Subtle changes in the retina, optic nerve and visual processing system may reveal early signs of Alzheimer’s disease and enable prompt initiation of treatment.
Reviewed by Dr Robert C. Sergott.
Signs and symptoms of Alzheimer’s disease in the retina, optic nerve and the more posterior afferent visual system in the temporal and parietal lobes may point physicians to a diagnosis of Alzheimer’s disease earlier than previously realised, according to Dr Robert C. Sergott, director of the Neuro-Ophthalmology Service at Wills Eye Hospital and founding director and CEO of the Annesley EyeBrain Center at Thomas Jefferson University in Philadelphia, Pennsylvania, United States.
Dr Sergott pointed out the importance of being aware of the—often—subtle signs and symptoms in patients 55 years and older. With diseases such as Alzheimer’s disease and Parkinson’s disease, patients may present first to an ophthalmologist rather than a neurologist because of the associated visual disturbances.
Dr Sergott described a 68-year-old man who presented with progressive field constriction for 2 years and the inability to drive at night for approximately 1½ years. The patient described seeing oncoming lights when driving as starbursts.
Constricted visual fields may be an initial presentation of possible Alzheimer’s disease. However, the differential diagnosis is large and includes retinal degenerations; quinine toxicity; central retinal artery occlusion; end-stage glaucoma or papilloedema; confluent optic disc drusen; bilateral occipital lobe infarctions; non-physiological response; and cognitive impairment on automated perimetry.
Dr Sergott explained that visual field constriction implicates a visual field defect in the retina, optic nerve or occipital lobe; the photophobia, a problem in the retina; and night blindness and depth perception, a retinal or cortical issue. Consideration of the three locations suggests that there may be more of a retinal or a cortical problem, or both.
“Alzheimer disease affects them all: i.e., the retina, optic nerve and the visual system posterior to the lateral geniculate,” he said. The patient’s history was positive for prostate cancer and basal and squamous cell cancers, without metastases; hypertension; and hyperlipidaemia.
“A rule to live by in neuro-ophthalmology is to determine if the patient’s problem at hand is caused by the cancer recurrence, especially with breast cancer, or cancer therapy,” Dr Sergott emphasised. The patient’s ocular examination was unremarkable, with 20/40 vision bilaterally.
Interestingly, the patient could see only the test Ishihara plate, although he had no history of colour blindness. The acquired loss of colour vision could be in the cones, optic nerve or cortical system.
“This provides a subtle hint of an afferent visual problem. Colour vision measures contrast sensitivity,” Dr Sergott said. “Using low-contrast visual acuity [VA], a deficit worse than 20/40 might be identified.”
Optical coherence tomography imaging was unremarkable but showed slight flattening, with the fovea-macular contour slightly broadened. Fundus autofluorescence also showed no striking abnormality suggestive of early Alzheimer’s disease.
Multifocal electroretinography (ERG), however, showed an almost isoelectric tracing in the right eye despite 20/40 vision. In the left eye, multifocal ERG abnormalities were present but was not as pronounced as in the right eye.
Cranial MRI showed both non-specific changes and that paraneoplastic autoantibodies and the lumbar puncture cerebrospinal fluid profile were negative. Automated perimetry showed an inferior quadrantanopia in the left eye and a more subtle defect in the right eye. This localisation pattern was in the right parietal temporal lobe.
“From this testing, we know that this patient has brain disease in the right parietal temporal lobe,” Dr Sergott explained. “The multifocal ERG results indicated the presence of retinal disease. This proved to be an extensive process in the visual system.”
In addition to the constricted visual fields, colour vision deficit and abnormal ERG, the patient’s history showed dissatisfaction with the results of cataract surgery despite 20/40 bilateral VA and a depth perception of only 40 seconds of arc. “One reason for dissatisfaction postoperatively with a good Snellen VA may be Alzheimer’s disease,” he said.
“The root of the dissatisfaction may be subtle problems with difficulty reading and finding words and mild short-term memory loss.” Other clues are that the patient never arrived alone at appointments and often did not answer questions directed to them, Dr Sergott added.
Patients who present with predominantly visual symptoms may have posterior cortical atrophy.
However, Dr Sergott cautioned physicians about recognising patients who present with mildly disrupted memory and functioning, which may point to other findings suggestive of a more global deficit of visual processing. These may include a progressive decline in visuospatial, visual perception and literacy skills appearing in patients who are on average 50 to 65 years of age.
Experts disagree about whether posterior cortical atrophy is a pure form of Alzheimer’s disease or a separate entity. Lewy body dementia and prion disease may also have similar visual symptoms.
Dr Sergott summarised the various ophthalmological findings that ophthalmologists should prioritise when confronted with similar patients to the one described. The presentations of Alzheimer’s disease include the unhappy patient with good VA after cataract surgery and, in patients who have not had recent cataract surgery, loss of colour vision, loss of depth perception and photoreceptor dysfunction manifesting as glare and night blindness.
Dr Sergott also advised physicians to be alert to patients with visual field defects who have trouble with the automated perimetry test, especially with repeated attempts. Patients may also present with a homonymous hemianopsia but a normal MRI scan. This clinical presentation should alert ophthalmologists and neurologists to the possibility of Alzheimer’s disease.
“When such patients present, Alzheimer’s disease should be suspected. Hopefully, during 2021 some treatments will become available,” Dr Sergott said. “[As with] most treatments, they will work better the sooner they are instituted before the disease destroys most of the brain and a large segment of the retinal and optic nerve function. Ophthalmologists may be the key to get the diagnostic process moving.”
Dr Sergott added that he believes that the multifocal ERG may be the most sensitive test to identify retinal abnormalities in patients with dementia syndromes.
Robert C. Sergott, MD
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