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. 2023 Jun 5;23:251. doi: 10.1186/s12886-023-03009-w

Prevalence and predictors of vision impairment among older adults in India: evidence from LASI, 2017–18

Shobhit Srivastava 1, Manish Kumar 1, T Muhammad 1,, Paramita Debnath 1
PMCID: PMC10240694  PMID: 37277715

Abstract

Background

Older adults experience a natural decline in health, physical and cognitive functionality, and vision impairment (VI) is one among them and has become an increasing health concern worldwide. The present study assessed the association of chronic morbidities such as diabetes, hypertension, stroke, heart diseases and various socioeconomic factors with VI among older Indian adults.

Methods

Data for this study were derived from the nationally-representative Longitudinal Ageing Study in India (LASI), wave-1 (2017–18). VI was assessed using the cut-off of visual acuity worse than 20/80, and additional analysis was carried out using the definition of VI with a cut-off of visual acuity worse than 20/63. Descriptive statistics along with cross-tabulation were presented in the study. Proportion test was used to evaluate the significance level for sex differentials in VI among older adults. Additionally, multivariable logistic regression analysis was conducted to explore the factors associated with VI among older adults.

Results

About 33.8% of males and 40% of females suffered from VI in India (visual acuity worse than 20/80). Meghalaya (59.5%) had the highest prevalence for VI among older males followed by Arunachal Pradesh (58.4%) and Tripura (45.2%). Additionally, Arunachal Pradesh (77.4%) had the highest prevalence for VI among females followed by Meghalaya (68.8%) and Delhi (56.1%). Among the health factors, stroke [AOR: 1.20; CI: 1.03–1.53] and hypertension [AOR: 1.12; CI: 1.01–1.22] were the significant risk factors for VI among older adults. Additionally, being oldest old [AOR: 1.58; CI: 1.32–1.89] and divorced/separated/deserted/others [AOR: 1.42; CI: 1.08–1.87] were significantly associated with VI. Moreover, older adults with higher educational status [AOR: 0.42; CI: 0.34, 0.52], currently working [AOR: 0.77; CI: 0.67, 0.88], from urban areas [AOR: 0.86; CI: 0.76–0.98] and from western region [AOR: 0.55; CI: 0.48–0.64] had lower odds of VI in this study.

Conclusion

This study identified higher rates of VI among those who are diagnosed with hypertension or stroke, currently unmarried, socioeconomically poorer, less educated and urban resident older people that can inform strategies to engage high risk groups. The findings also suggest that specific interventions that promote active aging are required for those who are socioeconomically disadvantaged as well as visually impaired.

Supplementary Information

The online version contains supplementary material available at 10.1186/s12886-023-03009-w.

Keywords: Vision impairment, Chronic condition, Socioeconomic, Older adult, India

Background

Older adults experience a natural decline in health, physical and cognitive functionality [1]. Visual impairment (VI) is one among them and has become an increasing health concern worldwide [2]. Globally, about 295 million people of all ages have problems related to vision and 43 million people are estimated to be blind, although constant global initiatives had extended reduction in cases of avoidable blindness, but the prevalence of low vision is expected to double during the next 30 years and the global burden is expected to increase in line as the population ages [3, 4]. The top three causes of most severe vision loss among adults aged 50 years and above are cataract, refractive errors and glaucoma that are avoidable through comprehensive eye tests, surgery, medications and spectacle corrections early in the disease progression which can delay or prevent 80% of the cases of VI [5]. Studies suggested the prevalence of blindness due to mentioned causes to be substantially higher in countries like East Asia, South East Asia and Sub-Saharan Africa compared to high-income sub-regions (2). Low vision on the other hand, has significant impact on lives of millions of older adults and poses serious challenges on person’s independence, mobility, usual activities of daily living and poor quality of life [6, 7]. It is therefore a pressing issue that needs urgent attention because of its complex and far-reaching impacts on both older adults and society as a whole especially in developing countries [8].

The effect of deteriorating general health with old age is often interwoven with loss/weakening of vision [9]. Multiple comorbidities existing with VI generally appear to have important implication on health care and rehabilitation services for older adults [10]. Notably, diabetes, hypertension, heart diseases are few most prevalent conditions among older adults [11]. Some of these comorbidities are also frequently observed in older adults with VI [10]. Studies have also suggested other associated factors such as poverty, inadequate access to basic amenities and malnutrition to be significant for low vision/complete loss of vision. Similarly, several cross-sectional studies in India, indicated prevalence of VI and higher risk of morbidities and mortality, widely distinctive based on different sex and socio-economic circumstances of an older adult [12], for instance, older women are often more likely to have VI [13], while, evidences are inconclusive as some suggest women are over represented in the VI group compared to men [10]. There is substantial evidence from developing countries, where, only small proportion of older adults aged 65 and above have financial independence, higher education and employment as factors consistently associated with being at higher risk of VI [8].

So far, VI had been mostly characterised as an age-related problem due to systemic and sensory changes majorly influencing loss of vision among older people [14]. The information on various risk factors of VI among older adults is important to quantify the unmet needs for eye care services, especially in resource-limited settings including India, so that early detection, diagnosis and treatment can be facilitated for older individuals with reduced vision in a community. The current study assessed the association of chronic morbidities such as diabetes, hypertension, stroke, heart diseases and various socioeconomic factors with VI using data from the Longitudinal Ageing Study in India (LASI, wave-1). Also, regional differences in the prevalence of VI among older adults are explored in this study.

Methods

Data

Data for this study were derived from the nationally-representative LASI, wave-1 [15]. LASI is a full-scale national survey of scientific investigation of the health, economic, and social determinants and consequences of population aging in India, conducted in 2017–18. The LASI is a nationally representative survey over 72,000 older adults age 45 and above across all states and union territories of India. The main objective of the survey is to study the health status and the social and economic well-being of older adults in India. LASI adopted a multistage stratified area probability cluster sampling design to arrive at the eventual units of observation: older adults age 45 and above and their spouses irrespective of age [15]. The survey adopted a three-stage sampling design in rural areas and a four-stage sampling design in urban areas. In each state/UT, the first stage involved the selection of Primary Sampling Units (PSUs), that is, sub-districts (Tehsils/Talukas), and the second stage involved the selection of villages in rural areas and wards in urban areas in the selected PSUs. In rural areas, households were selected from selected villages in the third stage. However, sampling in urban areas involved an additional stage [15]. Specifically, in the third stage, one Census Enumeration Block (CEB) was randomly selected in each in urban area. In the fourth stage, households were selected from this CEB. The detailed methodology, with the complete information on the survey design and data collection, was published in the survey report [15]. The present study is conducted on the eligible respondent’s age 60 years and above. The total sample size for the present study is 31,464 (15,098 male and 16,366 female) elders aged 60 years and above [15].

Variable description

Outcome variable

In LASI, for all participants, near vision and distance vision was measured for both eyes with the best possible correction available. According to the world health organization (WHO), International Classification of Diseases (ICD)- 10th Revision: vision impairment is defined as presenting visual acuity of less than 6/18 in the better eye with available correction. A screen of computer-assisted personal interviewing (mini laptop CAPI device)—based tumbling E log MAR (Logarithm of the Minimum Angle of Resolution) chart was used for the vision-related measurements [15]. As per the standard protocol, the near vision and distance vision was measured at 40 cm and 3 m, respectively [16]. In the E log MAR chart, the scale orientations used for near vision were 20/20, 20/25, 20/32, 20/40, 20/50, 20/63, 20/80, 20/125, 20/160, 20/250, 20/320, and 20/400, and for distance vision were 20/20, 20/25, 20/32, 20/40, 20/50, 20/63, 20/80, 20/125, 20/160, 20/250, and 20/320. The low near vision is defined as the “near vision equal to or poorer than 20/80 and equal to or better than 20/400 in the better eye”. On the other hand, low distant vision is defined as the “distance vision equal to or poorer than 20/80 and equal to or better than 20/200 in the better eye” [15, 17]. Finally, visual impairment (VI) includes both the near and distance low vision, and older adults were categorised as visually impaired if they had either low near vision or low distant vision. For the sensitivity analysis, VI was also measured using the cut-point of a visual acuity worse than 20/63, according to the World Health Organization criteria (Supplementary material). Moreover, a visual acuity of less than 20/400 (3/60) in the better eye and being unable to count fingers or perceive light have been considered blind.

Covariates

Diabetes, hypertension, stroke and heart disease were coded as no and yes. The variables were created based on the question “Has any health professional ever diagnosed you with the following diseases?” The response was categorized as 0 “no” and 1 “yes”. Such patient-reported outcome measures (PROM) do have their salience in this particular context [18].

According to the studies mentioned above, several socio-demographic variables were selected and included in this study. Age was categorized as young old (60–69 years), old-old (70–79 years) and oldest-old (80 + years). Sex was categorized as male and female. Education was categorized as no education, primary, secondary and higher. Marital status was categorized as currently married, widowed and others (divorced/ separated/ deserted/ never married). Working status was categorized as working, retired and not working [19]. Current tobacco (smoke and chew) users were categorized as no and yes. The ever use of alcohol in lifetime was categorised as no and yes.

Monthly per capita expenditure (MPCE) quintile was estimated using household consumption data. The details of the measure are provided in the survey report [15]. The variable was divided into five quintiles i.e., from poorest to richest. Religion was categorized as Hindu, Muslim, Christian and Others. Caste was categorized as Scheduled Tribe, Scheduled Caste, Other Backward Class and others. The Scheduled Caste includes a group of population which is socially segregated and financially/economically by their low status as per Hindu caste hierarchy. The Scheduled Castes (SCs) and Scheduled Tribes (STs) are among the most disadvantaged socio-economic groups in India. The OBC are the group of people who were identified as “educationally, economically and socially backward”. The OBCs are considered low in traditional caste hierarchy [20]. The “others” category is identified as people having higher social status. Place of residence was categorized as rural and urban. Regions were coded as North, Central, East, Northeast, West and South.

Statistical analysis

Descriptive statistics along with cross-tabulation were presented in the present study. Proportion test was used to evaluate the significance level for gender differentials in VI among older adults [21]. Additionally, multivariable logistic regression analysis [22] was used to establish the association between the outcome variable (VI) and other explanatory variables. The estimates provided are adjusted odds ratio (AOR) as they will be adjusted for the selected background characteristics.

The binary logistic regression model is usually put into a more compact form as follows:

LogitPY=1=β0+βX

The parameter β0 estimates the log odds of VI for the reference group, while β estimates the maximum likelihood, the differential log odds of VI associated with a set of predictors X, as compared to the reference group. Variance inflation factor (VIF) was generated in STATA 14 [23] to check the multicollinearity and there was no evidence of multicollinearity in the variables used [24, 25] (Supplementary Table S1). Additionally, individual weights were used which were present in the dataset to make the estimates nationally representative.

Results

Table 1 represents sample characteristics of the study population. Nearly 16.3% of older males and 14.8% of older females suffered from diabetes. About 30.8% of older males and 38.9% of older females suffered from hypertension. Nearly 3.3% and 5.9% of older males and 2.1% and 4.2% of older females suffered from stroke and heart diseases respectively. Almost, 36.3% of older males and 69% of older female were not educated, whereas, about 12.1 older males and 3.5% older females had higher educational status. Nearly, 15.2% of older males and 51.5% of older females were widowed. Almost 5% and 49% of older males and older females never worked. About 24.5% and 23.3% of older males and 4.3% and 15.5% of older females smoked tobacco and chewed tobacco, respectively. Also, nearly 31.3% of older males and 4.2% of older females consumed alcohol.

Table 1.

Sample characteristics of the study population, India, LASI Wave 1, 2017–18

Background characteristics Male Female Total
n % n % n %
Diabetes
 No 12,594 83.7 13,927 85.2 26,521 84.5
 Yes 2,444 16.3 2,416 14.8 4,860 15.5
Hypertension
 No 10,401 69.2 9,986 61.1 20,387 65.0
 Yes 4,640 30.8 6,355 38.9 10,995 35.0
Stroke
 No 14,546 96.7 15,994 97.9 30,540 97.3
 Yes 495 3.3 347 2.1 842 2.7
Heart Disease
 No 14,155 94.1 15,656 95.8 29,811 95.0
 Yes 886 5.9 686 4.2 1,572 5.0
Age group (in years)
 Young-old (60–69) 8,961 59.4 10,013 61.2 18,974 60.3
 Old-old (70–79) 4,545 30.1 4,556 27.8 9,101 28.9
 Oldest-old (80 +) 1,592 10.5 1,797 11.0 3,389 10.8
Education
 No education 5479 36.3 11,410 69.7 16,889 53.7
 Primary 4479 29.7 3,081 18.8 7,560 24.0
 Secondary 3307 21.9 1,307 8.0 4,614 14.7
 Higher 1833 12.1 568 3.5 2,401 7.6
Marital status
 Currently married 12,398 82.1 7,522 46.0 19,920 63.3
 Widowed 2,293 15.2 8,426 51.5 10,719 34.1
 Othersa 407 2.7 418 2.6 825 2.6
Working status
 Never worked 755 5.0 8,021 49.0 8776 27.9
 Currently working 6,331 41.9 2,976 18.2 9307 29.6
 Not currently working 8,008 53.1 5,365 32.8 13,373 42.5
Currently smoke tobacco
 No 11,274 75.5 15,557 95.7 26,831 86.0
 Yes 3,667 24.5 706 4.3 4,373 14.0
Currently chew tobacco
 No 11,461 76.7 13,749 84.5 25,210 80.8
 Yes 3,480 23.3 2,514 15.5 5,994 19.2
Alcohol consumption
 No 10,263 68.7 15,583 95.8 25,846 82.8
 Yes 4,679 31.3 685 4.2 5,364 17.2
MPCE quintile
 Poorest 3,035 20.1 3,449 21.1 6,484 20.6
 Poorer 3,068 20.3 3,409 20.8 6,477 20.6
 Middle 3,064 20.3 3,352 20.5 6,416 20.4
 Richer 2,990 19.8 3,180 19.4 6,170 19.6
 Richest 2,941 19.5 2,976 18.2 5,917 18.8
Religion
 Hindu 11,078 73.4 11,959 73.1 23,037 73.2
 Muslim 1,804 11.9 1,927 11.8 3,731 11.9
 Christian 1,468 9.7 1,682 10.3 3,150 10.0
 Othersb 748 5.0 797 4.9 1,545 4.9
Caste
 Scheduled Caste 2,448 16.7 2,692 17.1 5,140 16.9
 Scheduled Tribe 2,436 16.6 2,737 17.3 5,173 17.0
 Other Backward Class 5,781 39.5 6,105 38.7 11,886 39.1
 Others 3,970 27.1 4,248 26.9 8,218 27.0
Place of residence
 Rural 10,077 66.7 10,648 65.1 20,725 65.9
 Urban 5,021 33.3 5,718 34.9 10,739 34.1
Region
 North 2,799 18.5 3,013 18.4 5,812 18.5
 Central 2,155 14.3 2,107 12.9 4,262 13.6
 East 2,863 19.0 2,894 17.7 5,757 18.3
 Northeast 1,782 11.8 1,970 12.0 3,752 11.9
 West 1,953 12.9 2,350 14.4 4,303 13.7
 South 3,546 23.5 4,032 24.6 7,578 24.1
Overall 15,098 100.0 16,366 100.0 31,464 100.0

a Includes Divorced/Separated/Deserted/Others

b Includes Sikh, Buddhist/neo-Buddhist, Jain, Jewish, and Parsi/Zoroastrian

Table 2 represents the age-sex adjusted and unadjusted prevalence of VI among older adults in India, 2017–2018 (visual acuity worse than 20/80). About 37.1% of older adult had VI when unadjusted for age and sex. However, about 37.6% of older adult had VI when adjusted for age and sex. As documented in Supplementary Table S1, the values were much higher when VI was measured with a cut-off of worse than 20/63 (64.7% in the unadjusted and 64.1% in the adjusted estimates).

Table 2.

Age-sex adjusted and unadjusted prevalence of VI among older adults in India, 2017–2018

Unadjusted Adjusted
% CI % CI
Overall 37.1 (36.50, 37.62) 37.6 (37.05, 38.16)
Diabetes
 No 38.8 (37.62, 38.85) 38.6 (37.96, 39.18)
 Yes 32.1 (28.72, 31.43) 32.4 (30.99, 33.77)
Hypertension
 No 38.2 (36.49, 37.88) 38.5 (37.81, 39.20)
 Yes 36.8 (35.88, 37.78) 35.9 (34.99, 36.87)
Stroke
 No 37.7 (36.41, 37.54) 37.5 (36.98, 38.11)
 Yes 40.3 (36.85, 44.15) 40.4 (36.61, 44.13)
Heart Disease
 No 38.0 (36.76, 37.91) 37.9 (37.27, 38.42)
 Yes 32.9 (29.71, 34.55) 33.5 (31.08, 35.99)
Education
 No education 44.3 (41.75, 43.32) 43.3 (42.43, 44.10)
 Primary 35.4 (34.39, 36.64) 36.0 (34.84, 37.16)
 Secondary 26.4 (24.04, 26.68) 27.6 (25.94, 29.30)
 Higher 20.2 (18.68, 22.12) 21.8 (19.45, 24.15)
Marital status
 Currently married 34.7 (33.80, 35.19) 36.8 (36.00, 37.60)
 Widowed 43.4 (40.10, 42.07) 40.1 (38.86, 41.40)
 Othersa 38.7 (40.36, 47.60) 38.7 (35.12, 42.28)
Working status
 Never worked 42.7 (40.49, 42.67) 42.4 (40.45, 44.43)
 Currently working 34.0 (31.54, 33.53) 38.3 (36.91, 39.62)
 Not currently working 37.1 (36.76, 38.49) 36.7 (35.78, 37.57)
Currently smoke tobacco
 No 37.9 (36.91, 38.13) 37.2 (36.58, 37.79)
 Yes 36.7 (32.86, 35.79) 40.4 (38.25, 42.44)
Currently chew tobacco
 No 37.4 (36.38, 37.64) 37.0 (36.41, 37.65)
 Yes 39.1 (36.02, 38.56) 40.2 (38.87, 41.48)
Alcohol consumption
 No 37.9 (36.68, 37.92) 36.9 (36.32, 37.56)
 Yes 36.8 (34.35, 37.02) 41.7 (39.55, 43.78)
MPCE quintile
 Poorest 41.1 (38.99, 41.51) 40.9 (39.68, 42.2)
 Poorer 39.8 (38.62, 41.13) 39.6 (38.34, 40.82)
 Middle 38.4 (35.33, 37.79) 38.3 (37.04, 39.50)
 Richer 36.0 (32.66, 35.14) 35.8 (34.53, 37.02)
 Richest 32.9 (32.25, 34.79) 33.0 (31.79, 34.28)
Religion
 Hindu 37.2 (36.34, 37.65) 37.1 (36.44, 37.74)
 Muslim 35.0 (33.53, 36.75) 35.1 (33.55, 36.74)
 Christian 42.7 (40.03, 43.66) 42.2 (40.35, 43.94)
 Othersb 42.3 (38.02, 43.20) 42.0 (39.38, 44.56)
Caste
 Scheduled Caste 42.0 (40.23, 43.06) 42.1 (40.73, 43.56)
 Scheduled Tribe 43.5 (39.12, 41.93) 43.4 (41.99, 44.79)
 Other Backward Class 36.3 (35.36, 37.17) 36.2 (35.32, 37.11)
 Others 33.2 (32.57, 34.73) 32.8 (31.77, 33.89)
Place of residence
 Rural 40.7 (38.80, 40.19) 40.6 (39.88, 41.26)
 Urban 31.8 (30.02, 31.88) 31.7 (30.81, 32.67)
Region
 North 39.5 (40.45, 43.1) 39.3 (38.01, 40.60)
 Central 35.9 (35.26, 38.31) 35.9 (34.41, 37.43)
 East 39.2 (39.10, 41.74) 39.2 (37.93, 40.53)
 Northeast 48.2 (47.68, 51.06) 47.6 (45.93, 49.25)
 West 29.5 (25.70, 28.54) 29.7 (28.23, 31.14)
 South 35.6 (35.52, 37.81) 35.4 (34.25, 36.51)

a Includes Divorced/Separated/Deserted/Others

b Includes Sikh, Buddhist/neo-Buddhist, Jain, Jewish, and Parsi/Zoroastrian

Prevalence (%) of VI among older adults, stratified by sex, according to their background characteristics is presented in Table 3 (visual acuity worse than 20/80). Older males (39.7%) and females (41.5%) who suffered from stroke had higher prevalence of VI. Oldest old males (47.8%) and females (47.4%) had higher prevalence of VI. Older males and females with no formal education had higher prevalence of VI. Older males (44.7%) and females (41.4%) who never worked had higher prevalence of VI. Older males (34.8%) and females (44.5%) who consumed alcohol had higher prevalence of VI. Older male and females from lower socio-economic groups i.e., from poorest MPCE quintile, Scheduled Caste and with a rural residence had higher prevalence of VI. Additionally, older females had significantly higher prevalence of VI than older males (Difference: -6.2%; p < 0.001). The prevalence of VI stratified by sex according to the cut-off of visual acuity worse than 20/63 is presented in Table S2.

Table 3.

Prevalence (%) of VI among older adults according to background characteristics by sex, India, LASI Wave 1, 2017–18

Background characteristics Male Female Difference P-value
% %
Diabetes
 No 34.6 41.6 -7.0 0.001
 Yes 29.2 30.9 -1.6 0.001
Hypertension
 No 34.1 40.4 -6.3 0.001
 Yes 33.0 39.4 -6.4 0.001
Stroke
 No 33.6 40.0 -6.4 0.000
 Yes 39.7 41.5 -1.8 0.307
Heart Disease
 No 33.8 40.5 -6.7 0.001
 Yes 33.3 30.9 2.4 0.001
Age group (in years)
 Young-old (60–69) 28.9 36.5 -7.7 0.001
 Old-old (70–79) 38.4 44.7 -6.3 0.001
 Oldest-old (80 +) 47.8 47.4 0.4 0.290
Education
 No education 41.4 43.1 -1.8 0.001
 Primary 34.7 36.8 -2.1 0.001
 Secondary 26.2 23.5 2.7 0.758
 Higher 18.9 26.2 -7.3 0.103
Marital status
 Currently married 32.3 38.0 -5.7 0.001
 Widowed 38.6 41.8 -3.2 0.001
 Othersa 48.9 38.2 10.7 0.408
Working status
 Never worked 44.7 41.4 3.3 0.556
 Currently working 29.9 38.0 -8.1 0.001
 Not currently working 36.4 39.3 -3.0 0.001
Currently smoke tobacco
 No 33.9 40.0 -6.2 0.001
 Yes 33.5 39.6 -6.1 0.001
Currently chew tobacco
 No 33.2 40.0 -6.8 0.001
 Yes 35.4 40.2 -4.8 0.001
Alcohol consumption
 No 33.4 39.9 -6.5 0.001
 Yes 34.8 44.5 -9.7 0.001
MPCE quintile
 Poorest 38.2 42.0 -3.9 0.001
 Poorer 36.5 42.9 -6.5 0.001
 Middle 32.8 40.1 -7.4 0.001
 Richer 31.2 36.4 -5.3 0.001
 Richest 29.2 37.5 -8.3 0.001
Religion
 Hindu 33.6 40.1 -6.6 0.001
 Muslim 31.6 38.4 -6.8 0.001
 Christian 40.9 42.6 -1.7 0.001
 Othersb 40.4 40.8 -0.5 0.136
Caste
 Scheduled Caste 40.0 43.2 -3.2 0.001
 Scheduled Tribe 37.4 43.1 -5.6 0.001
 Other Backward Class 33.4 38.9 -5.6 0.001
 Others 29.0 37.9 -8.9 0.001
Place of residence
 Rural 36.3 42.6 -6.3 0.001
 Urban 26.8 34.2 -7.4 0.001
Region
 North 35.0 47.6 -12.6 0.001
 Central 34.4 39.3 -4.8 0.001
 East 37.2 43.6 -6.4 0.001
 Northeast 44.3 53.9 -9.6 0.001
 West 23.6 30.0 -6.3 0.001
 South 34.2 38.6 -4.3 0.001
Overall 33.8 40.0 -6.2 0.001

a Includes Divorced/Separated/Deserted/Others

b Includes Sikh, Buddhist/neo-Buddhist, Jain, Jewish, and Parsi/Zoroastrian; Differences: Male–Female

State-wise prevalence (%) of VI among older adults is presented in Fig. 1. Older males in Meghalaya (59.5%) had the highest prevalence of VI, followed by older males in Arunachal Pradesh (58.4%) and Tripura (45.2%). Additionally, older females in Arunachal Pradesh (77.4%) had the highest prevalence for VI, followed by Meghalaya (68.8%) and Delhi (56.1%). The state-wise prevalence of VI according to the 20/63 cut-off is provided in Fig. 1.

Fig. 1.

Fig. 1

Prevalence of VI among older adults in India and its states, 2017–18

Logistic regression estimates for VI among older adults is presented in Table 4. Diabetic patients significantly had 18% lower odds of having VI than that of non-diabetic individuals [AOR: 0.82; CI: 0.70, 0.95]. On the other hand, older who were suffering from hypertension and stroke had 12% [AOR: 1.12; CI: 1.01, 1.22] and 20% [AOR: 1.20; CI: 1.03, 1.53] higher likelihood of having VI than their counterparts.

Table 4.

Multivariable logistic regression estimates for VI among older adults, India, LASI Wave 1, 2017–18

Background characteristics AOR (CI)
Diabetes
 No 1.00
 Yes 0.82* (0.70,0.95)
Hypertension
 No 1.00
 Yes 1.12*(1.01,1.22)
Stroke
 No 1.00
 Yes 1.20*(1.03,1.53)
Heart Disease
 No 1.00
 Yes 0.90 (0.67,1.22)
Sex
 Male 1.00
 Female 0.98 (0.86,1.11)
Age group (in years)
 Young-old (60–69) 1.00
 Old-old (70–79) 1.39*** (1.24,1.54)
 Oldest-old (80 +) 1.58*** (1.32,1.89)
Education
 No education 1.00
 Primary 0.82*** (0.73,0.92)
 Secondary 0.53*** (0.43,0.64)
 Higher 0.42*** (0.34,0.52)
Marital status
 Currently married 1.00
 Widowed 1.01 (0.91,1.13)
 Othersa 1.42* (1.08,1.87)
Working status
 Never worked 1.00
 Currently working 0.77*** (0.67,0.88)
 Not currently working 0.89 (0.78, 1.01)
Currently smoke tobacco
 No 1.00
 Yes 0.83** (0.73,0.95)
Currently chew tobacco
 No 1.00
 Yes 0.97 (0.87,1.08)
Alcohol consumption
 No 1.00
 Yes 1.03 (0.91,1.16)
MPCE quintile
 Poorest 1.00
 Poorer 1.04 (0.92,1.18)
 Middle 0.93 (0.81,1.06)
 Richer 0.87 (0.75,1.00)
 Richest 0.89 (0.75,1.05)
Religion
 Hindu 1.00
 Muslim 0.85* (0.73,0.98)
 Christian 1.12 (0.90,1.39)
 Othersb 1.08 (0.89,1.33)
Caste
 Scheduled Caste 1.00
 Scheduled Tribe 0.94 (0.79,1.12)
 Other Backward Class 0.89 (0.79,1.00)
 Others 0.89 (0.78,1.01)
Place of residence
 Rural 1.00
 Urban 0.86* (0.76,0.98)
Region
 North 1.00
 Central 0.81** (0.71,0.92)
 East 0.92 (0.81,1.04)
 Northeast 1.34*** (1.14,1.57)
 West 0.55*** (0.48,0.64)
 South 0.86* (0.74,1.00)

a Includes Divorced/Separated/Deserted/Others

b Includes Sikh, Buddhist/neo-Buddhist, Jain, Jewish, and Parsi/Zoroastrian

p < 0.05*, p < 0.01**, p < 0.001***

Oldest old adults were 58% significantly more likely to suffer from VI than younger old adults [AOR: 1.58; CI: 1.32, 1.89]. Older adults with higher educational status had 58% significantly lower likelihood to suffer from VI than older adults with no education [AOR: 0.42; CI: 0.34, 0.52]. Separated/Divorced/Deserted/Others older adults had 42% significantly higher likelihood to suffer from VI than older adults who were currently married [AOR: 1.42; CI: 1.08, 1.87]. According to working status, currently working individuals had significantly lower odds of suffering from the VI than those who never worked [AOR: 0.77; CI: 0.67, 0.88]. It was found that higher the wealth quintile lowers the likelihood to suffer from lower vision problem among older adults. Older adults from urban place of residence had 14% significantly lower likelihood to suffer from VI than older adults from rural place of residence [AOR: 0.86; CI: 0.76, 0.98]. Older adults from northeast region had 34% significantly higher likelihood to suffer from VI than older adults from northern region [AOR: 1.34; CI: 1.14, 1.57]. The multivariable estimates according to the cut-point of worse than 20/63, are provided in Table S3.

Discussion

In this study, based on a large representative survey data, we examined the association of chronic diseases, socioeconomic factors and health behaviours with VI among older adults. The substantially higher prevalence of VI (37 percent) among older adults aged 60 and above, that in most cases can be avoided with early detection and timely intervention, calls for special attention from the health decision makers in the country. The prevalence rate with a female disadvantage is comparable with other studies in India [2629], and worldwide [4]. Moreover, the prevalence of blindness was 2.9% among Indian older adults which was lower than the prevalence (3.6%) reported in an earlier population-based survey of rapid assessment of avoidable blindness (RAAB) [30], and the pooled prevalence (4.17% for men and 5.68% for women) reported in a previous systematic review in India [31]. The variation in the prevalence of blindness in our study resulted from different method of assessment (we considered visual acuity of less than 3/60 in the better eye and being unable to count fingers or perceive light whereas, the systematic review also considered visual acuity < 6/60 in better eye, in the definition of blindness) and varied population age-group and time period. This variation can also be attributed to other socio-cultural and environmental and genetic factors [32] that are not considered in the current study.

Four major diseases related to VI were analysed and the prevalence of hypertension, and stroke were significantly positively associated with VI in our study. Hypertensive patients having higher odds of VI may be attributed to their improper compliance with medicines that leads to ophthalmic complications [33]. Hypertensive retinopathy is also a known complication that may also explain the current finding [34, 35]. Hypertension is reported as the most prevalent risk factor for stroke [36] which can also contribute to the increased risk of VI. Several previous studies have also examined VI as an index condition in conjunction with many of the chronic conditions [3739]. Our results were parallel to the findings of earlier studies showing post-stroke induced VI in older ages [4042]. Multiple studies have reported that older people with lowered vision and sensory impairments had increased risk for cardiovascular diseases and such diseases lie on the pathway from VI to mortality [4345]. Also, with regard to the relationship between vision-related problems and health outcomes, study found that 74.5 percent of older people with VI had co-occurrence of at least one of the chronic conditions [46, 47]. Similarly, higher prevalence of VI and blindness in multi-morbidity studies was highlighted in a systematic review of 41 geriatric studies [48], suggesting the possibility of reverse causality among the observed associations.

On the contrary, the prevalence of diabetes among older individuals was negatively associated with VI in our study which is at variance with previous studies showing a positive association of diabetes mellitus with VI and blindness [49, 50]. This unexpected finding may be explained by the fact that older adults who self-reported diagnosis of diabetes might have received routine medical care and eye exams and utilized vision enhancing interventions like eyeglasses and cataract surgery as well as were more likely to have proper compliance with medicine [51]. However, since diabetes is known to be an important cause of VI and blindness in India and across the globe [52], the current finding requires further investigation.

Furthermore, association of marital status as a social support typically found in epidemiological studies with VI suggests an increased risk for VI among elders who are divorced/ separated/ deserted or never married, which is also observed in previous studies [53]. For them, a scarcity of assistance may result from experiencing loss of vision that calls for a special attention to be paid. The results of the present study are also concomitant with previous studies on the association of increasing age with higher rate of vision-related problems and blindness [54]. Besides, consistent with a few studies in different parts of India, VI was highly prevalent among low socioeconomic strata and in poorest wealth quintile [29, 55]. The significant negative association of VI with educational status was also observed in earlier studies [56]. Information regarding accessibility and barriers to eye care services which is lacking in the current study might have helped to better understand the relatively higher odds of VI among the illiterate older adults.

Higher rates of VI among rural resident older people aged 60 years and above in our study was consistent with multiple studies in various parts of the country showing an urban–rural gradient of poor vision in older ages and higher prevalence in rural areas [30, 57, 58]. The significant rural–urban difference observed in this study can be attributed to more limited access to eye care services including cataract surgery in rural areas as compared to urban areas, which has been documented extensively in the literature [5961]. A community-based study in South India found that visual and hearing impairment are important health problems among older population in this region [62], suggesting a need for future studies with special focus on regional disparities in geriatric impairments including VI. Further, when looking at geographical differences, the increased prevalence of VI in northern and north-eastern regions are in variance with earlier studies in India showing more prevalence in southern and western regions of the country [27, 57]. Further studies with multi-level spatial analyses are warranted to explore the variations in visual impairment across regions and socioeconomic strata of older population in India.

Although the strengths of this study lie in its nationally representative sample of older adults aged 60 years and above and the use of measured prevalence of VI, several limitations are important to be acknowledged. All data regarding chronic conditions were based on respondents’ self- reports. Besides, causality cannot be established given the cross- sectional design. Moreover, reasons for vision-related problems should be explored separately for types of eye diseases using longitudinal and appropriate clinical studies.

Conclusion

The present analysis identified higher rates of VI among those who are diagnosed with hypertension or stroke, currently unmarried, socioeconomically poorer, less educated and urban resident older people that can inform strategies to engage high risk groups. The findings outline possibilities to update information that can be utilized in development and improvement of vision in an aging population. Also, it suggests that specific interventions that promote active aging are required for older individuals who are socioeconomically disadvantaged as well as visually impaired.

Supplementary Information

12886_2023_3009_MOESM1_ESM.docx (41.4KB, docx)

Additional file 1: Table S1. Age-sex adjusted and unadjusted prevalence of low vision among older adults in India, 2017–2018. Table S2. Prevalence (%) of VI among older adults according to background characteristics by sex, India, LASI Wave 1, 2017-18. Table S3. Multivariable logistic regression estimates for VI among older adults, India, LASI Wave 1, 2017-18.

Acknowledgements

Not applicable.

Abbreviations

VI

Vision impairment

AOR

Adjusted Odds Ratio

CI

Confidence Interval

MPCE

Monthly per capita expenditure

VIF

Variance inflation factor

Authors’ contributions

Conceived and designed the research paper: SS and TM; analysed the data: MK and SS; Contributed agents/materials/analysis tools: TM; Wrote the manuscript: TM and PD; Refined the manuscript: TM and MK. All authors read, reviewed and approved the final manuscript.

Funding

No funding was received for the study.

Availability of data and materials

The datasets generated and/or analysed during the current study are available in the Gateway to Global Aging Data, https://g2aging.org/.

Declarations

Ethics approval and consent to participate

Ethics approval was obtained from the Central Ethics Committee on Human Research (CECHR) under the Indian Council of Medical Research (ICMR) and the Institutional Review Boards of collaborating organizations including International Institute for Population Sciences (IIPS), Mumbai and the Ministry of Health and Family Welfare, Government of India. And all methods were carried out in accordance with the relevant guidelines and regulations of ICMR.

The survey agencies that conducted the field survey for the data collection have collected prior informed consent (signed and oral) for both the interviews and biomarker tests from the eligible respondents in accordance with Human Subjects Protection. In case of illiterate older people, informed consent was obtained from their legal guardians for the study participation.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Shobhit Srivastava, Email: shobhitsrivastava889@gmail.com.

Manish Kumar, Email: kumarmanishiips@gmail.com.

T. Muhammad, Email: muhammad.iips@gmail.com

Paramita Debnath, Email: paramitadebnath@iips.net.

References

  • 1.Beard JR, Officer A, De Carvalho IA, et al. The world report on ageing and health: a policy framework for healthy ageing. Lancet. 2016: Epub ahead of print. 10.1016/S0140-6736(15)00516-4. [DOI] [PMC free article] [PubMed]
  • 2.Pascolini D, Mariotti SP. Global estimates of visual impairment: 2010. Br J Ophthalmol. 2012:Epub ahead of print. 10.1136/bjophthalmol-2011-300539. [DOI] [PubMed]
  • 3.Bourne RRA, Flaxman SR, Braithwaite T, et al. Magnitude, temporal trends, and projections of the global prevalence of blindness and distance and near vision impairment: a systematic review and meta-analysis. Lancet Glob Health. 2017:Epub ahead of print. 10.1016/S2214-109X(17)30293-0. [DOI] [PubMed]
  • 4.Stevens GA, White RA, Flaxman SR, et al. Global prevalence of vision impairment and blindness: magnitude and temporal trends, 1990–2010. Ophthalmology. 2013;120:2377–2384. doi: 10.1016/j.ophtha.2013.05.025. [DOI] [PubMed] [Google Scholar]
  • 5.Dandona L, Dandona R. Revision of visual impairment definitions in the International Statistical Classification of Disease. BMC Med. 2006:Epub ahead of print. 10.1186/1741-7015-4-7. [DOI] [PMC free article] [PubMed]
  • 6.National Academies of Sciences Engineering and Medicine . Making eye health a population health imperative: vision for tomorrow. 2016. The impact of vision loss. [PubMed] [Google Scholar]
  • 7.Salvi SM, Akhtar S, Currie Z. Ageing changes in the eye. Postgrad Med J. 2006:Epub ahead of print. 10.1136/pgmj.2005.040857. [DOI] [PMC free article] [PubMed]
  • 8.Whillans J, Nazroo J. Social inequality and visual impairment in older people. J Gerontol Ser B Psychol Sci Soc Sci. 2018:Epub ahead of print. 10.1093/geronb/gbv163. [DOI] [PubMed]
  • 9.Swenor BK, Lee MJ, Varadaraj V, et al. Aging with vision loss: a framework for assessing the impact of visual impairment on older adults. Gerontologist. 2020;60:989–995. doi: 10.1093/geront/gnz117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Court H, McLean G, Guthrie B, et al. Visual impairment is associated with physical and mental comorbidities in older adults: a cross-sectional study. BMC Med. 2014:Epub ahead of print. 10.1186/s12916-014-0181-7. [DOI] [PMC free article] [PubMed]
  • 11.Wang WL, Chen N, Sheu MM, et al. The prevalence and risk factors of visual impairment among the elderly in Eastern Taiwan. Kaohsiung J Med Sci. 2016:Epub ahead of print. 10.1016/j.kjms.2016.07.009. [DOI] [PMC free article] [PubMed]
  • 12.Guo C, Wang Z, He P, et al. Prevalence, causes and social factors of visual impairment among Chinese adults: based on a national survey. Int J Environ Res Public Health. 2017:Epub ahead of print. 10.3390/ijerph14091034. [DOI] [PMC free article] [PubMed]
  • 13.Evans JR, Fletcher AE, Wormald RPL, et al. Prevalence of visual impairment in people aged 75 years and older in Britain: results from the MRC trial of assessment and management of older people in the community. Br J Ophthalmol. 2002;86:795–800. doi: 10.1136/bjo.86.7.795. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Carabellese C, Appollonio I, Rozzini R, et al. Sensory impairment and quality of life in a community elderly population. J Am Geriatr Soc. 1993:Epub ahead of print. 10.1111/j.1532-5415.1993.tb06948.x. [DOI] [PubMed]
  • 15.The Longitudinal Ageing Study in India 2017-18 - national report. International Institute for Population Sciences. National Programme for Health Care of Elderly, Ministry of Health and Family Welfare, Harvard T. H. Chan School of Public Health, and the University of Southern California. 2020.
  • 16.National Research Council . Visual impairments: determining eligibility for social security benefits. Washington (DC): National Academies Press; 2002. Committee on future directions for cognitive research. [PubMed] [Google Scholar]
  • 17.Islam S, Upadhyay AK, Mohanty SK, et al. Use of unclean cooking fuels and visual impairment of older adults in India: a nationally representative population-based study. Environ Int. 2022;165:107302. doi: 10.1016/j.envint.2022.107302. [DOI] [PubMed] [Google Scholar]
  • 18.McKenna SP. Measuring patient-reported outcomes: moving beyond misplaced common sense to hard science. BMC Med. 2011:Epub ahead of print. 10.1186/1741-7015-9-86. [DOI] [PMC free article] [PubMed]
  • 19.Srivastava S, Muhammad T. Violence and associated health outcomes among older adults in India: a gendered perspective. SSM Popul Health. 2020;12:Epub ahead of print 1 December. 10.1016/j.ssmph.2020.100702. [DOI] [PMC free article] [PubMed]
  • 20.Zacharias A, Vakulabharanam V. Caste Stratification and wealth inequality in India. World Dev. 2011:Epub ahead of print. 10.1016/j.worlddev.2011.04.026.
  • 21.Cohen J. Statistical power analysis for the behavioral sciences. 1977. The test that a proportion is .50 and the sign test. [Google Scholar]
  • 22.King J. (Ed). Binary logistic regression. SAGE Publications, Inc. 2008. 10.4135/9781412995627.
  • 23.StataCorp . Stata: release 14. Statistical software. 2015. [Google Scholar]
  • 24.Lewis-Beck M, Bryman A, Futing Liao T. The SAGE encyclopedia of social science research methods. 2012. Variance inflation factors. [Google Scholar]
  • 25.Vogt W. Dictionary of statistics & methodology. 2015. Variance Inflation Factor (VIF) [Google Scholar]
  • 26.Nangia V, Jonas JB, Gupta R, et al. Visual impairment and blindness in rural central India: the Central India Eye and Medical Study. Acta Ophthalmol (Copenh) 2013;91:483–486. doi: 10.1111/j.1755-3768.2012.02447.x. [DOI] [PubMed] [Google Scholar]
  • 27.Marmamula S, Narsaiah S, Shekhar K, et al. Visual impairment in the South Indian State of Andhra Pradesh: Andhra Pradesh - Rapid Assessment of Visual Impairment (AP-RAVI) Project. PLoS One. 2013;8:Epub ahead of print. 10.1371/journal.pone.0070120. [DOI] [PMC free article] [PubMed]
  • 28.Vijaya L, George R, Asokan R, et al. Prevalence and causes of low vision and blindness in an urban population: the Chennai glaucoma study. Indian J Ophthalmol. 2014;62:477–481. doi: 10.4103/0301-4738.111186. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Mactaggart I, Polack S, Murthy GVS, et al. A population-based survey of visual impairment and its correlates in Mahabubnagar district, Telangana State. India Ophthalmic Epidemiol. 2018;25:238–245. doi: 10.1080/09286586.2017.1418386. [DOI] [PubMed] [Google Scholar]
  • 30.Neena J, Rachel J, Praveen V, et al. Rapid assessment of avoidable blindness in India. PLoS ONE. 2008;3:1–7. doi: 10.1371/journal.pone.0002867. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Prasad M, Malhotra S, Kalaivani M, et al. Gender differences in blindness, cataract blindness and cataract surgical coverage in India: a systematic review and meta-analysis. Br J Ophthalmol. 2020;104:220–224. doi: 10.1136/bjophthalmol-2018-313562. [DOI] [PubMed] [Google Scholar]
  • 32.Lavanya R, Jeganathan VSE, Zheng Y, et al. Methodology of the Singapore Indian Chinese Cohort (SICC) eye study: quantifying ethnic variations in the epidemiology of eye diseases in Asians. Ophthalmic Epidemiol. 2009;16:325–336. doi: 10.3109/09286580903144738. [DOI] [PubMed] [Google Scholar]
  • 33.Gazzard G, Konstantakopoulou E, Garway-Heath D, et al. Selective laser trabeculoplasty versus eye drops for first-line treatment of ocular hypertension and glaucoma (LiGHT): a multicentre randomised controlled trial. Lancet. 2019;393:1505–1516. doi: 10.1016/S0140-6736(18)32213-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Bhargava M, Ikram MK, Wong TY. How does hypertension affect your eyes? J Hum Hypertens. 2012;26:71–83. doi: 10.1038/jhh.2011.37. [DOI] [PubMed] [Google Scholar]
  • 35.Wong T, Mitchell P. The eye in hypertension. Lancet. 2007;369:425–435. doi: 10.1016/S0140-6736(07)60198-6. [DOI] [PubMed] [Google Scholar]
  • 36.Wajngarten M, Silva GS. Hypertension and stroke: update on treatment. Eur Cardiol Rev. 2019;14:111. doi: 10.15420/ecr.2019.11.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Adelson JD, Bourne RRA, Briant PS, et al. Causes of blindness and vision impairment in 2020 and trends over 30 years, and prevalence of avoidable blindness in relation to VISION 2020: the right to sight: an analysis for the Global Burden of Disease Study. Lancet Glob Health 2020:Epub ahead of print. 10.1016/s2214-109x(20)30489-7. [DOI] [PMC free article] [PubMed]
  • 38.Bourne RRA, Stevens GA, White RA, et al. Causes of vision loss worldwide, 1990–2010: a systematic analysis. Lancet Glob Health. 2013;1:339–349. doi: 10.1016/S2214-109X(13)70113-X. [DOI] [PubMed] [Google Scholar]
  • 39.Park SJ, Ahn S, Park KH. Burden of visual impairment and chronic diseases. JAMA Ophthalmol. 2016;134:778–784. doi: 10.1001/jamaophthalmol.2016.1158. [DOI] [PubMed] [Google Scholar]
  • 40.Sand KM, Midelfart A, Thomassen L, et al. Visual impairment in stroke patients - a review. Acta Neurol Scand. 2013;127:52–56. doi: 10.1111/ane.12050. [DOI] [PubMed] [Google Scholar]
  • 41.Sand KM, Wilhelmsen G, Næss H, et al. Vision problems in ischaemic stroke patients: effects on life quality and disability. Eur J Neurol. 2016;23:1–7. doi: 10.1111/ene.12848. [DOI] [PubMed] [Google Scholar]
  • 42.Khairallah M, Kahloun R, Bourne R, et al. Number of people blind or visually impaired by cataract worldwide and in world regions, 1990 to 2010. Invest Ophthalmol Vis Sci. 2015;56:6762–6769. doi: 10.1167/iovs.15-17201. [DOI] [PubMed] [Google Scholar]
  • 43.Kulmala J, Era P, Törmäkangas T, et al. Visual acuity and mortality in older people and factors on the pathway. Ophthalmic Epidemiol. 2008;15:128–134. doi: 10.1080/09286580701840388. [DOI] [PubMed] [Google Scholar]
  • 44.Buddeke J, Bots ML, Van Dis I, et al. Comorbidity in patients with cardiovascular disease in primary care: a cohort study with routine healthcare data. Br J Gen Pract. 2019;69:E398–E406. doi: 10.3399/bjgp19X702725. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Liljas AEM, Wannamethee SG, Whincup PH, et al. Sensory impairments and cardiovascular disease incidence and mortality in older British community-dwelling men: a 10-year follow-up study. J Am Geriatr Soc. 2016;64:442–444. doi: 10.1111/jgs.13975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Zheng DD, Christ SL, Lam BL, et al. Visual acuity and increased mortality: the role of allostatic load and functional status. Invest Ophthalmol Vis Sci. 2014;55:5144–5150. doi: 10.1167/iovs.14-14202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Jones GC, Rovner BW, Crews JE, et al. Effects of depressive symptoms on health behavior practices among older adults with vision loss. Rehabil Psychol. 2009;54:164–172. doi: 10.1037/a0015910. [DOI] [PubMed] [Google Scholar]
  • 48.Marengoni A, Angleman S, Melis R, et al. Aging with multimorbidity: a systematic review of the literature. Ageing Res Rev. 2011;10:430–439. doi: 10.1016/j.arr.2011.03.003. [DOI] [PubMed] [Google Scholar]
  • 49.Cui Y, Zhang L, Zhang M, et al. Prevalence and causes of low vision and blindness in a Chinese population with type 2 diabetes: the Dongguan Eye Study. Sci Rep. 2017;7:1–9. doi: 10.1038/s41598-017-11365-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Idil A, Caliskan D, Ocaktan E. The prevalence of blindness and low vision in older onset diabetes mellitus and associated factors: a community-based study. Eur J Ophthalmol. 2004;14:298–305. doi: 10.1177/112067210401400404. [DOI] [PubMed] [Google Scholar]
  • 51.Ehrlich JR, Ndukwe T, Chien S, et al. The association of cognitive and visual function in a nationally representative study of older adults in India. Neuroepidemiology. 2021;55:126–134. doi: 10.1159/000513813. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Gadkari SS, Maskati QB, Nayak BK. Prevalence of diabetic retinopathy in India: the all India ophthalmological society diabetic retinopathy eye screening study 2014. Indian J Ophthalmol. 2016;64:38. doi: 10.4103/0301-4738.178144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Horowitz A, Brennan M, Reinhardt JP. Prevalence and risk factors for self-reported visual impairment among middle-aged and older adults. Res Aging. 2005;27:307–326. doi: 10.1177/0164027504274267. [DOI] [Google Scholar]
  • 54.Limburg H, Von-Bischhoffshausen FB, Gomez P, et al. Review of recent surveys on blindness and visual impairment in Latin America. Br J Ophthalmol. 2008;92:315–319. doi: 10.1136/bjo.2007.125906. [DOI] [PubMed] [Google Scholar]
  • 55.Avachat S, Phalke V, Kambale S. Epidemiological correlates of cataract cases in tertiary health care center in rural area of Maharashtra. J Fam Med Prim Care. 2014;3:45. doi: 10.4103/2249-4863.130273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Zhao J, Xu X, Ellwein LB, et al. Prevalence of vision impairment in older adults in rural China in 2014 and comparisons with the 2006 China Nine-Province Survey. Am J Ophthalmol. 2018;185:81–93. doi: 10.1016/j.ajo.2017.10.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Patil S, Gogate P, Vora S, et al. Prevalence, causes of blindness, visual impairment and cataract surgical services in Sindhudurg district on the western coastal strip of India. Indian J Ophthalmol. 2014;62:240–245. doi: 10.4103/0301-4738.128633. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Singh N, Eeda SS, Gudapati BK, et al. Prevalence and causes of blindness and visual impairment and their associated risk factors, in three tribal areas of Andhra Pradesh, India. PLoS ONE. 2014;9:3–10. doi: 10.1371/journal.pone.0100644. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Gilbert CE, Shah SP, Jadoon MZ, et al. Poverty and blindness in Pakistan: results from the Pakistan national blindness and visual impairment survey. BMJ. 2008;336:29–32. doi: 10.1136/bmj.39395.500046.AE. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 60.He M, Abdou A, Naidoo KS, et al. Prevalence and correction of near vision impairment at seven sites in China, India, Nepal, Niger, South Africa, and the United States. Am J Ophthalmol. 2012;154:107–116.e1. doi: 10.1016/j.ajo.2012.01.026. [DOI] [PubMed] [Google Scholar]
  • 61.Malhotra S, Vashist P, Kalaivani M, et al. Prevalence and causes of visual impairment amongst older adults in a rural area of North India: a cross-sectional study. BMJ Open. 2018;8:e018894. doi: 10.1136/bmjopen-2017-018894. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Deepthi R, Kasthuri A. Visual and hearing impairment among rural elderly of south India: a community-based study. Geriatr Gerontol Int. 2012;12:116–122. doi: 10.1111/j.1447-0594.2011.00720.x. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

12886_2023_3009_MOESM1_ESM.docx (41.4KB, docx)

Additional file 1: Table S1. Age-sex adjusted and unadjusted prevalence of low vision among older adults in India, 2017–2018. Table S2. Prevalence (%) of VI among older adults according to background characteristics by sex, India, LASI Wave 1, 2017-18. Table S3. Multivariable logistic regression estimates for VI among older adults, India, LASI Wave 1, 2017-18.

Data Availability Statement

The datasets generated and/or analysed during the current study are available in the Gateway to Global Aging Data, https://g2aging.org/.


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