There are currently an estimated 50 million people with dementia worldwide, with this expected to rise to 152.8 million by 2050.1 The growth in numbers of people with dementia is largely driven by increasing life expectancy in low- and middle-income countries (LMICs). However, many LMICs lack basic national prevalence data on dementia, and so are reliant on estimates based on regional statistical modelling, as used within the Global Burden of Disease study.1 These estimates, although useful for their global coverage, are limited by the robustness of the model and the availability of country-specific data. They are also less powerful than local data in making the case for national policy priority. The Strengthening Responses to Dementia in Developing Countries (STRiDE) programme identified that policy makers and key stakeholders wanted robust national estimates of dementia prevalence, and that there was a reluctance to act on data derived even from geographically close or socioeconomically similar settings.Reference Breuer, Comas-Herrera, Freeman, Albanese, Alladi and Amour2 In two STRiDE countries, South Africa and Indonesia, local prevalence data were identified as a priority need.Reference Farina, Jacobs and Sani3
In South Africa, there are few studies that explore dementia prevalence. The single best evidence comes from 1394 Xhosa-speaking older adults in Cape Town.Reference de Jager, Msemburi, Pepper and Combrinck4 The study used a dementia screening tool, the Brief Community Screening Instrument for Dementia (CSI-D),Reference Prince, Acosta and Ferri5 and estimated dementia prevalence to be 11% for those aged 65 years and older.Reference de Jager, Msemburi, Pepper and Combrinck4 Other estimates of dementia prevalence come from studies with small sample sizes and potentially non-representative samples.Reference Ben-Arie, Swartz, Teggin and Elk6 Evidence on dementia prevalence from Indonesia is geographically limited to the islands of Java and Bali.Reference Hogervorst, Mursjid, Ismail and Jacobsen7–Reference Suriastini, Turana, Supraptilah, Wicaksono and Mulyanto9 Excluding issues of generalisability, these studies have often reported unusually high prevalence estimates (>20%) compared with many international estimates (e.g. 4–9%, aged 60 years and older).Reference Prince, Wimo, Guerchet, Ali, Wu and Prina10
Aims
STRiDE aimed to develop and deliver a pragmatic methodology to generate accurate dementia prevalence estimates in LMICs, sampling from rural and urban areas, using South Africa and Indonesia as exemplars. This methodology seeks to improve on existing evidence by minimising internal and external bias, and simultaneously generating data to measure both the impact and cost of dementia in these two settings, and with appropriate cultural adaptation in other LMICs.
Method
The STRiDE programme developed a common data collection approach with the capacity for methods to vary pragmatically to access and use existing sampling frames.
Participants
Recruitment occurred in two sites in each country: Jakarta and North Sumatra in Indonesia, and Limpopo and Western Cape in South Africa. Sites were selected for pragmatic reasons and to ensure heterogeneity in terms of socioeconomic status and rurality. Random sampling was used: simple randomisation in Limpopo and proportionate to population size randomisation in other sites. Details of sites and sampling strategy are shown in Supplementary Appendix 1, available at https://doi.org/10.1192/bjo.2023.76.
To be eligible, participants were required to be aged 65 years or older at the date of consent, speak one of the languages of the adapted toolkits (Afrikaans, Bahasa Indonesian, English, isiXhosa, Sepedi) and live within the defined sampling areas. We checked the age of participants informally before consent and more rigorously following consent (e.g. from official documents and using the calendar method). All participants were required to identify an informant who could provide supplementary information. The informant could be anyone with a close relationship with the older adult and who spoke the appropriate language. Potential participants were excluded if they resided in care or nursing homes, or they lacked capacity to consent and could not identify a personal consultee to assist in the consent process.
Procedure
Researchers visited potential participants’ homes (or another location convenient to participants) in pairs. Informed consent was obtained (written or oral) from the older adult and an identified informant. Researchers initially completed a core set of questions related to age and household with both the informant and older adult. Subsequently, the older adult and informant completed the remaining questionnaires independently of each other, one with each of the researchers. Measures pertaining to the identification of dementia (as described below) were prioritised. In a single-stage process, all participants were asked the same set of questions, with the exception of some branching (e.g. care-related questions were skipped if no care was provided). Study data were collected and managed with REDCap electronic data capture tools (REDCap Consortium, Vanderbilt University, Nashville, TN, USA; https://projectredcap.org/) hosted at the London School of Economics and Political Sciences.Reference Harris, Taylor, Thielke, Payne, Gonzalez and Conde11
All researchers were provided standardised training in how to administer the questionnaires before testing. We developed a series of presentations and standard operating procedures centrally to guide researchers. Data collection occurred between September 2021 and December 2021.
Measures
A series of demographic measures were collected, including age (ascertained through a hierarchy of self-report, informant report, official documentation and the calendar method), sex, literacy (ability to read and write) and self-report receipt of a diagnosis of dementia or Alzheimer's disease. The following instruments were completed: 10/66 short schedule, Dementia Severity Rating Scale (DSRS) and Lawton Activities of Daily Living Scale.
The 10/66 Short Dementia Diagnostic ScheduleReference Stewart, Guerchet and Prince12 is composed of the following measures: (a) the CSI-D, a screening instrument for dementia for use in cross-cultural studies,Reference Hall, Gao, Emsley, Ogunniyi, Morgan and Hendrie13 with both a cognitive assessment component and an informant-reported functional impairment component; (b) the EURO-D, a self-report measure to screen for depression;Reference Prince, Reischies and Beekman14 and (c) the Consortium to Establish a Registry for Alzheimer's Disease (CERAD), a ten-word list learning task with delayed recall.Reference Morris, Heyman and Mohs15 We used the 10/66 short algorithm to generate an estimate of dementia caseness,Reference Stewart, Guerchet and Prince12 which uses data derived from the CSI-D, CERAD word list and EURO-D (Supplementary Appendix 2). The 10/66 short algorithm has been demonstrated to have good sensitivity across multiple settings,Reference Stewart, Guerchet and Prince12 including against clinical diagnosis in Singapore (area under the curve (AUC) = 0.87),Reference Abdin, Vaingankar and Picco16 Switzerland (AUC = 0.74)Reference Ibnidris, Piumatti and Carlevaro17 and Pakistan (AUC = 0.85).Reference Khan and Prince18
The DSRS is a brief informant report measure of 12 functional abilities similar to those in the Clinical Dementia Rating (CDR) scale.Reference Clark and Ewbank19 The DSRS predicts the CDR sum of boxes score.Reference Moelter, Glenn and Xie20 Scores range from 0 to 54, with higher scores representing greater impairment. The measure was completed as an informant report measure.
The Lawton Activities of Daily Living Scale is a short questionnaire that covers eight instrumental activities of daily living.Reference Lawton and Brody21 The measure was completed as an informant report measure.
Measures of cost and impact were also completed, but these did not contribute to the dementia prevalence calculations and are not reported here. Indonesian participants were interviewed in Bahasa Indonesian, and South Africa participants were interviewed in isiXhosa, Sepedi, Afrikaans or English. Details of the full STRiDE toolkit and the underlying cross-cultural adaptation and translation process are described elsewhere.Reference Farina, Jacobs and Sani3
Ethics
The authors assert that all procedures contributing to this work comply with the ethical standards of the relevant national and institutional committees on human experimentation and with the Helsinki Declaration of 1975, as revised in 2008. All procedures involving human patients were approved by the London School of Economics and Political Sciences, University of Cape Town, University of Sumatera Utara (approval number 862/KEP/USU/2020) and Atma Jaya Catholic University (approval number 01/12/KEP-FKIKUAJ/2020).
Sample size calculation
Precision calculations indicated that an overall sample of 2039 would allow the estimation of an expected dementia prevalence of 4.5% with a precision of ±0.9% within each country. The recruitment target was increased to 2200 to allow for missing data.
Analysis
Demographic data were generated separately for each country; we present key demographics for dementia occurrence and assessment (age in 5-year intervals, sex, literacy), in line with previous dementia prevalence research.Reference Chandra, Ganguli, Pandav, Johnston, Belle and DeKosky22 We investigated representativeness of the study sample in a series of Pearson's chi-squared analyses, which were used to ascertain whether demographic factors differed between those with complete or missing data (i.e. those for which we had sufficient data to run the diagnostic algorithm).
We calculated total prevalence (10/66 short algorithm) estimates unweighted, with 95% confidence intervals. We then weighted data by national demography (age, sex and literacy), and computed national proportions from Indonesia and from South Africa. We generated weights based on sequential computation (Supplementary Appendix 3).
Next, we ran logistic regression models to explore factors potentially associated with increased risk of dementia, and subsequently calculated age-adjusted odds ratios for sex and literacy. We also ran supplementary Poisson regression models to generate prevalence ratios. We explored convergent validity of the 10/66 short algorithm against cognitive impairment (Brief CSI-D screening tool cognitive scale), functional impairment (Brief CSI-D screening tool informant scale, Lawton Activities of Daily Living scale) and care needs (older adult needs care, yes/no), reporting the effect size between populations (Hedges’ g). For Hedges’ g, a value >0.5 indicates a medium effect size, and a value >0.8 indicates a large effect size. In addition, participants who scored positive for dementia on the 10/66 short algorithm were compared against existing cut-offs of dementia on the DSRS and the Brief CSI-D (Supplementary Appendix 4). For these comparisons, we calculated the AUC ((sensitivity + specificity)/2) between measures. We interpreted the AUC according to existing criteria: a score of 0.5–0.6 is considered poor accuracy, 0.6–0.7 is considered acceptable accuracy, 0.7–0.8 is considered good accuracy and >0.8 is considered very good or excellent accuracy.Reference Šimundić23
Results
See Fig. 1 for a flow diagram of participant recruitment. In Indonesia, we recruited to target; in South Africa, we adhered to the planned recruitment strategy and procedures, but we were unable to reach the target sample size because of disruptions caused by the COVID-19 pandemic.
Fig. 1 Participant recruitment flow diagram within each site, for September to December 2021. The 10/66 short schedule refers to the 10/66 Short Dementia Diagnostic Schedule. DIMAMO, Dikgale, Mamabolo and Mothiba; DKI, Daerah Khusus Ibukota.
Missing data
In Indonesia, we recruited 2216 participants. In South Africa, we recruited 490 participants. Across sites, there were instances in which only partial data were available because of participant refusal, or researcher or technical error. In the Indonesian cohort, there were 106 participants (4.8%) with insufficient data to run the 10/66 short algorithm. Missing data were not associated with age (n = 2216, χ 2 = 2.64, P = 0.76), literacy (n = 2173, χ 2 = 0.37, P = 0.54) or sex (n = 2216, χ 2 = 0.88, P = 0.35). In the South African cohort, there were 82 participants (16.7%) for whom we were unable to run the 10/66 short algorithm, predominantly because of refusal to answer the EURO-D (n = 64). Ability to run the algorithm was not associated with age (n = 489, χ 2 = 4.04, P = 0.54), literacy (n = 470, χ 2 = 0.33, P = 0.56) or sex (n = 467, χ 2 = 0.01, P = 0.92).
Demographics
Dementia prevalence was estimated in 2110 older adults in Indonesia and 408 older adults in South Africa. Mean age of participants was 71.1 (s.d. = 5.42) years in Indonesia and 74.8 (s.d. = 7.42) years in South Africa. Both country samples contained higher proportions of women than men (up to 63.5% in South Africa) (Table 1). Men were 2.50 times more likely to be literate in Indonesia than women (Mantel–Haenszel χ 2 = 49.66, P < 0.001). Men were 1.73 times more likely to be literate in South Africa than women (Mantel–Haenszel χ 2 = 4.71, P = 0.03). See Supplementary Appendix 5 for the number of participants by country, age, sex and literacy.
Table 1 Summary of key demographic variables, split by country
Only five participants (0.2%) in Indonesia and two (0.5%) participants in South Africa had been previously diagnosed with dementia.
Prevalence
Unweighted estimates of dementia for those aged 65 years and older were 26.6% (95% CI 24.8–28.6) in Indonesia and 14.5% (95% CI 11.2–18.3) in South Africa. After national weighting, estimates marginally increased to 27.9% (95% CI 25.2–28.9) in Indonesia and decreased to 12.5% (95% CI 9.5–16.0) in South Africa. Unweighted prevalence estimates by country, age, sex and literacy are reported in Table 2.
Table 2 Prevalence estimates split by age, sex and literacy, using the 10/66 short-form algorithm (grand total prevalence is also reported in both weighted and unweighted formats)
The 10/66 short-form refers to the 10/66 Short Dementia Diagnostic Schedule.
a. Grand total may be higher than subgroups because of missing demographic details.
b. Weighted by national age, sex and literacy estimates; see Supplementary Appendix 3 for weightings.
Associations with dementia
Across both countries, dementia increased with age and decreased in literate compared with illiterate participants. Dementia prevalence was lower in men compared with women in Indonesia, but no such association was found in South Africa. After adjusting for age, the associations remained largely unchanged in Indonesia, although illiteracy was no longer associated with dementia prevalence in South Africa (Table 3). Similar findings were found when calculating prevalence ratios (Supplementary Appendix 6).
Table 3 Odds of dementia against age, sex and literacy in Indonesia and South Africa
a. Age compared with 65–69 year category.
b. Male compared with female category.
c. Literacy compared with illiterate category (unable to read or write).
Concurrent validity
In both countries, the 10/66 short algorithm was able to differentiate scores based on the Brief CSI-D cognitive score, Brief CSI-D screening tool informant score, DSRS, Lawton Activities of Daily Living Scale and need for care (P < 0.001). All outcome variables had a large effect size between dementia positive and negative cases, with the exception of the need for care in Indonesia (Hedges' g = 0.70). The 10/66 short algorithm demonstrated good accuracy in Indonesia (AUC = 0.75, 95% CI 0.72–0.77) and very good accuracy in South Africa (AUC = 0.82, 95% CI = 0.76–0.88) against the DSRS screening cut-off. Similarly, the 10/66 algorithm demonstrated good accuracy in Indonesia (AUC = 0.79, 95% CI 0.76–0.81) and very good accuracy in South Africa (AUC = 0.80, 95% CI 0.73–0.87) against the Brief CSI-D screening tool (Supplementary Appendix 4).
Discussion
This paper presents data on dementia prevalence from the STRiDE programme, serving as a proof of concept and validation of the STRiDE method for use in further studies in other LMICs. The data reported here applies standard methods, and contributes new, directly comparable, good-quality empirical data to the sparse dementia prevalence literature in two populous and culturally diverse middle-income countries, Indonesia and South Africa. This study is the first to generate prevalence data derived from the rural regions of North Sumatra (Indonesia) and Limpopo (South Africa). The findings indicate dementia prevalence estimates that are higher than those usually generated internationally, markedly so in the case of Indonesia. Our weighted prevalence estimates indicate that there may be 4 297 000 people with dementia in Indonesia and 450 000 people with dementia in South Africa (populations of people aged 65 years and older derived from 2018 estimates in Indonesia and 2020 estimates in South Africa; Supplementary Appendix 3). Our estimates exceed the numbers generated through modelling in the Global Burden of Disease 2019 study in Indonesia (768 000; 95% uncertainty interval 656 000–895 000) and South Africa (208 000; 95% uncertainty interval 179 000–241 000).1 The very low level of diagnosis of dementia in both countries is striking, with <1% of each sample reporting that they had received a diagnosis. Without diagnosis there is no chance of effective care and treatment for the person with dementia or support for their family carers. The results of this study illustrate the size of the challenge facing many countries and the importance of prioritising dementia at a policy level.
Although the estimates of dementia prevalence reported here look high, they may not be incorrect. The weighted dementia prevalence estimate for those aged 65 years and older in South Africa (12.5%) is in line with a previous study among isiXhosa speakers in Cape Town, which used the Brief CSI-D screening tool to identify cases (11%; 95% CI 9–13).Reference de Jager, Msemburi, Pepper and Combrinck4 Similarly, our prevalence estimate in Indonesia (27.9%) is in line with a growing evidence base across geographic regions in the country, albeit in those aged 60 years and older: Borobudur (15.9%),Reference Ben-Arie, Swartz, Teggin and Elk6 Yogyakarta (20.1%)Reference Ong, Annisafitrie and Purnamasari8 and Jatinangor (29.2%).Reference Hogervorst, Mursjid, Ismail and Jacobsen7 Some Indonesian studies have reported lower prevalence rates in certain settings: for example, dementia prevalence in Jakarta was estimated to be 4.5%,Reference Ben-Arie, Swartz, Teggin and Elk6 but the methodology in all of these studies is suboptimal and all previous studies used non-clinical diagnostic criteria or brief screening tools, which may introduce different and unquantified measurement bias than reported here (e.g. not accounting for depression as a comorbidity). The 10/66 Short Dementia Diagnostic Schedule does not require administration by clinicians and so has value in estimating prevalence in LMICs, not least because it is a more affordable strategy and does not require specialists to be diverted away from their clinical practice. Its validity has been extensively demonstrated across cultures and diverse settings.Reference Stewart, Guerchet and Prince12,Reference Abdin, Vaingankar and Picco16–Reference Khan and Prince18
There are a number of potential explanations for the high prevalence rates found in this study compared with regional World Health Organization estimates. First, the 10/66 short algorithm generates variability in prevalence estimates depending on country, from 3.4% in rural China to 13.0% in the Dominican Republic.Reference Stewart, Guerchet and Prince12 This country-specific variability is not dissimilar to the standard algorithm, but at present it does not appear that the short algorithm systematically overestimates prevalence compared with the standard algorithm. However, as with the standard algorithm,Reference Prince, Acosta, Chiu, Scazufca and Varghese24 elevated prevalence may represent higher sensitivity enabling the detection of milder cases rather than generating false positives. Second, there is the question of education fairness. The 10/66 short schedule was developed to be more education-fair than DSM criteria,Reference Prince, Acosta, Chiu, Scazufca and Varghese24 but reports have suggested the false positive rate of the 10/66 short algorithm in low education groups may be 5.5%.Reference Khan and Prince18 However, the exclusion of the illiterate subgroup from our analysis still yields prevalence rates higher than other international estimates of dementia. Third, the elevated prevalence could be real and explained by differences in risk factors in the populations studied. The comparatively higher prevalence in Indonesia could be driven, in part, by these population-level risk factors. For example, although Indonesia and South Africa both have a high cardiovascular disease burden,Reference Chow, Atkins, Shariful Islam and Lung25,Reference Byrne, Eksteen and Crickmore26 Indonesia has a higher prevalence of cerebrovascular disease.Reference Roth, Johnson and Abajobir27 Selection bias and measurement error seem unlikely given our sampling and the fact that we rigorously translated and cross-culturally adapted the schedule,Reference Farina, Jacobs and Sani3 in addition to implementing robust, standardised procedures for data collection and management, including the training and close supervision of all researchers.
Our observed associations between dementia prevalence and sex, age and literacy are in line with previous evidence, which provides some validation of our findings. Both countries demonstrated the expected age-related trend: older subgroups had greater likelihood of having dementia compared with younger subgroups. As expected, literacy was protective of the likelihood of dementia in both countries, although the findings become non-significant after controlling for age in South Africa. The association between literacy and dementia prevalence can be explained in terms of cognitive reserve,Reference Prince, Acosta and Ferri28 with education increasing a person's cognitive reserve, thus delaying the clinical onset of the condition. Men were found to have reduced likelihood of dementia compared with women in Indonesia, but not in South Africa. Men are often reported to have a lower prevalence of dementia compared with women,Reference Eastman, Bahorik, Kornblith, Xia and Yaffe29 which can be attributed to higher mortality, even within age groups, resulting from an accumulation of risk factors, such as increased risk of depression and cardiovascular disease.Reference Li and Singh30 The fact that women were more likely to be illiterate than men in both countries provides additional complexity. If cognitive reserve is protective of dementia onset, this might demonstrate an important inequality that needs to be addressed, given that education increases cognitive reserve. Such late-life disadvantage in cognitive health in women as a result of inequality earlier in life has also been noted in other LMICs such as India.Reference Angrisani, Jain and Lee31
Strengths of our study include the use of a standardised toolkit and methodologies across two middle-income countries, harmonised in terms of outcome measures and derived using a good-quality, cross-cultural adaptation process. There are, however, important limitations to consider. First, data from South Africa must be considered as preliminary, as the sample is insufficiently powered and results in wide confidence intervals. The COVID-19 pandemic limited recruitment in South Africa, but the data are a proof of concept and allow for the design and delivery of a more definitive study. Anecdotally, the pandemic may also have led to selection bias owing to potentially vulnerable older adults being wary of face-to-face contact, even in the absence of governmental restrictions. Second, the sampling strategy was pragmatic and attempted to capture both rural and urban regions within each country. Although weighted prevalence estimates were calculated according to the national demographic profiles to improve generalisability, it is important to acknowledge that the heterogeneous nature of both countries’ populations increases the uncertainty of these estimates on a national level. The method could be used in other regions to generate more representative estimates at local and national levels. Third, our inclusion criteria may limit the generalisability of the findings. For example, it was necessary to have an informant (someone that knows the older adult well) so that the schedule could be completed. In North Sumatra, 20.7% of participants listed were ineligible, all of which were because they did not have an informant available to participate. This could mean that those who are the most socially isolated are not adequately represented in our sample. However, the fact that 11.5% of both cohorts included informants that were not friends, family members or neighbours could indicate that this group might still be represented. Finally, there is the possibility of instrument-related diagnostic error as discussed above. However, within the present study we had very good convergent validity. It was able to differentiate a series of cognitive, functional and care outcomes, in addition to having good discrimination ability against other estimates of dementia.
Our study provides novel, empirical evidence on the high numbers of people aged 65 years and older with dementia in Indonesia and South Africa, and the low level of current diagnosis in these communities. The findings are an improvement on existing estimates in terms of the quality of sampling and diagnostic methodology used. In adopting a robust yet pragmatic approach to estimating dementia prevalence, we present the STRiDE methodology that can be used within other LMIC settings in the future. There are also questions raised by the relatively high prevalence rates observed in this study compared with other international estimates, but even with this uncertainty, it is clear that dementia is common and should be accorded policy priority within each country. The fact that so few participants received a formal diagnosis highlights the size of the problem. Future research needs to explore how people's lives are affected by dementia within LMICs and the costs of care, particularly with the knowledge that health and social care systems are not sufficient to fully support people with dementia anywhere in the world.
Supplementary material
Supplementary material is available online at https://doi.org/10.1192/bjo.2023.76
Data availability
Data will become available on UK Data Services in 2023 and is available from the corresponding author, N.F.
Acknowledgements
We thank researchers across countries for their hard work and diligence, in particular Ika Mariana Gultom, Eka Mahendrayana and Engki Irawan in Indonesia. We appreciate the sampling advice received from Dr Stephen Rule, from Outsourced Insights, and efforts of the fieldwork supervisors (Francois Lottering, Nwabisa Gunguluza and Mahlatse Moloto) in South Africa.
Author contributions
N.F. was responsible for data curation, formal analysis, methodology and project administration, wrote the original draft of the manuscript and reviewed and edited the manuscript. R.J. and I.T. were responsible for study investigation, methodology and supervision, and reviewed and edited the manuscript. Y.T. and M.S. were responsible for study conceptualisation, funding acquisition and methodology, and reviewed and edited the manuscript. F.I.F. supervised the study and reviewed and edited the manuscript. S.D., T.P.S. and A.I. were responsible for study methodology and reviewed and edited the manuscript. L.A. was responsible for study investigation and reviewed and edited the manuscript. E.A. was responsible for study conceptualisation and methodology, and reviewed and edited the manuscript. A.C.-H. and C.P.F. were responsible for funding acquisition and study methodology, and reviewed and edited the manuscript. P.D.T. was responsible for study methodology. I.G. was responsible for funding acquisition and reviewed and edited the manuscript. M.K. was responsible for study conceptualisation and funding acquisition, and reviewed and edited the manuscript. S.B. was responsible for study conceptualisation, funding acquisition, methodology and supervision, and reviewed and edited the manuscript.
Funding
This work was supported by the UK Research and Innovation's Global Challenges Research Fund (grant number ES/P010938/1). The funder has not influenced the design, outcome or interpretation of the study.
Declaration of interest
None.
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