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 Table of Contents  
CORRESPONDENCE
Year : 2018  |  Volume : 131  |  Issue : 19  |  Page : 2357-2359

Systemic-Related Factors of Nonarteritic Anterior Ischemic Optic Neuropathy


1 Beijing Tongren Eye Center, Beijing Key Laboratory of Intraocular Tumor Diagnosis and Treatment, Beijing Ophthalmology and Visual Sciences Key Laboratory, Beijing Tongren Hospital, Capital Medical University, Beijing 100730; Department of Ophthalmology, Beijing Airport Hospital, Beijing 101318, China
2 Beijing Tongren Eye Center, Beijing Key Laboratory of Intraocular Tumor Diagnosis and Treatment, Beijing Ophthalmology and Visual Sciences Key Laboratory, Beijing Tongren Hospital, Capital Medical University, Beijing 100730, China
3 Department of Ophthalmology, Kailuan General Hospital, Tangshan, Hebei 063000, China
4 Department of Cardiology, Kailuan General Hospital, Tangshan, Hebei 063000, China
5 Department of Respiratory, Kailuan General Hospital, Tangshan, Hebei 063000, China

Date of Submission20-Jun-2018
Date of Web Publication21-Sep-2018

Correspondence Address:
Prof. Wen-Bin Wei
Beijing Tongren Eye Center, Beijing Key Laboratory of Intraocular Tumor Diagnosis and Treatment, Beijing Ophthalmology and Visual Sciences Key Laboratory, Beijing Tongren Hospital, Capital Medical University, Beijing 100730
China
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0366-6999.241795

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How to cite this article:
Xiao YY, Wei WB, Wang YX, Lu AD, Chen SH, Song L, Wu SL. Systemic-Related Factors of Nonarteritic Anterior Ischemic Optic Neuropathy. Chin Med J 2018;131:2357-9

How to cite this URL:
Xiao YY, Wei WB, Wang YX, Lu AD, Chen SH, Song L, Wu SL. Systemic-Related Factors of Nonarteritic Anterior Ischemic Optic Neuropathy. Chin Med J [serial online] 2018 [cited 2018 Oct 19];131:2357-9. Available from: http://www.cmj.org/text.asp?2018/131/19/2357/241795



To the Editor: Nonarteritic anterior ischemic optic neuropathy (NAION) is an acute optic neuropathy disease that is common in the elderly. The incidence of NAION is approximately (2.3–10.2)/100,000, and both eyes are involved in many patients. Xu et al.[1] reported that the incidence in the Chinese population was 1/16,000. Acute visual acuity (VA) damage without any pain and a poor prognosis are the main features of NAION. This study aimed to find the related risk factors for NAION in average individuals to promote the prevention or early diagnosis of NAION.

This study was approved by the Ethics Committees of Kailuan General Hospital, China. The data are anonymous, and the requirement for informed consent was therefore waived.

The study was a retrospective study based on the Kailuan study and the Kailuan medical database. The Kailuan study is an ongoing longitudinal cohort study that began in 2006 and is based on the Kailuan community.[2] The Kailuan study includes employees and retirees of the Kailuan Group Company. All participants underwent questionnaire assessments and clinical and laboratory examinations, which were conducted in the 11 hospitals responsible for the health care of this community, residing in Tangshan city. The information collected had been reported before.[2] The study was performed according to the guidelines of the Helsinki Declaration and was approved by the Ethics Committee of the Kailuan General Hospital. All participants signed a written informed consent form.

The diagnosis of NAION was searched in the Kailuan medical database of the Kailuan Corporation between 2006 and 2015 and was confirmed by detailed records in the hospital where the disease was diagnosed. All the other people in the 2006 Kailuan study database composed the control group. The medical records of the patients, excluding those patients without detailed medical records or with an unclear diagnosis, were checked. The demographic data, including age, gender, lifestyle, dietary habits, complicated systemic diseases, and drug usage of the patients, were recorded. The ophthalmic evaluation results, including VA, intraocular pressure, slit-lamp examination of the anterior segment, lens, and vitreous, stereoscopic color fundus photography, fluorescein fundus angiography, and visual field (VF) with automated perimeter, were also recorded. Furthermore, the results of carotid ultrasound, echocardiography, cranial computed tomography scan, and blood tests were recorded. Body mass index (BMI) = body weight/height2 (kg/m2). The estimated glomerular filtration rate was calculated with the Chronic Kidney Disease-Epidemiology Collaboration equation. Other systemic or neurologic investigations were also performed to rule out any related causes of visual loss.

The inclusion criteria were as follows: (1) a history of sudden visual loss, without other ocular, systemic, or neurological diseases that might cause visual damage; (2) optic disc edema; and (3) optic disc-related VF defects.

Exclusion criteria were as follows: (1) other diseases that can cause edema of the optic disc, such as a brain tumor; (2) other ocular diseases that can cause VF defects, such as retinal detachment, vitreous hemorrhage, and glaucoma; (3) complications from systemic autoimmune diseases; (4) any evidence suggestive of temporal arteritis, such as a history of scalp tenderness, Westergren sedimentation rate ≥40 mm/h, or positive C-reactive protein; and (5) those without a detailed medical record.

A retrospective cohort analysis method was used for this study. First, the measurement data and enumeration data were statistically analyzed with the t-test and Chi-square test, respectively. Then, single variable logistic regression was used to analyze the related risk factors. Gender, age, and factors with a significant difference in the single variable logistic regression analysis were included in the multivariate logistic regression analysis. SPSS 13.0 software (SPSS Inc., Chicago, IL, USA) was used for the statistical analysis. P < 0.05 was considered statistically significant.

There were 85 patients in the database with a diagnosis of NAION. A total of 38 patients were included as the case group to make an analysis according to the criteria. There were 101,510 patients in the Kailuan study group in 2006. Therefore, the other 101,472 patients served as the control group. The mean age of the NAION group was 54.55 ± 8.19 years. The mean age of the control group was 51.93 ± 12.67 years. Age and gender were not significantly different between the two groups.

There were 18 patients (47.4%) with a VA better than 0.3. A total of 12 patients (31.6%) had a VA between 0.1 and 0.3. A total of eight patients (21.1%) had a VA below 0.1. A total of two patients (5.3%) had a two-line VA or better after taking medicine to improve microcirculation. In addition, six patients (15.8%) had a worse VA after taking the medicine. The other 30 patients (78.9%) had no change in VA. The automated perimeter was used to test the VF in 30 patients (78.9%). VF defects were present in all of these patients, three cases of whom had inferior altitudinal defects, seven cases of whom had superior arcuate scotoma defects, five cases of whom had nasal periphery defects, four cases of whom had temporal periphery defects, and two cases of whom had tubular VF defects. The other nine patients had irregular VF defects.

A total of 30 patients (78.9%) in the NAION group underwent cranial CT scan, and nine of these patients (30.0%) had infarction. The lesion location was either single or multiple. The basal ganglia were involved in five patients (55.6%). The centrum semiovale was involved in four patients (44.4%). The brainstem, parietal lobe, and lateral ventricles were also occasionally involved.

The most common systemic comorbidity in the NAION group was hyperlipidemia (19 patients, 50%), which was followed by hypertension (12 patients, 31.6%), stroke (nine patients, 23.7%), diabetes mellitus (seven patients, 18.4%), and coronary heart disease (five patients, 13.2%). In the control group, hyperlipidemia was also the most common comorbidity (69,868 patients, 68.8%), which was followed by hypertension (44,212 patients, 43.6%) and diabetes mellitus (9,482 patients, 9.3%).

The basic overall information analysis showed that waist circumference, hip circumference, abdominal circumference, BMI, physical exercise, drinking, fasting plasma glucose (FPG), hyperlipidemia, and stroke history showed significant differences between the two groups [Table 1]. Single variable logistic regression analysis showed that BMI (P = 0.023, odds ratio [OR] = 1.113, 95% confidence interval [CI]: 1.015–1.220), FPG (P < 0.001, OR = 1.221, 95% CI: 1.105–1.349), hyperlipidemia (P = 0.015, OR = 0.453, 95% CI: 0.240–0.855), and stroke history (P < 0.001, OR = 12.012, 95% CI: 5.680–25.400) showed significant differences between the two groups. Multivariate logistic regression analysis showed that BMI (P = 0.042, OR = 1.109, 95% CI: 1.004–1.225), FPG (P < 0.001, OR = 1.218, 95% CI: 1.093–1.357), and stroke history (P < 0.001, OR = 9.291, 95% CI: 3.185–27.107) were the independent risk factors for NAION. The other factors showed no significant differences between the two groups.
Table 1: Overall information analysis

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NAION is an optical neural lesion accompanied by acute microcirculatory disturbances. Many risk factors for NAION have been reported, such as old age, crowded optic discs, hypertension, hyperlipidemia, diabetes mellitus, hypercoagulability, and protein S.

Kosanovic-Jakovic et al.,[3] in the research on the relationship between metabolic syndrome and NAION, reported that obesity was related to NAION. Multivariate Logistic regression analysis showed that BMI was an independent risk factor for NAION. This result means that controlling BMI or obesity can protect patients from NAION.

Many diabetic patients are in a hypercoagulability state, which is accompanied by dysfunction of the microcirculation, inducing susceptibility to NAION.[4] The results of this study showed that diabetes mellitus itself was not an independent risk factor for NAION but that FPG (P < 0.001, OR = 1.218, 95% CI: 1.093–1.357) is an independent risk factor for NAION. The actual mechanism of pathogenesis of this disease is unclear, but this result may help to identify it.

The main branches of the internal carotid artery system in the brain are the ophthalmic artery, the anterior cerebral artery, the middle cerebral artery, the anterior choroidal artery, and the posterior communicating artery. The basal ganglia are supplied by the deep perforating branch of the middle cerebral artery. Dysfunction in blood circulation in the anterior region of the lamina cribrosa may lead to NAION. Stroke was a common comorbidity in NAION patients, and it mainly involved the basal ganglia region. The results of this study showed that stroke history was an independent risk factor for NAION (P < 0.001, OR = 9.291, 95% CI: 3.185–27.107). Some researchers reported that the risk for NAION was greater for those with stroke history.[5] The shared vascular origin of these two diseases may be the cause of this outcome.

In this study, the risk factors for NAION were analyzed in a large population, which may lead to a conclusion consistent with the real trend. Controlling BMI and FPG can help prevent NAION. To make an earlier diagnosis and therapy decision in stroke patients, these patients should pay attention to their eyes. The main limitation of our study is the small patient population size. Multicenter data should be utilized in future studies.

Financial support and sponsorship

This work was supported by the grants from Beijing Municipal Administration of Hospitals' Ascent Plan (No. DFL20150201), the National Natural Science Foundation of China (Nos. 81570891 and 81272981), Beijing Natural Science Foundation (No. 7151003), Advanced Health Care Professionals Development Project of Beijing Municipal Health Bureau (No. 2014-2-003), Study on Individual Diagnosis and Therapy Strategy for Malignant Uveal Melanoma (No. 2016-1-2051), Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support (No. ZYLX201307), and Science and Technology Project of Beijing Municipal Science and Technology Commission (No. Z151100001615052).

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Xu L, Wang Y, Jonas JB. Incidence of nonarteritic anterior ischemic optic neuropathy in adult Chinese: The Beijing Eye Study. Eur J Ophthalmol 2007;17:459-60. doi: 10.1177/112067210701700335.  Back to cited text no. 1
    
2.
Wu S, Huang Z, Yang X, Zhou Y, Wang A, Chen L, et al. Prevalence of ideal cardiovascular health and its relationship with the 4-year cardiovascular events in a Northern Chinese industrial city. Circ Cardiovasc Qual Outcomes 2012;5:487-93. doi: 10.1161/circoutcomes.111.963694.  Back to cited text no. 2
    
3.
Kosanovic-Jakovic N, Ivanovic B, Milenkovic S, Risovic D, Dimitrijevic-Sreckovic V, Radosavljevic A, et al. Anterior ischemic optic neuropathy associated with metabolic syndrome. Arq Bras Oftalmol 2008;71:62-6. doi: 10.1590/S0004-27492008000100013.  Back to cited text no. 3
    
4.
Cheung N, Rogers S, Couper DJ, Klein R, Sharrett AR, Wong TY, et al. Is diabetic retinopathy an independent risk factor for ischemic stroke? Stroke 2007;38:398-401. doi: 10.1161/01.str.0000254547.91276.50.  Back to cited text no. 4
    
5.
Hayreh SS. Increased risk of stroke in patients with nonarteritic anterior ischemic optic neuropathy: A nationwide retrospective cohort study. Am J Ophthalmol 2017;175:213-4. doi: 10.1016/j.ajo.2016.12.010.  Back to cited text no. 5
    



 
 
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