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Article

Risk Factor Analysis of Early-Onset Cataracts in Taiwan

1
Department of Optometry, Chung Shan Medical University, Taichung 402, Taiwan
2
Department of Ophthalmology, Chung Shan Medical University Hospital, Taichung 402, Taiwan
3
Department of Optometry, Asia University, Taichung 402, Taiwan
4
Department of Special Education, National Taiwan Normal University, Taipei 106, Taiwan
*
Authors to whom correspondence should be addressed.
This author contributed equally to the main author.
J. Clin. Med. 2022, 11(9), 2374; https://doi.org/10.3390/jcm11092374
Submission received: 4 March 2022 / Revised: 16 April 2022 / Accepted: 22 April 2022 / Published: 23 April 2022
(This article belongs to the Special Issue Advances in Vision Disorders: Causes and Epidemiology)

Abstract

:
Purpose: According to previous studies, the prevalence rate of cataracts has increased in recent years. This study aims to investigate and analyze the risk factors of early-onset cataracts in Taiwan. Methods: A total of 71 subjects aged between 20 and 55 were diagnosed with cataracts in a medical center. Participants were divided into three groups: control, early-onset cataract (EOC), and combined (EOC combined with dry eye) groups. Eye examinations including autorefraction, best-corrected visual acuity (BCVA), subjective refraction, axial length, fundus, slit lamp, and reactive oxygen species (ROS, including total antioxidative capacity, TAC; C-reactive protein, CRP; and glutathione peroxidase, GPx) were performed. In addition, a questionnaire on patient information, history, habits, family history, and Depression Anxiety Stress Scales (DASS) was completed before the examination. Results: 27 non-EOC (control group), 20 EOC, and 24 combined patients participated in the study. Compared with the control group, Body Mass Index (BMI), gender, educational level, hypertension, diabetes, hyperlipidemia, chronic pain, and body-related diseases were significantly different between the three groups. Family history was also significantly different: family heart disease, hypertension, asthma, allergies, stroke, and immune system were also significantly different. In addition, subjects who took hypertensive drugs, antihistamines, and other medications were also significantly different. Statistical analysis indicated that best corrective visual acuity and the spherical equivalent were significantly different between the three groups. Similar results were found in CRP blood analysis. Discussion and Conclusion: According to the results, EOC may result from systemic diseases. The risk corresponded to an increase in ROS blood analysis. Furthermore, eye drops and medicine intake significantly influenced EOC patients. To prevent or defer early-onset cataracts, monitoring physical health, CRP, and GPx analysis may be worth considering in the future.

1. Introduction

Early-onset cataracts (EOCs) develop between the ages of 20 and 55 years old [1,2]. According to the Ministry of Health and Welfare statistics in 2018, cataracts are the most common eye disease in Taiwan’s ophthalmology clinic, with age-related cataracts accounting for 90.7% of cases, whereas the EOC group accounts for 9.07% [3,4]. The incidence of EOC increases year by year, with a younger age at diagnosis phenomenon [5,6]. Therefore, prevention and incidence reduction of EOC will be an important topic. Studies have found that the risk of complications such as Body Mass Index (BMI) [7], smoking [8,9], and alcohol consumption [10], hypertension, diabetes, hyperlipidemia, chronic obstructive pulmonary, asthma [11], stroke [12], ischemic heart disease [13], hypoparathyroidism [14], high myopia [15], and family disease [16] are associated with a higher risk of EOCs. In addition, research showed that people with EOCs increased their cumulative risk of all cancers, head and neck cancer, liver cancer, and breast cancer with increasing time of disease [17]. EOCs may not be a simple eye disease, such as the imbalance between the antioxidant capacity and oxidative stress, inflammation, metabolic-related syndromes, and genetic factors [18,19,20]. The above literature indicates that EOCs may require more attention than age-related cataracts.
Clinical experience and research results have also found that cataracts can cause a decline in functional vision, including contrast sensitivity, visual acuity, glare, photophobia, diplopia, and visual field, and can also lead to a decline in quality of life, occupation, academic performance, bicycle riding, behavioral performance, even mental or psychological state [21,22,23]. To sum up, cataracts are not only common in the elderly; cataracts tend to be in younger patients. Therefore, the purpose of this study was to investigate the possible risk factors of EOC.

2. Materials and Methods

A cross-sectional study was conducted from 11 November 2019 to 30 March 2020 in the Department of Ophthalmology, Cheng Ching Hospital, Taichung. All the procedures were in accordance with the Declaration of Helsinki. Approval was obtained from the Institutional Review Board of the Chung Shan Medical University Hospital (Taichung, Taiwan) (Approval number: CS18131). Due to the physical, spirit, and compliance, each subject may have taken several attempts to complete the examination. STROBE guidelines were used for reporting the manuscript [24,25].

2.1. Research Subjects

To investigate the risk factors associated with EOC, patients were all diagnosed by the same ophthalmologist between the ages of 20 and 55. Patients with congenital cataracts or other eye diseases or those unable to cooperate with this study were excluded. A total of 100 adults participated initially; 29 subjects were later excluded, one had a congenital cataract, five had experienced myopia surgery or retinal surgery, three had age-related degeneration, two had diabetic retinal disease, and 18 others dropped out or did not finish all examinations. Because a relatively high proportion of Taiwanese have dry eye syndrome, this study divided the patients with cataracts only into one group, and the patients with cataracts who were also diagnosed as early-stage dry eye syndrome by doctors as another group. The final total number of participants in this study was 71. Subjects were divided into three groups according to the ophthalmologist’s diagnosis, 27 non-EOC (control group), 20 EOC, and 24 combined group (EOC combined with dry eye) participated in the study. The ages of the three groups were significantly different (F = 3.76, p = 0.028), Tukey HDS comparison indicated that the EOC and combined groups were significantly older than the control group. Although the ages of the three groups of subjects were all within the age defined by early-onset cataracts, there was still an age gap, thus analysis must be conducted to control for age.

2.2. Research Materials

Variances in the study including autorefractor (NIDEK ARK-510A), objective refraction, distance visual acuity, non-contact intraocular pressure (IOP, non-contact Tonopachy NIDKE NT-530P), axial length (AL-Scan NIDEK 230488), slit lamp (TOPCON SL-7F), fundus and Optical Coherence Tomography (OCT. NIDEK RS-3000). In addition, total antioxidant blood included glutathione peroxidase (GPx), total antioxidative capacity (TAC), and C-reactive protein (CRP) were measured. Before the examination, a questionnaire was completed detailing each patient’s basic information, history, habit, family history, and Depression Anxiety Stress Scales (DASS).

2.3. Data Analysis and Statistical Analysis

The sample size of this study was determined using G*Power analysis, under effect size d = 0.5, α = 0.05, power (1-β) = 0.90. The calculated results of the total sample size were 70. All data were performed and analyzed using SPSS 22.0 statistical software (IBM, Armonk, NY, USA). A value of p < 0.05 was considered statistically significant. One-way ANOVA, Pearson χ2, and multi-logistic regression analyses were performed.

3. Results

To investigate the risk factors associated with EOC, subjects were all diagnosed by the same ophthalmologist between the ages of 20 and 55. The final effective number of participants was 71, and subjects were divided into three groups (27 control group, 20 EOC, and 24 combined group, Table 1) according to the ophthalmologist’s diagnosis. One-way ANOVA analysis indicated that the ages of the three groups were significantly different. The EOC group and the combined group were significantly older than the control group, following analysis must be conducted under controlling for age.

3.1. Background Possibility Risk Factors of EOC

3.1.1. Background Comparison between Groups

ANOVA analysis indicated no significant differences in participants’ height (F = 1.53, p = 0.22) or weight (F = 0.41, p = 0.66). However, Pearson χ2 analysis showed that gender (χ2 = 8.08, p = 0.04), BMI (χ2 = 6.89, p = 0.032), and educational level (χ2 = 6.33, p = 0.05) was significantly different between each group; females, those with a higher BMI, and those with a higher education level exhibited an increased risk of EOC.

3.1.2. Family History Comparison between Three Groups

Pearson χ2 analysis showed that family heart disease (χ2 = 6.06, p = 0.05), family hypertension (χ2 = 9.07, p = 0.01), family asthma (χ2 = 5.25, p = 0.04), family stroke (χ2 = 5.04, p = 0.04), familial immune system disease (χ2 = 4.44, p = 0.05), and family allergies (χ2 = 3.19, p = 0.02) were significantly difference between all three groups; the percentage in the EOC and combined groups were significantly higher than that in the control group. However, all familial eye diseases, such as family cataract, family glaucoma, and family diabetes did not reach statistical significance, as shown in Figure 1.

3.1.3. Healthy Status Comparison between Each Group

Pearson χ2 analysis showed that the subjects themselves who suffered from hypertension (χ2 = 10.50, p = 0.00), diabetes (χ2 = 4.80, p = 0.05), hyperlipidemia (χ2 = 5.25, p = 0.04), high myopia (χ2 = 4.67, p = 0.05), chronic pain (χ2 = 5.01, p = 0.04), and other illnesses (χ2 = 6.30, p = 0.04) were significantly different, the percentage in the EOC and combined groups were significantly higher than that in the control group; no statistically significant differences were determined in other diseases among the three groups (Table 2).

3.1.4. Lifestyle Habits and Drug Use Comparisons between Each Group

The results of the Pearson χ2 test for the lifestyle habits survey showed that there was no significant difference in smoking (χ2 = 3.816, p = 0.43), alcohol (χ2 = 0.686, p = 0.71), regular exercise (χ2 = 2.027, p = 0.36), use of mobile and computer (χ2 = 2.222, p = 0.33), coffee (χ2 = 2.379, p = 0.30), tea (χ2 = 0.112, p = 0.95), cola, or other refreshing drink (χ2 = 1.004, p = 0.60).
Pearson χ2 test of drug use also showed no significant differences in steroid (χ2 = 1.291, p = 0.53), amiodarone (χ2 = 2.586, p = 0.27), hormone (χ2 = 0.817, p = 0.67), or analgesics (χ2 = 2.523, p = 0.28); however, other medications, such as blood pressure (χ2 = 10.420, p = 0.00), antihistamines (χ2 = 4.804, p = 0.05), and other drugs (χ2 = 9.991, p = 0.01), were significantly different between the three groups. The EOC and combined groups received the higher proportion of anti-hypertensive, antihistamine, and other drugs (Table 3).

3.2. Psychological Possibility Risk Factors of EOC

The DASS questionnaire was used to determine subjects that had experienced psychological problems. Pearson χ2 analysis showed that the subjects diagnosed as EOC or combined group had significantly higher levels of anxiety (χ2 = 18.524, p = 0.018) and stress (χ2 = 20.368, p = 0.002) than the control group. At the same time, depression (χ2 = 8.563, p = 0.380) was insignificant (Figure 2).

3.3. Blood Possibility Risk Factors of EOC

Blood analysis determined that there were no significant differences in GPx (χ2 = 1.267, p = 0.53) or TAC (χ2= 1.512, p = 0.47); while CRP index (χ2 = 7.856, p = 0.02) showed a significant difference between all three groups; the percentage in the EOC and combined groups were much higher than that in the control group, as shown in Table 4. A C-reactive protein (CRP) test measured the level of C-reactive protein in blood. CRP is a protein made by the liver and excreted into the bloodstream in response to inflammation which may protect tissues during injury or infection.

3.4. Visual Function Possibility Risk Factors of EOC

Visual function examination included refractive errors, axial length, cup to disc ratio (CD ratio), intraocular pressure (IOP), and visual acuity. Since the data from the left and right eyes are not significantly different, the data of ocular physiology are mainly from the right eye. ANOVA analysis showed significant differences in best correct visual acuity (F = 22.95, p = 0.00) and spherical equivalent (F = 3.26, p = 0.04), but did not show significant difference in astigmatic (F = 0.24, p = 0.79), IOP (F = 0.946, p = 0.393), CD ratio (F = 0.308, p = 0.74), or axial length (F = 2.24, p = 0.12).
In summary, (1) family disease, such as family heart disease, hypertension, asthma, stroke, immune system diseases, and allergies; (2) patients’ background, BMI, gender, education level, best corrective visual acuity (BCVA), spherical equivalent; or (3) patients themselves suffered from hypertension, diabetes, hyperlipidemia, and chronic pain; drug use for blood pressure, antihistamines, anxiety, stress, or even the detection of CRP index in the blood are helpful to detect EOC, which is a topic worthy of discussion.

3.5. Linear Regression Analysis on Predicting EOC

The risk factor analysis of patients with EOC in Taiwan was based on the basic information of the research subjects, health status survey, living habits survey, anxiety scale, eye examination, and blood analysis that had shown significant differences using ANOVA and Chi-square analysis as independent variables. In addition, the preoperative group was subjected to multinomial logistic regression analysis as the dependent variable to predict the risk factors of EOC with higher explanatory power (Table 5 and Table 6).
The multinomial logistic regression analysis showed that for the background variables (χ2 = 9.889, p = 0.042, Cox R2 = 0.125), family disease (χ2 = 35.470, p = 0.003, Cox R2 = 0.341), healthy status (χ2 = 48.972, p= 0.00, Cox R2= 0.438), medication (χ2 = 39.619, p = 0.001, Cox R2 = 0.373), psychology (χ2 = 13.510, p= 0.009, Cox R2 = 0.149), blood (χ2 = 7.452, p= 0.024, Cox R2 = 0.170), and eye examination (χ2 = 18.685, p = 0.001, Cox R2 = 0.215), each dimension had good and significant predictive ability for EOC. The overall variable can explain up to 88.2% of EOC (χ2 = 72.990, p = 0.004, Cox R2 = 0.883). Strong predictors after screening included BMI, educational level, family heart disease, family hypertension, family allergies, high myopia, other illness, other drugs taken, stress, CRP, BCVA, and spherical equivalent. For example, while the stress index increased by one unit, the risk of developing EOC was 3.258 higher than the control group.

4. Discussion

Among the background data, the ages of the three groups were significantly different. The EOC group and combined group were significantly older than the control group. In addition, a higher BMI value, females, and highly educated subjects represented a higher proportion of those suffering from EOC [26,27]. Most participants were excluded at the beginning due to being diagnosed with eye-related diseases or having experienced eye-related surgery. Patients with eye-related diseases or having experienced eye-related surgery had a high proportion of EOC, among which retinal diseases and retinal surgery have the greatest impact. In the family history, relatives with heart disease, hypertension, asthma, stroke, immune system diseases, and allergic constitution have a high proportion of EOC, among which family heart disease, family hypertension, and family allergies have the greatest impact [28,29]. The physiological mechanism of genes, genetic inheritance, environment, and diet remains to be clarified.
In the health survey of the subjects themselves, the patients themselves were suffering from hypertension, diabetes, hyperlipidemia, high myopia, chronic pain, and abnormal CRP index in the blood analysis. A higher proportion of patients with EOC had the most significant impact on other physical illnesses and CRP values [1,30,31,32,33,34,35]. It is reasonable that people with a high BMI are more likely to have symptoms such as high blood sugar, blood pressure, and high blood lipids, so the risk of developing cataracts is higher than that of the normal BMI group. However, there have been no reports to determine whether monitoring the C-reactive protein index is helpful to delay or detect EOC [32,33,34,35]; a relevant topic for future discussion.
In terms of medication, patients with EOC used a high proportion of blood pressure lowering drugs, antihistamines, and other drugs [26,27]. It is worth noting that a high proportion of patients with EOC take antihistamine drugs, which may cause oxidative pressure due to long-term inflammation of the body, which may indirectly lead to the formation of cataracts [28,29].
In examining ophthalmology and optometry, the best corrective visual acuity, spherical equivalent, has a high proportion of patients with early-onset cataracts, and the BCVA before cataract surgery has the greatest impact [36,37]. Although the CD ratio did not show significant differences between groups, previous literature indicated a high proportion of patients with EOC have abnormal CD values, which is related to patients which have also been diagnosed with glaucoma. According to Law and Wang [38], glaucoma is complicated by cataracts, and may compress the optic nerve to cause abnormal CD values. However, at present, the relationship between glaucoma and EOC has yet to be directly linked.
Psychological stress and anxiety are also risk factors for EOC, and the ability of stress to predict EOC is noteworthy. However, there is very little relevant literature to directly point out whether the stress variable in the anxiety scale can be applied to the detection of EOC or whether it will improve the incidence of EOC [23]; a topic worthy of discussion in the future.

5. Conclusions

This study found that BMI, gender, education level, preoperative visual acuity, family history of heart disease, hypertension, asthma, apoplexy, immune system diseases, and allergic constitution, and people themselves having hypertension, diabetes, hyperlipidemia, and chronic pain disorders, in addition to taking anti-hypertensive medicine and antihistamines had a high proportion of EOCs. Furthermore, the detection of CRP index in blood, BCVA, and myopia control helped detect EOC, which is also an important topic worthy of follow-up discussion. Although, as mentioned above, the physiological mechanism of genes, genetic inheritance, environment, and diet remains to be clarified, it is suggested that in the future, the government should support the funds to the ophthalmic medical association and should be expanded to carry out research in various regions of the country with more research samples to obtain more research results, and carry out a synchronous analysis with the health insurance database, which will be the research direction in the future.

Author Contributions

Conceptualization, C.-Y.C. and. C.-J.L.; investigation, data curation, and formal analysis, C.-Y.C., C.-J.L. and S.-P.L.; writing—original draft preparation, C.-Y.C., H.-P.H. and L.-H.T.; writing—review and editing, C.-Y.C., C.-C.C., H.-P.H. and L.-H.T. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Chung Shan Medical University Hospital research 327 project (CHS-2019-C-038) in Taiwan.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Ethics Committee of Chung Shan Medical University Hospital (Taichung, Taiwan) (approval number: CS18131).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The datasets used during the current study are available from the corresponding author.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

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Figure 1. Family history disease prevalence between each group under controlling of age variance.
Figure 1. Family history disease prevalence between each group under controlling of age variance.
Jcm 11 02374 g001
Figure 2. Psychological status of DASS-42 between each group.
Figure 2. Psychological status of DASS-42 between each group.
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Table 1. Patient gender and age characteristics for each experimental group.
Table 1. Patient gender and age characteristics for each experimental group.
Number%GenderNumberAverage of Age
Control group2738.0%Male 1245.17 ± 9.722
Female1544.60 ± 4.388
Early-onset cataract
(EOC)
2028.2%Male 1249.92 ± 3.679
Female849.75 ± 4.464
Combined group
(EOC + dry eye)
2433.8%Male 949.33 ± 3.536
Female1549.40 ± 6.390
Table 2. Health status analysis using Pearson χ2 for each group.
Table 2. Health status analysis using Pearson χ2 for each group.
Controlling
Age Variance
GroupsPearson χ2p
NormalCataractCombined
Hypertensionyes07610.4950.00 **
0.0%35.0%25.0%
no271318
100.0%65.0%75.0%
Diabetesyes0344.7990.05 *
0.0%15.0%16.7%
no271720
100.0%85.0%83.3%
Asthmayes1110.0480.98
3.7%5.0%4.2%
no261923
96.3%95.0%95.8%
Hyperlipidemiayes0205.2480.04 *
0.0%10.0%0.0%
no271824
100.0%90.0%100.0%
Immune system diseaseyes1110.0480.98
3.7%5.0%4.2%
no261923
96.3%95.0%95.8%
Canceryes1010.8170.66
3.7%0.0%4.2%
no262023
96.3%100.0%95.8%
High myopiayes101283.6650.16
37.0%60.0%33.3%
no17816
63.0%40.0%66.7%
High astigmatismyes1202.7250.26
3.7%10.0%0.0%
no261824
96.3%90.0%100.0%
Thyroid dysfunctionyes1220.7880.67
3.7%10.0%8.3%
no261822
96.3%90.0%91.7%
Galactosemiayes0102.5860.27
0.0%5.0%0.0%
no271924
100.0%95.0%100.0%
Homo cystinuriayes0011.9860.37
0.0%0.0%4.2%
no272023
100.0%100.0%95.8%
Migraineyes3461.6920.43
11.1%20.0%25.0%
no241618
88.9%80.0%75.0%
Irritable Bowel Disorderyes2021.6830.43
7.4%0.0%8.3%
no252022
92.6%100.0%91.7%
Chronic painyes0315.0090.04 *
0.0%15.0%4.2%
no271723
100.0%85.0%95.8%
Head injuryyes1211.0040.61
3.7%10.0%4.2%
no261823
96.3%90.0%95.8%
Other illnessesyes3896.2990.04 *
11.1%40.0%37.5%
no241215
88.9%60.0%62.5%
* p < 0.05, ** p < 0.01.
Table 3. Pearson χ2 analysis on the health status between groups.
Table 3. Pearson χ2 analysis on the health status between groups.
Controlling
Age Variance
GroupsPearson χ2p
NormalCataractCombined
Steroidyes1221.2910.53
3.7%10.0%8.3%
no261822
96.30%90.00%91.70%
Anti-hypertensive drug pressureyes07510.4200.00 **
0.0%35.0%20.8%
no271319
100.0%65.00%79.20%
Amiodaroneyes0102.5860.27
0.0%5.0%0.0%
no271924
100.0%95.0%100.0%
Antihistamineyes1414.8040.05
3.7%20.0%4.2%
no261623
96.3%80.0%95.8%
Hormone therapyyes1010.8170.67
3.7%0.0%4.2%
no262023
96.3%100.0%95.8%
Painkilleryes1342.5230.28
3.7%15.0%16.7%
no261720
96.3%85.0%83.3%
Other drugsyes4769.9910.01 *
14.8%35.0%25.0%
no231318
85.2%65.0%75.0%
* p < 0.05, ** p < 0.01.
Table 4. Pearson χ2 analysis of blood results between each group.
Table 4. Pearson χ2 analysis of blood results between each group.
Controlling
Age Variance
GroupsPearson χ2p
NormalCataractCombined
GPx indexnormal127131.2670.53
80.0%77.8%92.9%
abnormal321
20.0%22.2%7.1%
CRP indexnormal15787.8560.02 *
100.0%70.0%57.1%
abnormal036
0.0%30.0%42.9%
TAC indexnormal107121.5120.47
66.7%70.0%85.7%
abnormal532
33.3%30.0%14.3%
* p < 0.05; total antioxidative capacity, TAC; C-reactive protein, CRP; glutathione peroxidase, GPx.
Table 5. Multinomial logistic regression analysis in each dimension (controlling age variance).
Table 5. Multinomial logistic regression analysis in each dimension (controlling age variance).
Dimensionχ2pCox R2
Background9.8890.0420.125
Family disease35.4700.0030.341
Healthy status48.9720.0000.438
Medication39.6190.0010.373
Psychology13.5100.0090.149
Blood7.4520.0240.170
Eye examination18.6850.0010.215
Overall72.9900.0040.883
Table 6. Multinomial logistic regression analysis between each group.
Table 6. Multinomial logistic regression analysis between each group.
BS.E.Waldp-ValueExp(B)
BMIEOC vs. Control−1.0430.6062.9610.0850.352
Combined vs. Control−1.8730.6488.3570.004 **0.154
Educational levelEOC vs. Control−1.4560.7333.9490.047 *0.233
Combined vs. Control−1.7550.7305.7850.016 *0.173
Family heart diseaseEOC vs. Control−2.1650.9874.8120.028 *0.115
Combined vs. Control−1.4561.0252.0180.1550.233
Family hypertensionEOC vs. Control−1.4200.6514.7600.029 *0.242
Combined vs. Control−0.7800.6201.5800.2090.459
Family allergiesEOC vs. Control−1.1330.7722.1550.1420.322
Combined vs. Control−1.6790.7754.6990.030 *0.187
High myopiaEOC vs. Control−1.9500.7586.6250.010 *0.142
Combined vs. Control−1.4420.6165.5150.019 *0.143
Other illnessEOC vs. Control−1.9000.8305.2350.022 *0.150
Combined vs. Control−1.6970.7325.3670.021 *0.183
Other drugsEOC vs. Control−1.6770.8803.6350.0570.187
Combined vs. Control−1.3030.7952.6840.1010.272
StressEOC vs. Control1.1820.5045.5050.019 *3.259
Combined vs. Control0.8500.4803.1310.0772.339
CRPEOC vs. Control6.3073.6892.9230.087548.43
Combined vs. Control6.3373.6573.0030.083565.38
BCVAEOC vs. Control−12.2075.6204.7180.030 *0.005
Combined vs. Control−7.8115.9941.6980.1930.033
Spherical equivalentEOC vs. Control0.3390.1495.1810.023 *1.404
Combined vs. Control0.2420.1065.2020.023 *1.274
* p < 0.05, ** p < 0.01; body mass index (BMI); C-reactive protein (CRP); best corrective visual acuity (BCVA).
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Tsai, L.-H.; Chen, C.-C.; Lin, C.-J.; Lin, S.-P.; Cheng, C.-Y.; Hsieh, H.-P. Risk Factor Analysis of Early-Onset Cataracts in Taiwan. J. Clin. Med. 2022, 11, 2374. https://doi.org/10.3390/jcm11092374

AMA Style

Tsai L-H, Chen C-C, Lin C-J, Lin S-P, Cheng C-Y, Hsieh H-P. Risk Factor Analysis of Early-Onset Cataracts in Taiwan. Journal of Clinical Medicine. 2022; 11(9):2374. https://doi.org/10.3390/jcm11092374

Chicago/Turabian Style

Tsai, Lung-Hui, Ching-Chung Chen, Chien-Ju Lin, Sheng-Pei Lin, Ching-Ying Cheng, and Hsi-Pao Hsieh. 2022. "Risk Factor Analysis of Early-Onset Cataracts in Taiwan" Journal of Clinical Medicine 11, no. 9: 2374. https://doi.org/10.3390/jcm11092374

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