in accordance with the International Society for Clinical Electrophysiology of Vision (ISCEV) standards. Additionally, neural conduction was measured using retinocortical time (RCT)--the difference between P100-wave latency in PVEP and P50-wave implicit time in PERG. In PERG test, PVEP test, and RCT, statistically significant changes were detected. In PERG examination, increased implicit time of P50-wave (P < 0.03) and amplitudes reductions in P50- and N95-waves (P < 0.0001) were observed. In PVEP examination, increased latency of P100-wave (P < 0.0001) was found. A significant increase in RCT (P < 0.0001) was observed. The most prevalent features were amplitude reduction in N95-wave and increased latency of P100-wave which were seen in 56.7% (17/30) of the AD eyes. In patients with the early stages of AD and normal routine ophthalmological examination results, dysfunction of the retinal ganglion cells as well as of the optic nerve is present, as detected by PERG and PVEP tests. These dysfunctions, at least partially, explain the cause of visual disturbances observed in patients with the early stages of AD.

Introduction

Alzheimer’s disease (AD) is a progressive neurodegenerative disorder and one of the most common causes of dementia worldwide. It is estimated that in Europe alone, the number of the dementia sufferers is about 6.4%—most of them, patients with AD (4.4%) [1]. Due to the aging population, the number of patients with AD is on the increase and this contributes to a wider public health problem. The results of Mendez et al. [2] suggest that 43% of patients with AD have complex visual complaints. These patients require a proper diagnosis and suitable treatment, and the need for earlier diagnosis to slow the progression of the disease is undisputed.

Initially, AD symptoms are discreet and generally relate to memory deficits. However, in some cases, AD can begin with visual disturbances, including problems with reading, blurred vision, and vague complaints of poor vision. Such patients may have normal routine ophthalmological examination results including normal visual acuity and normal fundus [3-7]. The results of some studies suggest that in patients with AD, optic nerve degeneration, and loss of retinal cells, specifically disappearance of ganglion cells and their axons is evident [8-11]. In the brain of patients with AD, the characteristic features are beta-amyloid deposits and neurotransmitter’ production disturbances, mainly decreased levels of acetylcholine. Beta-amyloid deposits were also found in the eye [12, 13], and acetylcholine is crucial to proper functioning of retinal cells [14].

Potential value in diagnosis of visual abnormalities in AD may be provided by electrophysiological studies of the retina and optic nerve such as pattern electroretinogram (PERG) and pattern visual evoked potential (PVEP) tests. These examinations measure the bioelectrical activity of retinal ganglion cells and the optic nerve. To date, the available results of PERG and PVEP tests in patients with AD are inconclusive. Although abnormalities in PERG and in PVEP tests have been reported in patients with AD [15-21], normal PERG and PVEP tests results were also observed [15, 21–25].

In some PERG examinations, amplitude reduction was evident [15, 16]. Parisi et al. [17] showed a significant increase in latencies of N35-, P50-, and N95-waves and reduction in their amplitudes. Additionally, P50-wave latency increase and amplitude reduction in P50- and N95-waves were correlated with a statistically significant reduction in nerve fiber layer thickness, as measured by Optical Coherence Tomography (OCT). In PVEP examination, a latency increase in the P100-wave was observed by Pollock et al. [19], Kergoat et al. [21], and Partanen et al. [18]. The described studies were performed in patients who were at different stages of AD, and most of them examined small numbers of patients. The aim of the current research is to evaluate retinal and optic nerve bioelectric function in patients only in the early stages of AD by means of PERG and PVEP tests.

Subjects and methods

Thirty patients in the early stages of AD (20 [66.7%] women and 10 [33.3%] men), aged 54–83 (mean 72.9 ± 6.8), were diagnosed in the Neurology Department of the Pomeranian Medical University in Szczecin, Poland.

Each patient with AD underwent neurologic examination including magnetic resonance imaging (MRI). All patients met the diagnostic criteria of probable AD according to the National Institute of Neurological and Communicative Disorders and Stroke and the Alzheimer’s Disease Association (NINCDS-ADRDA) [26]. The inclusion criteria for the early stages of AD were as follows: minimal cognitive disturbances in accordance with the neurologic tests and the Mini Mental State Examination (MMSE) [27] score above 21 points. Patients were diagnosed as having AD from 6 months to 2 years. The ocular inclusion criteria were as follows: taking patient’s history, visual acuity >0.8 (Snellen chart), normal intraocular pressure, normal kinetic visual field, no changes in anterior and posterior segment of the eye, and normal color vision. Patients with systemic disorders with known influence on the function of retina and optic nerve as well as with poor cooperation were excluded.

PERG and PVEP tests were performed in all patients (30 eyes—always left). Additionally, the measurement of retinocortical time (RCT)—a parameter described for the first time by Celesia et al. [28, 29]—was obtained to provide more precise information regarding neural conduction in the postretinal visual pathway. PERG and PVEP examinations were recorded with the RetiPort (Roland Consult) system, in accordance with the ISCEV PERG and PVEP standards [30-33].

At the beginning of the study, 10 patients with AD had the PERG and PVEP tests performed twice in two separate sessions for checking the reproducibility of measurements. Reproducible results were obtained. Variability was determined by calculating the coefficients of variation (CV) for PERG and PVEP tests. Additionally, for each parameter, statistical comparisons of mean values and variances were performed. Student t-test and test for two variances for dependent two samples were used. There were no statistical differences between compared parameters mentioned earlier. For all measured parameters, for which the statistically significant abnormalities between patients with AD and control group were obtained, the intersessions variability did not exceed 10%—Table 1.

Table 1

Early stages of Alzheimer’s disease—analysis of the mean CV for parameters of PERG and PVEP tests (n = 10)

Parameter	Measurement	Min	Max	x ± SD	CV [%]	P value
IT P50 [ms]	I	47.00	56.00	51.30 ± 3.09	6.03	NS
	II	48.00	56.00	51.6 ± 2.32	4.49
A P50 [μV]	I	2.63	3.90	3.61 ± 0.36	9.99	NS
	II	2.91	4.39	3.84 ± 0.38	9.96
A N95 [μV]	I	3.82	5.42	4.29 ± 0.44	9.73	NS
	II	3.58	5.18	4.28 ± 0.39	9.03
L P100 [ms]	I	106.00	120.00	111.0 ± 4.81	4.33	NS
	II	107.00	119.00	110.0 ± 4.12	3.72
L P100 [ms]	I	105.00	129.00	122.00 ± 7.59	6.22	NS
	II	107.00	128.00	121.00 ± 7.20	5.91

n number of eyes, x arithmetic mean value, SD standard deviation, P significance level, NS not significant, I first examination, II second examination, IT implicit time, A amplitude, L latency

PERG test

Preparation of the patient: pupils were undilated, appropriate refractive error correction in relation to the eye-screen distance, binocular stimulation, and monitoring with a TV camera (to stop the stimulations when frequent blinking or fixation loss) was carried out.

Parameters of the pattern stimulation were as follows: 21″ CRT monitor with a frame rate: 75 fps was used, a black and white reversing checkerboard was presented to the patient with a check size: 0.96°, luminance for the white elements: 120 cd/m2, contrast: 97%, temporal frequency: 4.7 rev/s (2.35 Hz), and central fixation was used.

Electrodes: thread DTL electrodes were used as active and a gold disk placed at the ipsilateral outer canthi as reference, with ground—gold disk—electrode placed on the forehead (Fpz).

Parameters of the recording system were as follows: filters: 1–100 Hz, switched off notch filters, sweep time: 250 ms, artifact reject threshold: 50 μV, averaging: 200 sweeps. Two consecutive waveforms were recorded, off-line averaged, and then analyzed.

Analysis of PERG parameters: amplitude and time of the P50- and N95-waves with manual correction to the automatic cursor placement were analyzed.

PVEP test

Preparation of the patient: pupils were undilated, appropriate refractive error correction in relation to the eye-screen distance, monocular stimulation, monitoring with the TV camera (to stop the stimulation when frequent blinking or fixation loss) was used.

Parameters of the pattern stimulation were as follows: 21″ CRT monitor with a frame rate: 75 fps was used, a black and white reversing checkerboard was presented to the patient with a check size: 1°4′ and 16′, luminance for the white elements: 120 cd/m2 (mean luminance 55 cd/m2), contrast: 97%, temporal frequency: 2 rev/s (1 Hz), and central fixation was carried out.

Electrodes: active—gold disk electrode placed on the scalp over the visual cortex at Oz with reference—gold disk electrode placed at Fz; ground—gold disk electrode placed on the forehead at Fpz. The electrodes were placed relative to bone landmarks according to the international 10/20 system [34].

Parameters of the recording system were as follows: filters: 1–100 Hz, switched off notch filters, sweep time: 300 ms, artifact reject threshold: 50 μV, averaging: 100 sweeps. Two consecutive waveforms were recorded, off-line averaged and then analyzed.

Analysis of PVEP parameters: amplitude and time of the P100-wave with manual correction to the automatic cursor placement were analyzed. Furthermore, in order to evaluate the bioelectrical function of macular vs more peripheral regions of the retina, differences between amplitudes of P100-wave in patients with the early stages of AD and control subjects after simulation with the small (16′) and large (1°4′) check stimuli were measured. The same comparisons were made between latencies of the P100-wave.

Retinocortical times (RCTs) were also compared, that is the difference between latency of P100-wave (16′ checks—RCT 1 and 1°4′ checks—RCT 2) and implicit time of the P50-wave, following the methods described by Celesia et al. [28, 29].

Values of all parameters of patients with AD were compared with the values for the control group consisting of 30 eyes (always left) of 30 healthy individuals matched for age, sex, and refractive errors with AD patients.

The research was conducted in accordance with the principles of the Declaration of Helsinki, informed consent was obtained, and the protocol was approved by the local Independent Ethics Committee.

The Shapiro–Wilk test was used to evaluate compatibility with normal distribution of analyzed electrophysiological parameters. The PERG and PVEP parameters in eyes of patients with AD and eyes of the control group were compared in the following way: (1) for normally distributed data, the arithmetic mean and standard deviation was applied, and Student t-test was used (2) for abnormally distributed data, minimum–maximum value and median was used and evaluated with the Mann–Whitney U test. The results of PERG and PVEP tests were considered normal when they included between mean and ±two standard deviations (x ± 2SD) for normally distributed data or 2.5 and 97.5 percentiles for abnormally distributed data. The significance level of PERG and PVEP parameters was <0.05. For statistical calculations, the number of eyes tested was used, rather than the number of subjects.

Results

In the group of patients with AD, 33.0% (10/30) had visual problems in the form of difficulty with reading, writing, or undefined visual disturbances, although their optimal visual acuity for near vision was J1.0 (Jaeger charts).

The statistical analyses of PERG and PVEP results are shown in Tables 2, 3, 4, 5, 6, 7. In the eyes of patients with AD, PERG test revealed statistically significant implicit time increase in the P50-wave (P < 0.03) and reduced P50- (P < 0.0001) and N95-wave (P < 0.0001) amplitudes in comparison with normal subjects (Table 2). Analysis of individual results of PERG parameters revealed abnormalities in 20.0% (6/30), 50% (15/30), and 56.7% (17/30) of the eyes, respectively. In the eyes of patients with AD in the PVEP test (1°4′ and 16′), a statistically significant increase in latency of the P100-wave (P < 0.0001) was observed (Tables 3, 4). Analysis of individual results in PVEP parameters revealed abnormalities in 43.3% (13/30) and 56.7% (17/30) of the AD eyes, respectively.

Table 2

Early stages of Alzheimer’s disease—analysis of the mean amplitude and mean implicit time in PERG test in comparison with normal subjects

	Amplitude [μV]								P value
	AD				C
	Min	Max	x ± SD	Med	Min	Max	x ± SD	Med
P50	0.8	5.7	3.1 ± 1.4	2.9	2.2	8.2	4.9 ± 1.4	4.8	<0.0001*
N95	1.6	8.8	4.4 ± 1.8	4.0	3.8	11.9	7.1 ± 2.2	6.5	<0.0001**
N95/P50 ratio	0.6	2.8	1.5 ± 0.4	1.5	0.8	2.0	1.5 ± 0.2	1.5	NS

AD Alzheimer’s disease group, C control group, Min minimal value, Max maximal value, x arithmetic mean value, SD standard deviation, Med median, P significance level, NS not significant; * normal distribution, ** not normal distribution

Table 3

Early stages of Alzheimer’s disease—analysis of the mean amplitude and mean latency of P100 in PVEP test (1°4′) in comparison with normal subjects

	Amplitude [μV]								P value
	AD				C
	Min	Max	x ± SD	Med	Min	Max	x ± SD	Med
P100	0.8	3.5	1.9 ± 0.7	2.0	0.8	6.4	2.2 ± 1.4	1.8	NS

AD Alzheimer’s disease group, C control group, Min minimal value, Max maximal value, x arithmetic mean value, SD standard deviation, Med median, P significance level, NS not significant, ** not normal distribution

Table 4

Early stages of Alzheimer’s disease—analysis of the mean amplitude and mean latency of P100 in PVEP test (16′) in comparison with normal subjects

	Amplitude [μV]								P value
	AD				C
	Min	Max	x ± SD	Med	Min	Max	x ± SD	Med
P100	0.9	6.9	2.5 ± 1.4	2.1	0.6	8.7	2.5 ± 1.6	2.0	NS

AD Alzheimer’s disease group, C control group, Min minimal value, Max maximal value, x arithmetic mean value, SD standard deviation, Med median, P significance level, NS not significant, ** not normal distribution

Table 5

Difference between mean amplitude/latency of the P100-wave in patients with the early stages of AD and mean amplitude/latency of the P100-wave in normal subjects after stimulation with the small (16′) and large (1°4′) check stimuli

	Amplitude [μV]				P value
	Min	Max	x ± SD	Med
P100 (1°4′)	−5.4	2.3	−0.3 ± 1.7	−0.2	NS
P100 (16′)	−7.1	5.7	0.0 ± 2.2	−0.2

Min minimal value, Max maximal value, x arithmetic mean value, SD standard deviation, Med median, P significance level, NS not significant

Table 6

Early stages of Alzheimer’s disease—analysis of RCT 1 in comparison with normal subjects

RCT 1 [LP100 (16′)—LP50]								P value
AD				C
Min	Max	x ± SD	Med	Min	Max	x ± SD	Med
58.0	89.0	72.2 ± 6.4	72.5	48.0	78.0	64.2 ± 7.0	65.0	<0.0001*

RCT retinocortical time, AD Alzheimer’s disease group, C control group, Min minimal value, Max maximal value, x arithmetic mean value, SD standard deviation, Med median, P significance level, * normal distribution

Table 7

Early stages of Alzheimer’s disease—analysis of RCT 2 in comparison with normal subjects

RCT 2 [LP100 (1°4′)—LP50]									P value
AD					C
Min	Max	x ± SD	Med		Min	Max	x ± SD	Med
49.0	76.0	62.1 ± 6.5	60.5		42.0	70.0	55.1 ± 5.9	54.0	<0.0001*

RCT retinocortical time, AD Alzheimer’s disease group, C control group, Min minimal value, Max maximal value, x arithmetic mean value, SD standard deviation, Med median, P significance level, * normal distribution

The results of comparisons of the difference between mean amplitude/mean latency of the P100-wave in patients with the early stages of AD and in control individuals after stimulations of the small (16′) and large (1°4′) checks are shown in Table 5. Comparison of the P100-wave showed no statistically significant differences for the amplitudes or for the latencies.

In eyes of patients with AD, significant prolonged RCT (P < 0.0001) was observed in comparison with controls (Tables 6, 7). Analysis of individual results revealed abnormalities for RCT1 in 10.0% (3/30) and in RCT2 in 26.7% (8/30) of the AD eyes.

In Fig. 1, the frequency of abnormalities in PERG and PVEP tests in patients with the early stages of AD is shown.

Fig. 1

Early stages of Alzheimer’s disease—frequency of abnormalities in PERG and PVEP tests (A amplitude, L latency, RCT retinocortical time)

Examples of abnormal PERG and PVEP recordings in patients with AD are presented in Figs. 2, 3, 4. In Fig. 5, scatter-plots of PERG (amplitudes of P50- and N95-waves and implicit time of P50-wave) and PVEP (latencies of P100-wave) as a function of age are shown.

Fig. 2

PERG—P50-wave latency delay and reduced amplitudes of P50- and N95-wave in a patient with the early stage of Alzheimer’s disease (below) in comparison with the normal control (above)

Fig. 3

PVEP (1°4′)—P100-wave latency delay in a patient with the early stage of Alzheimer’s disease (below) in comparison with the normal control (above)

Fig. 4

PVEP (16′)—P100-wave latency delay in a patient with the early stage of Alzheimer’s disease (below) in comparison with the normal control (above)

Fig. 5

Early stages of Alzheimer’s disease—scatter-plot of PERG (amplitudes of P50- and N95-waves and implicit time of P50-wave) and PVEP (latencies of P100-wave) as a function of age (filled triangle Alzheimer’s disease group, filled square control group, horizontal line linear regression for AD group, black rectangle linear regression for control group)

Discussion

The results of our study strongly suggest, for the first time, that in patients with the early stages of AD, bioelectrical dysfunction of retinal ganglion cells and the optic nerve is present and this is registered by PERG and PVEP tests. Previously, some researchers [15-21] also reported abnormalities in PERG and PVEP tests in patients with AD but they considered different stages of this disease, with the exception of one study in which reduced amplitude of P100 in PVEP examination in patients with the early stages of AD was detected [20]. Furthermore, PERG and PVEP tests were usually performed on small numbers of patients and in which between-group comparisons were made.

It is worthwhile to note that recording of PERG and PVEP tests in patients with AD is not easy because of the possible secondary effects of defocus or other behavioral problems. To minimize these problems, in our study, appropriate selection of patients was made. We performed electrophysiological tests only in early stages of AD when patients had minimal disturbances of cognitive function and their cooperation was very good. PERG and PVEP examinations were recorded by the first author of presented manuscript who was familiar with the PERG and PVEP procedures and understood possible difficulties with cooperation in patients with AD.

In the present study, in patients with the early stages of AD, we noticed statistically significant abnormalities in PERG and in PVEP examinations (PERG: implicit time increase in P50-wave (P < 0.04), reduced amplitudes of P50- and N95-wave (P < 0.0001); PVEP (checkerboard: 1°4′ and 16′): latency increase in P100-wave (P < 0.0001). We also found statistically prolonged RCT (P < 0.0001). What is worthwhile to note, amplitude reduction of N95-wave in PERG examination, and latency increase of P100-wave in PVEP (16′) examination was found in more than 50% of analyzed AD eyes (Fig. 1).

N95-wave provides a measure of ganglion cells function but approximately 70% of the P50-wave is also generated by the ganglion cells [35]. The remaining 30% may be generated more distally [36, 37]. Amplitude reduction and implicit time shortening of the P50-wave are indicators of ganglion cells/optic nerve dysfunction. P50-wave implicit time increase is not a characteristic feature of optic nerve or ganglion cell disease [35, 37]—it may be seen in some maculopathies such as in macular edema [38].

In our group of patients with the early stages of AD, the observed reduced amplitude of N95-wave confirms the dysfunction of ganglion cells, whereas reduced amplitude and implicit time increase in P50-wave may be related to dysfunction, not only of the ganglion cells, but also of the outer layers of the retina in relation to the ganglion cells.

P-100 wave reflects the bioelectrical function of the optic nerve [37, 39]. Latency increase in P100-wave may be a subclinical feature of optic nerve dysfunction, and it may be detected without any pathological changes in routine ophthalmological examination [40]. The results obtained in patients with the early stages of AD showed increased latency of P100 and consistent with optic nerve dysfunction.

RCT may independently indicate neural conduction in the postretinal visual pathway [28, 29]. An example confirming this hypothesis is normal RCT but abnormal PERG and PVEP tests in patients with maculopathies. In this case, latency increase in PVEP test might be a consequence of abnormalities revealed in the PERG test.

In the group of patients with the early stages of AD, latency increase in P50- and P100-waves and prolonged RCT without any clinical signs of maculopathies were observed. Therefore, results of our study suggest that abnormalities in PERG/PVEP tests and in RCT could be connected not only with impaired neural conduction in the visual pathway including the optic nerve but also with dysfunction of the inner retinal layers. Previously, prolonged RCT was observed in neuropathies in the course of some diseases, e.g., in multiple sclerosis [29] and glaucoma [41]. According to Lam [39], different sizes of the check stimulus in PVEP test stimulate different parts of the retina. The large check stimulus elicits more parafoveal response and small check stimulus elicits a mainly foveal response. We also investigated the difference in PVEP examination between stimulation in the foveal and parafoveal region in patients with the early stages of AD.

Comparative analysis between amplitudes and latencies (Tables 4, 5) after large (1°4′) and small (16′) checks stimulation showed no statistically significant differences. Lack of regional differentiation in PVEP responses between the foveal and parafoveal part of the retina shows that in the early stages of AD, the optic nerve fibers can be evenly disturbed.

Most authors [2, 22] suggest that in patients with AD, visual disturbances are caused by neuropathological changes in the visual cortex. The results obtained in the current study show that visual disturbances in AD may also be related to the retinal ganglion cells and optic nerve dysfunction.

The possible causes of visual abnormalities mentioned earlier may be due to beta-amyloid and amyloid precursor protein (APP) deposits in the retina and optic nerve as well as retinal neurotransmitter deficits, mainly acetylcholine [42-44].

Some researchers observed the cytotoxic influence of aggregated beta-amyloid on neurons that express neurotransmitters, including acetylcholine [45]. Berisha et al. [8] observed that patients with early AD showed a significant thinning of retinal nerve fiber layer (RNFL), as measured by OCT. This may be connected with beta-amyloid aggregation and neuronal degeneration in the retina.

Acetylcholine plays an important role in the process of vision because it is essential for the proper functioning of retinal cells. Acetylcholine receptors are distributed predominantly in the inner retinal layers and also, but in smaller densities, in the outer layers of the retina [14, 46]. The indicators of dysfunction to the ganglion cells and to the outer layers of the retina are changes observed in N95-wave and in P50-waves of PERG examination, respectively.

Additional evidence suggesting that acetylcholine may play a role in observed abnormalities in patients with AD comes from a monkey study investigating the influence of acetylcholine level on PERG examination [47]. Administration of an acetylcholine precursor caused increased amplitudes in PERG test. In another studies, the effect of acetylcholine level was also explored on flash visual potentials (FVEP) recordings in healthy subjects [48, 49]. Administration of galanthamine—an inhibitor of the enzyme that breaks down acetylcholine—resulted in increased amplitudes [48] while the administration of the acetylcholine antagonist, scopolamine, caused reduction of P2-wave amplitude in FVEP test [49].

Thus, in patients with the early stages of AD, the dysfunction of retinal ganglion cells and the optic nerve as measured by PERG and PVEP examinations may be associated with the beta-amyloid deposits and neurotransmitters deficits.

In the current study group, visual complaints were observed in 1/3 (10/30) analyzed patients with the early stages of AD. Furthermore, the majority (7/10) had abnormalities in electrophysiological tests. In the remaining patients without visual symptoms, electrophysiological abnormalities are an indicator of conductive deterioration in visual pathway and can be a subclinical ocular feature of AD.

In the future, it would be worth to perform additional research in patients with the early stages of AD to include results of PERG responses to different check sizes (similar to the VEP recordings) and to correlate the data with OCT. In the present study in only a few patients in the early stages of AD, the OCT was performed, because the OCT equipment was available at the end of our research project. What is important, all these patients had normal OCT results, but abnormal PERG and PVEP examinations. Therefore, these examples suggest that dysfunction of the ganglion cells measured by electrophysiological tests precedes the structural changes in the ganglion cell layer. We believe that it might be true, because in other studies [24, 50], changes in OCT were observed in advanced but not in the early stages of AD.

The dysfunction of retinal ganglion cells and the optic nerve may, at least partially, explain the cause of visual disturbances reported by patients with the early stages of Alzheimer’s disease and with apparently normal eyes.

This dysfunction might be a characteristic feature of AD and may be useful in the differential diagnosis. Further investigations in a larger group of patients with AD and also in patients with other types of dementia are necessary to confirm our suggestion.