Research Article - Biomedical Research (2017) Volume 28, Issue 13
Relationships between optic nerve damage and the severity of cognitive impairment in patients with mild cognitive impairment and Alzheimer's disease
Lina Zhang1,2, Yuming Xu3 and Yu Zhu1*1Department of Ophthalmology, the First Affiliated Hospital of Zhengzhou University, PR China
2Department of Ophthalmology, People's Hospital of Zhengzhou, PR China
3Department of Neurology, the First Affiliated Hospital of Zhengzhou University, PR China
- *Corresponding Author:
- Yu Zhu
Department of Ophthalmology
The First Affiliated Hospital of Zhengzhou University, PR China
Accepted on May 9, 2017
Abstract
This study was to analyse the degeneration of the Retinal Nerve Fiber Layer (RNFL) and optic disc and the relationship between optic nerve damage and the severity of cognitive impairment in patients with Alzheimer’s disease (AD) and Mild Cognitive Impairment (MCI). The RNFL thickness and optic disc variables were assessed by optical coherence tomography in patients with MCI and AD and control subjects. Moreover, the correlation coefficients among RNFL thickness, optic disc parameters, and Mini- Mental State Examination (MMSE) scores were investigated in AD and MCI patients. RNFL thickness was significantly thicker in control group than that in the other two groups (P<0.05). The significant difference was detected between groups AD and MCI (P<0.05). Cup-to-disc ratio and pallor area-to-disc area ratio were increased but disc rim area was reduced in groups MCI and AD compared with in normal group (P<0.05). The significant difference was existed between groups AD and MCI (P<0.05). Pearson’s correlation test showed that compared with MMSE scores there was negative correlations in cup-to-disc ratio (P<0.05) and pallor-to-disc area ratio (P<0.01), but positive correlations in total RNFL thickness (P<0.01) and disc rim area (P<0.01). These results indicated that there was the degeneration of RNFL in MCI and AD patients. Moreover, the correlations among RNFL thickness, optic disc parameters and MMSE scores revealed that the severity of the optic nerve damage was increased along with the aggravation of the disease.
Keywords
Retinal nerve fiber layer, Optic disc, Alzheimer’s disease, Mild cognitive impairment, Optical coherence tomography.
Introduction
As people grow older, the incidence of Alzheimer’s disease (AD) increases gradually. By some estimates more than 100 million persons will suffer from AD by 2050 [1]. As everyone knows, patients with AD have visual problems including reduced visual acuity, visual field defects, impaired color discrimination, changes in smooth and saccadic eye movements, alterations in visual evoked potentials and fixation defects [2,3]. Mild Cognitive Impairment (MCI) is a broad term that encompasses several subtypes, among which amnestic MCI may be an early transitional stage to AD [4]. MCI is more likely to progress to AD by 10% per year, compared with 1% of normal subjects [5,6]. Due to the increasing incidence of AD and MCI more researches are needed to prevent AD as well as the related retinal changes. Thus, many ways have been tried to investigate the Retinal Nerve Fiber Layer (RNFL) thickness and optic disc in AD and MCI.
Optical Coherence Tomography (OCT) is a new non-invasive examination that can assess the RNFL thickness and optic disc variables, and is used in various ophthalmologic diseases including ocular hypertension, glaucoma, Alzheimer’s disease, Parkinson’s disease and multiple sclerosis [7]. RNFL is thin in Alzheimer’s disease and multiple sclerosis, which may be a structural biomarker for the damage of the optic nerve [8]. Some reports have described the degeneration of the RNFL and optic disc in AD [9-12]. Hinton et al. [9] first reported the study of retinal damage which showed widespread damage in the optic nerve with reduced RNFL thickness. Berisha et al. [10] hypothesized that a specific superior RNFL loss could be detected by OCT in patients with early AD. Tsai et al. [11] found that cup-to-disc ratio, optic disc volume and disc rim area in patients with AD were significantly changed compared with normal group. However, there still were contradictory standpoints about RNFL and optic disc changes in AD or MCI. For example, Kergoat et al. [13] found no difference in RNFL thickness was observed between AD and healthy subjects. All in all, these findings indicated that different methodologies may be responsible for the results discrepancy. In addition, the data about optic disc (cup-to-disc ratio, pallor area-to-disc area and disc rim area) were scarce.
The aim of the present study was to assess whether the RNFL and optic disc were degenerate definitely and whether there was a relationship between optic nerve damage and the severity of cognitive impairment in patients with AD and MCI.
Materials and Methods
Subjects
Forty nine MCI patients and forty six AD patients were obtained from department of neurology; forty nine agematched controls were obtained from department of ophthalmology in the First Affiliated Hospital of Zhengzhou University in 2014 and 2015. All patients signed informed consent. The study adhered to the guidelines of the Declaration of Helsinki, and was approved by ethic committee of the First Affiliated Hospital of Zhengzhou University, China.
The AD patients were diagnosed by neurologists in the First Affiliated Hospital of Zhengzhou University and met criteria for AD set by the National Institute of Neurologic and Communicative Disorders and Stroke-Alzheimer’s Disease and Related Disorders Association (NINCDS-ADRDA) guidelines and the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) criteria [14,15]. We used Petersen criteria for the diagnosis of MCI [16]. Each patient with AD or MCI underwent a detailed neurological examination including laboratory and neuro-imaging evaluations, and psychometric test. Cognitive function was evaluated by means of the Mini- Mental State Examination (MMSE) [17] in AD, MCI and control groups. The criteria for normal control were: (1) no dementia or cognitive impairment; (2) MMSE scores above 28. The criteria for MCI were: (1) memory complaints; (2) MMSE scores above 25; (3) abnormal behaviors at the MMSE (missing two or three words).
Some patients were excluded due to some certain conditions that are capable of affecting RNFL thickness, such as glaucoma, increased intraocular pressure, optic neuropathy, diabetic retinopathy, macular degeneration, retinal artery occlusion, cerebral infarction, Parkinson’s disease, cerebral apoplexy and other diseases.
Method
All subjects underwent ophthalmological examination including visual acuity, diopter, slit lamp biomicroscopy, Intraocular Pressure (IOP), direct ophthalmoscopy, indirect ophthalmoscopy and optical coherence tomography. The examinations were performed by an experienced technician with blinded method. The IOP was measured by Goldmann applanation tonometer. By OCT total RNFL thickness and optic disc parameters were measured in both eyes of every subject and only one eye for high quality image was selected into the study (Stratus 3000, Carl Zeiss). The RNFL thickness scan mode with a diameter of 3.4 mm centered on the optic disc was used and the software automatically calculated the RNFL thicknesses. The optic disc scan was got from six linear scans centered on the optic disc and the software automatically measured the optic disc parameters. Every eye was repeatedly scanned for three times and the average value was considered to be the reliable data.
Statistical analysis
SPSS 16.0 data analysis software (SPSS Inc., USA) was used. All clinical data were expressed as mean ± Standard Deviation (SD). The chi-square test was used to compare the difference in sex among three groups. One way Analysis of Variance (ANOVA) was used to compare the differences in age, IOP, RNFL thickness and optic disc parameters among three groups following post hoc comparison between groups by Bonferroni correction. Spearman's correlation coefficient analysis was applied to analyse the correlations among the retinal nerve fiber layer thickness, optic disc variables and MMSE scores. P value less than 0.05 was statistically significant.
Results
There were 49 patients participated in our research. The descriptive data in MCI, AD and control groups were summarized in Table 1. No significant differences in sex, age, or IOP were found among three groups (P>0.05). The results indicated that sex, age and IOP had no effect on the comparison of RNFL thickness and optic disc.
Control (n=49) | MCI (n=49) | AD (n=46) | P value | |||
---|---|---|---|---|---|---|
Sex | M | 24 | 22 | 24 | χ2=0.451 | |
F | 25 | 27 | 22 | |||
Age (y) | 71.1 ± 8.6 | 70.9 ± 6.1 | 72.8 ± 5.2 | F=2.121 | >0.05 | |
IOP (mmHg) | 15.1 ± 6.5 | 17.1 ± 7.6 | 16.1 ± 5.2 | F=2.759 | >0.05 |
MCI: Mild Cognitive Impairment; AD: Alzheimer’s Disease; n: Eyes; M: Male; F: Female; IOP: Intraocular Pressure.
Table 1. The descriptive data of patients with MCI, AD and control groups (mean ± SD).
Total RNFL thickness and optic disc variables values in patients with MCI, AD and control subjects were illustrated in Table 2. The results showed (1) RNFL thickness: RNFL thickness was significantly thicker in the control group compared to the other two groups (P<0.05), the significant difference was detected between groups AD and MCI (P<0.05); (2) optic disc variables: cup-to-disc ratio and pallor area-to-disc area ratio were increased but disc rim area was reduced in groups MCI and AD compared with the normal group (P<0.05), the significant difference was existed between groups AD and MCI (P<0.05). These data suggested the thinner RNFL consistent with higher cup-to-disc ratio and pallor area-to-disc area ratios and lower disc rim area proved the damage of optic nerve in MCI and AD patients.
Control | MCI | AD | F value | |
---|---|---|---|---|
T | 100.12 ± 15.01 | 92.52 ± 19.23▲ | 87.13 ± 17.05▲■ | 7.985** |
C/D | 0.42 ± 0.61 | 0.48 ± 0.65▲ | 0.53 ± 0.22▲■ | 5.115** |
P/D | 0.26 ± 0.11 | 0.35 ± 0.26▲ | 0.319 ± 0.32▲■ | 6.121** |
D | 2.01 ± 0.61 | 1.83 ± 0.29▲ | 1.51 ± 0.32▲■ | 8.923** |
MCI: Mild Cognitive Impairment; AD: Alzheimer’s Disease; T: Total (µm); C/D: Cup-to-Disc ratio; P/D: Pallor-to-Disc area ratio; D: Disc Rim Area (mm3); Comparison to the control group: ▲P<0.05; comparison to MCI: ■P<0.05; ANOVA: *P<0.05, **P<0.01.
Table 2. Total RNFL thickness and optic disc variables values in patients with MCI, AD and control subjects (mean ± SD).
From the Table 3, the correlation coefficient among RNFL thickness, cup-to-disc ratio, pallor-to-disc area ratio, disc rim area and MMSE scores were revealed. Pearson’s correlation test showed that compared with MMSE scores there was negative correlations in cup-to-disc ratio (P<0.05) and pallorto- disc area ratio (P<0.01), but positive correlations in total RNFL thickness (P<0.01) and disc rim area (P<0.01). The correlation coefficient among RNFL thickness, optic disc parameters and MMSE scores revealed that the severity of the optic nerve degeneration increased along with the aggravation of the disease.
MMSE | |
---|---|
Total RNFL thickness (µm) | 0.256** |
cup-to-disc ratio | -0.192* |
pallor-to-disc area ratio | -0.251** |
disc rim area (mm3) | 0.216** |
MMSE: mini-mental state examination; Spearman's correlation analysis: *P<0.05, **P<0.01.
Table 3. Correlation coefficient among RNFL thickness, cup-to-disc ratio, pallor-to-disc area ratio, disc rim area and MMSE.
Discussion
Retinal nerve fiber layer thickness and optic disc
According to above results, several aspects would be addressed. The first question involves the changes of RNFL thickness and optic disc. RNFL thickness is thin in Alzheimer’s disease and multiple sclerosis, which may be a structural biomarker for the damage of the optic nerve [8]. RNFL thickness by OCT in previous investigation showed that significantly thin RNFL was found in patients with AD compared with control subjects [10]. Paquet et al. [18] compared RNFL thickness by OCT among healthy control subjects, MCI, mild AD, and moderate-to-advanced AD. All three groups showed significant difference compared with the healthy control group. No significant difference was found between mild AD and MCI [18]. Other studies by Parisiet [19] and Iseri et al. [20] also indicated there was an obvious reduction of RNFL thickness for AD and MCI patients. In line with the findings, we also found significant difference with respect to RNFL thickness among AD, MCI, and healthy control groups, especially between AD and MCI.
There are more studies concerning RNFL thickness in AD with the OCT technique. However, there are only a few data that have assessed the optic disc variables. In this study, we investigated optic disc parameters by OCT among three groups. The research found that the patients with MCI and AD showed obviously changes in cup-to-disc ratio, pallor-to-disc area ratio and disc rim area. Consistent with our findings, in 1991, Tsai et al. [11] found that cup-to-disc ratio, optic disc volume and disc rim area were significantly changed and were related to MMSE and durations of disease with the use of retinal nerve fiber photography and computerized image analysis of the optic nerve head. Lu et al. [21] showed that the cup-disc ratio in AD patients was increased by 39-43% when compared to that in the control group. A case control study also showed that an obvious defection in AD patients’ RNFL was found and that there was a 3-fold greater odds ratio demonstrating the increased cupping in AD [22]. The results of our study proved the optic nerve damage existed in AD and MCI.
To our knowledge, RNFL is a region that is sensitive to axonal and neuronal loss as it contains ganglionic cell neurons originating from optic nerve and their axons [23]. Retinal nerve fibers converge together when they exit from the eye and descend through the lamina cribrosa becoming the optic disc. Retinal nerve fiber layer is association with optic disc closely. Therefore, the thin RNFL is consistent with large cup-to-disc ratio and pallor area-to-disc area ratios and small disc rim area. By OCT the changes in retina and optic disc had been identified in patients with AD, including significant decrease in RNFL thickness and disc rim area and increase in cup-to-disc ratio and pallor-to-disc area ratio. In addition, some scholars have speculated that the disc rim area more exactly and directly reflect the severity of optic nerve damage than the cup-to-disc ratio and pallor-to-disc area ratio [24]. The loss of disc rim area was typically morphological change of optic nerve degeneration, and it was less affected by age, refraction and optic disc size [24]. Thus, it is obvious that RNFL and optic disc, especially disc rim area, could be used as sensitive indicators of optic nerve damage in patients with AD and MCI by OCT.
Many previous reports indicated that the damage in retina and optic disc were attributed to nerve degeneration only in primary visual cortex [25-27]. Armstrong [28] found axons from retina project to primary visual cortex, senile plaques and neurofibrillary tangles in primary visual cortex may cause the damage in retina and optic nerve. Other studies revealed that patients with AD had senile plaques and neurofibrillary tangles in primary visual pathways (optic nerve and retina), leading to the damage of retina [29]. Tsai et al. [11] suggested that the degeneration of retinal nerve fiber layer and optic disc might possibly ascribe to both antegrade degeneration secondary to retinal ganglion cell degeneration and retrograde degeneration originating at optic tract or visual cortex. The question need to be clarified is the relationship (succession or parallel) between visual cortex and primary visual pathways.
The relationship between optic nerve damage and the severity of cognitive impairment
Many studies have showed that RNFL thickness is measured by OCT in AD patients. However, the number of studies about the relationship between optic nerve damage and the severity of cognitive impairment is still limited [19,30,31]. In this study, we investigated the relationships among RNFL thickness, optic disc and MMSE scores. In 1991, Tsai et al. [11] found that cup-to-disc ratio, optic disc volume and disc rim area were significantly changed and were related to MMSE and durations of disease. Although pallor area-to-disc area ratio was not significantly different, the patients with higher pallor area-to-disc area ratios had a higher MMSE scores and longer durations of disease with the use of retinal nerve fiber photography and computerized image analysis of the optic nerve head between patients with AD and controls. Paquet et al. [18] found no significant relationship between MMSE scores and RNFL measurement by OCT among healthy control subjects, MCI, mild AD, and moderate-to-advanced AD [18]. Our results also showed that the RNFL thickness was thinner, disc rim area was decreased and cup-to-disc ratio and pallor area-to-disc area ratios were larger from MCI to AD. Like the existing data, our study revealed the severity of the optic nerve degeneration increased along with the aggravation of the cognitive impairment. The relationship played an important role for RNFL and optic disc analysis by OCT in monitoring the development of AD and in assessing the effect of treatment.
In contrast to these studies, no significant difference was reported between RNFL and MMSE scores. For example, a study proved that the damage in visual function occurring in dementia of the Alzheimer’s type were not related to optic nerve head structural anomalies, at least in the earlier stage of AD [13]. Kergoat et al. [13] found no difference was observed between AD and control subjects in RNFL thickness by scanning laser polarimetry. The reason for difference may include a low sample size and methodological difference.
MCI
MCI is a risk factor for AD. Extensive research is being devoted to prevent MCI converting to AD. The damage of RNFL thickness and optic disc in MCI indicates that the change of retina and optic nerve is an early event in the development of this disease. OCT is a safe and reproducible method to assess retina and optic nerve degeneration in AD and MCI. By OCT we were able to early detect MCI and prevent MCI progress to AD.
Our study also had some limitations. First, the limitation of the study is the relatively small sample size because of the strict inclusion criteria. The study mainly included patients with mild-to-moderate Alzheimer disease due to poor coordination of severe Alzheimer’ disease patients and this may affect the accuracy of the results. A follow-up study is needed to further prove the relationship between optic nerve damage and the severity of disease progression. Therefore, a larger cohort of MCI and AD patients and a follow-up study are needed to confirm these conclusions.
Conclusion
Acknowledgements
First of all, I express my deepest appreciation to Prof. Yu Zhu for assistance with the experiments and valuable discussion. Second, I thanks for Dr. Yuming Xu providing language and writing help. Third, I am very grateful to my colleagues for doing examination for our study subjects.
Conflicts of Interest
The authors declare that they have no financial or other conflicts of interest in relation to this research and its publication.
References
- Brookmeyer R, Johnson E, Ziegler-Graham K, Arrighi HM. Forecasting the global burden of Alzheimers disease. Alzheimers Dement 2007; 3: 186-191.
- Armstrong RA. Alzheimers disease and the eye. J Optom 2009; 2: 103-111.
- Valenti DA. Alzheimers disease: visual system review. Optometry 2010; 81: 12-21.
- Petersen RC, Doody R, Kurz A, Mohs RC, Morris JC. Current concepts in mild cognitive impairment. Arch Neurol 2001; 58: 1985-1992.
- Petersen RC. Mild cognitive impairment as a diagnostic entity. J Intern Med 2004; 256: 183-194.
- Petersen RC, Stevens JC, Ganguli M, Tangalos EG, Cummings JL, DeKosky ST. Practice parameter: early detection of dementia: Mild cognitive impairment (an evidence-based review). Report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology 2001; 56: 1133-1142.
- Jaffe GJ, Caprioli J. Optical coherence tomography to detect and manage retinal disease and glaucoma. Am J Ophthalmol 2004; 137: 156-169.
- Fisher JB, Jacobs DA, Markowitz CE, Galetta SL, Volpe NJ, Nano-Schiavi ML, Baier ML, Frohman EM, Winslow H, Frohman TC, Calabresi PA, Maguire MG, Cutter GR, Balcer LJ. Relation of visual function to retinal nerve fiber layer thickness in multiple sclerosis. Ophthalmology 2006; 113: 324-332.
- Hinton DR, Sadun AA, Blanks JC, Miller CA. Optic-nerve degeneration in Alzheimers disease. N Engl J Med 1986; 315: 485-487.
- Berisha F, Feke GT, Trempe CL, McMeel JW, Schepens CL. Retinal abnormalities in early Alzheimers disease. Invest Ophthalmol Vis Sci 2007; 48: 2285-2289.
- Tsai CS, Ritch R, Schwartz B, Lee SS, Miller NR. Optic nerve head and nerve fiber layer in Alzheimers disease. Arch Ophthalmol 1991; 109: 199-204.
- Sadun AA, Bassi CJ. Optic nerve damage in Alzheimers disease. Ophthalmology 1990; 97: 9-17.
- Kergoat H, Kergoat MJ, Justino L, Chertkow H, Robillard A, Bergman H. An evaluation of the retinal nerve fiber layer thickness by scanning laser polarimetry in individuals with dementia of the Alzheimer type. Acta Ophthalmol Scand 2001; 79: 187-191.
- McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM. Clinical diagnosis of Alzheimers disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimers disease. Neurology 1984; 34: 939-944.
- Diagnostic and Statistical Manual of Mental Disorders (DSM-IV). Washington DC: American Psychiatric Association (4th Edn.) 1994.
- Petersen RC. Mild cognitive impairment: current research and clinical implications. Semin Neurol 2007; 27: 22-31.
- Lobo A, Saz P, Marcos G, Dia JL, de la Camara C, Ventura T, Morales Asin F, Fernando Pascual L, Montanes JA, Aznar S. Revalidation and standardization of the cognition mini-exam (first Spanish version of the Mini-Mental Status Examination) in the general geriatric population. Med Clin (Barc) 1999; 112: 767-774.
- Paquet C, Boissonnot M, Roger F, Dighiero P, Gil R. Abnormal retinal thickness in patients with mild cognitive impairment and Alzheimers disease. Neurosci Lett 2007; 420: 97-99.
- Parisi V, Restuccia R, Fattapposta F, Mina C, Bucci MG. Morphological and functional retinal impairment in Alzheimers disease patients. Clin Neurophysiol 2001; 112: 1860-1867.
- Iseri PK, Altinas O, Tokay T, Yüksel N. Relationship between cognitive impairment and retinal morphological and visual functional abnormalities in Alzheimer disease. J Neuroophthalmol 2006; 26: 18-24.
- Lu Y, Li Z, Zhang X, Ming B, Jia J, Wang R, Ma D. Retinal nerve fiber layer structure abnormalities in early Alzheimers disease: evidence in optical coherence tomography. Neurosci Lett 2010; 480: 69-72.
- Danesh-Meyer HV, Birch H, Ku JY, Carroll S, Gamble G. Reduction of optic nerve fibers in patients with Alzheimer disease identified by laser imaging. Neurology 2006; 67: 1852-1854.
- Oktem EO, Derle E, Kibaroglu S, Oktem C, Akkoyun I, Can U. The relationship between the severity of cognitive impairment and retinal nerve fiber layer thickness. Neurol Sci 2015; 36: 1141-1146.
- Henson DB, Artes PH, Chauhan BC. Diffuse loss of sensitivity in early glaucoma. Invest Ophthalmol Vis Sci 1999; 40: 3147-3151.
- Cogan DG. Visual disturbances with focal progressive dementing disease. Am J Ophthalmol 1985; 100: 68-72.
- Nissen MJ, Corkin S, Buonanno FS, Growdon JH, Wray SH. Spatial vision in Alzheimers disease. General findings and a case report. Arch Neurol 1985; 42: 667-671.
- Schlotterer G, Moscovitch M, Crapper-McLachlan D. Visual processing deficits as assessed by spatial frequency contrast sensitivity and backward masking in normal ageing and Alzheimers disease. Brain 1984; 107: 309-325.
- Armstrong RA. Visual field defects in Alzheimers disease patients may reflect differential pathology in the primary visual cortex. Optom Vis Sci 1996; 73: 677-682.
- Ho WL, Leung Y, Tsang AW, So KF, Chiu K, Chang RC. Review: Tauopathy in the retina and optic nerve: does it shadow pathological changes in the brain? Mol Vis 2012; 18: 2700-2710.
- Bowd C, Zangwill LM, Blumenthal EZ, Vasile C, Boehm AG, Gokhale PA, Mohammadi K, Amini P, Sankary TM, Weinreb RN. Imaging of the optic disc and retinal nerve fiber layer: the effects of age, optic disc area, refractive error, and gender. J Opt Soc Am A Opt Image Sci Vis 2002; 19: 197-207.
- Kesler A, Vakhapova V, Korczyn AD, Naftaliev E, Neudorfer M. Retinal thickness in patients with mild cognitive impairment and Alzheimers disease. Clin Neurol Neurosurg 2011; 113: 523-526.