Abstract
Alzheimer’s disease and Related Dementia (ADRD) is a growing concern for low- and middle-income countries. Yet, studies on the prevalence and risk factors for dementia in sub-Saharan Africa are limited. This study estimated the prevalence and identified the risk factors for ADRD in Ghana. A cross-sectional design involving 384 participants aged 60 years or more completed the Brief Community Screening Instrument for Dementia (CSID) with an additional set of questions on risk factors. The prevalence of dementia was 16% (62/384). Age (AOR = 1.031 (95% CI 1.002–1.061, p=0.035), education (AOR = 0.689 (95% CI 0.517–0.919, p=0.011), and employment (AOR = 0.320 (95% CI 0.149–0.685, p=0.004) were associated with dementia. Also, “experience of stressful life event from age 16–64” (AOR = 1.325 (95% CI 1.034–1.698, p=0.024), “experience of stressful life event from age 65+” (AOR = 1.258 (95% CI 1.024–1.546, p=0.042), and “activities of daily living” (AOR = 0.925 (95% CI 0.868–0.986, p=0.037) identified as risk factors of dementia. The burden of ADRD was high. Urgent actions are needed to address this problem. There is a possibility that the burden of dementia may have been overestimated because of the study instrument. Findings should be interpreted in light of this limitation.
Keywords: Lifestyle, sub-Saharan Africa, brief community screening instrument for dementia, stressful live events, activities of daily living, cognitive impairment
Introduction
Alzheimer’s disease and Related Dementia (ADRD) is a growing concern for low- and middle-income countries (LMICs). With the population aging, the number of people living with dementia is expected to grow rapidly in LMICs, particularly in sub-Saharan Africa (SSA). Projections indicate that by 2050, approximately 161 million persons who are 60 years or older will be residents of SSA (Guerchet et al., 2017a). This is likely to impose an increasing burden on health systems throughout SSA, as the country’s population ages, accompanied by rapid increases in the prevalence of vascular and other non-communicable disease risk factors for dementia (Olayinka & Mbuyi, 2014). The prevalence and incidence of dementia increase with age. Yet, there is only a handful of studies on the prevalence and risk factors for dementia in SSA that could inform context-specific interventions.
Ghana, a developing low and middle-income country in SSA, has seen rapid increases in the aging population over the past two decades, mainly due to the declining fertility rates and increasing life expectancy (Nyame et al., 2019). However, Alzheimer’s Disease and Related Dementia (ADRD) are largely understudied in Ghana. The latest World Health Organization (WHO) data published in 2018 indicated that deaths related to ADRD in Ghana reached 2,672 or 1.33% of total deaths (World Health Organization, 2018). The only study on prevalence conducted by the Kintampo Dementia Initiative (KDI), showed a standardized prevalence of 6.6% (95% CI-3.6–6.8), for all ages (Nyame et al., 2019). Regional estimates from population and hospital-based studies in SSA estimate the prevalence to range from 2.29–21.6% (Olayinka & Mbuyi, 2014). Similarly, another recent review with a meta-analysis of dementia in SSA (no studies from Ghana) noted a prevalence of 5.0% (Ojagbemi et al., 2021).
Estimating the population prevalence of ADRD in SSA, and identifying associated risk factors, has been identified as a public health priority (Guerchet et al., 2017a). Although age and sex seem to be consistently associated with dementia in SSA studies, the evidence around other risk factors such as smoking, alcohol use, physical inactivity, the experience of stressful life events, vascular events, and others has not been thoroughly investigated at the country level. For example, a longitudinal cohort study conducted by Gerritsen et al. (2017) in a Swedish sample reported that the experience of multiple negative life events at baseline predicted a higher risk for dementia. Similarly, unhealthy lifestyles such as excessive alcohol consumption, and inadequate participation in physical and social activities are associated with an increased risk of dementia (Sabia et al., 2018; Dhana et al., 2020; Nguyen et al., 2024). These risk factors are suggested to impact the life course similar to other chronic conditions of late life. However, the evidence is mostly based on studies carried out in high-income countries other than SSA. This study thus aimed to explore the association between these factors and dementia risk in the Ghanaian elderly population.
Accurate and timely assessment and diagnosis of dementia are essential in providing optimal clinical care and management to patients. However, the assessment and diagnosis of dementia in both primary care and at the population level are complex and can be difficult (Ferri & Jacob, 2017; Social Care Institute of Excellence, 2020). Part of the complexity and difficulty in diagnosing dementia stems from the fact that the symptoms of the condition could be mistaken as evidence of normal aging (Slavin et al., 2013; Ferri & Jacob, 2017). In low-resource settings, this difficulty is further compounded by limited access to healthcare, low health literacy, the stigma associated with the condition, and the limited capacity to screen and diagnose dementia (Maestre, 2012; Orikiriza, 2020).
There are many tests/tools available which can be administered to screen for the existence of dementia. Usually, screening entails cognitive testing for a history of cognitive and functional decline (Prince et al., 2011). Most of the existing tools for screening for dementia have limited utility in low-to-middle-income countries. For example, the Mini-Mental State Examination tool which is widely used in high-income countries is prone to educational and cultural bias (Ng et al., 2007). Additionally, the General Practitioner Assessment of Cognition (GPCOG), the Memory Impairment Screen (MIS), and the Mini-Cog have all been deemed not suited for settings with limited education such as Sub-Saharan Africa (Prince et al., 2011).
On the other hand, the Community Screening Instrument for Dementia (CSI-D) has been extensively used and validated across many settings including sub-Saharan Africa. Both the longer and shorter versions have proven to be reliable and valid (Prince et al., 2011). CSI-D has been used extensively in several sub-Saharan African countries including Nigeria (Yusuf et al., 2011), Tanzania (Paddick et al., 2014), South Africa (De Jager et al., 2017), and Uganda (Mubangizi et al., 2020). The strengths of this instrument are that it is not literacy dependent, and secondly, the inclusion of the informant interview provides insight into the cognitive and functional abilities of the subject thereby leading to a high probability of predicting the presence of dementia (Yusuf et al., 2011).
Given the lack of evidence, the need for more research in Ghana and SSA is obvious. The present study aimed to conduct a population-based study to estimate the prevalence and key modifiable and non-modifiable risk factors for ADRD in Ghana. Our findings will guide the health systems in Ghana and other countries in the SSA region with a similar healthcare system to accelerate the attention to these people and their families in the utilization of formal and informal health services for better health outcomes.
Materials and Methods
Study design
This was a quantitative community-based cross-sectional study. The study was carried out in six (6) randomly selected rural communities in the Juaben Municipal Assembly in the Ashanti Region and the Adentan Municipal Assembly in the Greater Accra Region. A multi-stage sampling method was employed by first randomly selecting two districts, followed by a random selection of three communities in each of the municipalities using a table of random numbers. Finally, in each community that was selected, a door-to-door survey was conducted in a random direction by trained research assistants in the Department of Health Promotion and Disability Studies of the Kwame Nkrumah University of Science and Technology. The first house to be visited was determined randomly by spinning a pen at the center of the community and the first house in the direction where the pen pointed became the starting point of the sample recruitment until the number of participants allocated to each community was reached.
The study was conducted among persons aged 60 years or older based on available evidence, which suggests that ADRD is more common among this subpopulation (WHO, 2017). In addition to the primary study participants, close relatives (refer to Table 2) of the primary respondents were also interviewed as part of the survey. The addition of the close relations of individuals suspected to have dementia enhances the validity of the data-gathering instrument used (Prince et al., 2011; Mubangizi et al., 2020). A minimum sample size of 384 was calculated based on an expected prevalence of 6.6.% and a precision of ± 5% at a 95% confidence level. The Committee on Human Research, Publications, and Ethics, an institutional review board of the Kwame Nkrumah University of Science and Technology, Ghana approved the study protocol. The ethical approval reference number is CHRPE/AP /057/21.
Table 2:
Socio-demographic Profile of Informants
| VARIABLE VALUE | MEAN (SD) | MINIMUM/MAXIMUM VALUE |
|---|---|---|
| Age (in completed years) | 38 (16.28) | 11 −82 |
| FREQUENCY (384) | PERCENTAGE (%) | |
| Highest Educational level | ||
| None | 32 | 8.33 |
| Primary school | 64 | 16.67 |
| Junior high/Middle school | 164 | 42.71 |
| Secondary school | 77 | 20.05 |
| Tertiary | 47 | 12.24 |
| Relationship to primary participant | ||
| Spouse | 41 | 10.68 |
| Sibling | 18 | 4.69 |
| Child | 148 | 38.54 |
| Grandchild | 66 | 17.19 |
| Other relatives | 58 | 15.10 |
| Non-biological relation | 53 | 13.80 |
Instrumentation
The study utilized the brief Community Screening Instrument for Dementia (CSID) which is a validated and reliable tool for estimating the prevalence of Alzheimer’s disease and related dementia(Prince et al., 2011; Mubangizi et al., 2020). The tool consists of two parts, a cognitive scale, and an informant scale. The former is for the primary respondent who is suspected to have dementia while the other part (informant scale) is for a close relation of the primary respondent. The addition of the informant scale is meant to validate the scores obtained from the cognitive scale for the index participant. The cognitive scale for the primary respondent was made up of seven items with a minimum score of 0 and a maximum score of 9. The rating score for the cognitive scale was as follows: 0–4 indicates probable dementia; 5–6 indicates possible dementia and 7–9 is deemed as normal. For the participants who scored 5–6, the researchers interviewed their close relations. In the end, the primary respondents were classified as screened positive for dementia if they had a CSID total score of ≤ 4. We included additional questions on correlates of dementia such as socio-demographic factors, family history, lifestyle, activities of daily living, and experience of stressful life events. Activities of daily living were assessed with eleven (11) items that were adopted and modified from a previous study (Gureje et al., 2006) with a minimum and maximum total score of 0 and 33 respectively. The Likert scale adopted ranged from 0 (unable to do) to 3 (can do without difficulty). A lower score indicated difficulty in performing activities of daily living. Experience of stressful life events was investigated for three different life periods: 0–15 years; 16–64 years; and 65 years and above. We adopted and modified the set of psychosocial risk factors previously described by Persson & Skoog (1996). For the experience of stressful life events from 0–15 years and 16–64 years, there were five (5) items each with a Yes/No response while for the experience of stressful life events from 65+, there were eight (8) items with a Yes/No response. A higher score indicated experience of more stressful life events. Data for this study were collected from May to June 2021.
Calculation of prevalence
Due to the potential of the brief CSID instrument to yield a higher prevalence of dementia over the true prevalence of dementia, we utilized the back estimation method previously described in a related subject (De Jager et al., 2017; Mubangizi et al., 2020) to estimate the true prevalence of dementia. We relied on the screened positive data from our study and the previously published sensitivity (0.95) and specificity (0.90) values of the brief CSID tool. These sensitivity and specificity values have been reported by Prince et al. (2011) and Mubangizi et al. (2020). Based on the sensitivity and specificity values of the brief CSID tool, we calculated the number of true positives, test positives, and test negatives. Test positives are participants who screened positive using the study instrument while test negative were participants without the outcome. These data were inputted into the following formula together with the established sensitivity and positivity values to estimate the true positives. Finally, the number of true positives was then used to estimate the true prevalence rate of dementia. The number of true positives was derived using:
Data analysis
All data analyses were performed using STATA software version 17. The dependent variable for the analysis was the presence/absence of dementia while the independent variables were the participants’ socio-demographic characteristics, lifestyle factors, and experience of stressful life events across the life course. All statistical tests were considered significant if the probability value was less than 0.05 (P-value <0.05).
Results
Socio-demographics of primary participants
The mean age of primary participants was 72 years (SD=10.22). The majority of participants were females (69%), and Christianity was the dominant religion that participants disclosed affiliation with (87%). The majority of participants had “Junior high school” as their highest educational attainment (40%), with 33% having no formal education. As regards marital status, the majority of participants (45%) were widows/widowers; 40% were married. The majority of participants (58%) were unemployed. There was a participant response rate of 100%. Further details of participants’ characteristics are presented in Table 1. The mean age of the informant participants was 38 years (SD= 16.28). The majority of the informants were also females (69%). More than a third (42.71%) of the informants had “Junior high school” as their highest level of educational attainment. Most of the informants were biologically related to the primary participants.
Table 1:
Socio-demographic profile of participants
| VARIABLE | MEAN (SD) | MINIMUM VALUE/ MAXIMUM VALUE |
|---|---|---|
| Age (in completed years) | 72 (10.22) | 60 – 130 |
| FREQUENCY (n=384) | PERCENTAGE (%) | |
| Marital Status | ||
| ○ Married | 153 | 40 |
| ○ Single | 3 | 0.8 |
| ○ Cohabiting | 1 | 0.2 |
| ○ Divorced | 55 | 14 |
| ○ Widowed | 171 | 45 |
| Highest Educational Level | ||
| ○ No formal education | 127 | 33 |
| ○ Primary school | 58 | 15 |
| ○ Junior high school | 152 | 40 |
| ○ Senior high school | 14 | 4 |
| ○ Tertiary | 33 | 9 |
| Employment Status | ||
| ○ Unemployed | 222 | 58 |
| ○ Employed | 162 | 42 |
| Religious Affiliation | ||
| ○ Christianity | 335 | 87 |
| ○ Islam | 33 | 9 |
| ○ African Traditional Religion | 8 | 2 |
| ○ Other | 8 | 2 |
Prevalence of dementia
In the study sample of 384 participants who were screened, 13 (3.39%) of them recorded a CSID cognitive score of ≤ 4. Out of the 384 respondents, another 74 (19.27%) had a CSID cognitive score of 5 or 6. For these 74 participants, the informant score was subtracted from the corresponding primary participants’ CSID cognitive score. The resultant data showed that 44/74 had a CSID total score of ≤ 4. Therefore, the total number of participants who screened positive for probable dementia based on the combined CSID cognitive score and the CSID total score was 57 (15%) obtained by the addition of 13 and 44. We then used the back estimation method already described to estimate the true prevalence. From the estimation, the true positives were 62 thereby giving a prevalence rate of 16% (62/384) with a positive predictive value (PPV) of 62% and a negative predictive value (NPV) of 99% (Table 3). Participants who fall within the category of ‘possible dementia’ were 8% (30/384), while the remaining participants (77%/297) were identified as ‘normal’. As regards the regional distribution of probable dementia, it was observed that the condition was more prevalent in the Ashanti region (17%) than in the Greater Accra region (12%). Table 4 has some additional information on the regional distribution of the condition.
Table 3:
Estimates of prevalence based on sensitivity & specificity calculations
| CATEGORIES | FREQUENCY | PERCENTAGE |
|---|---|---|
| Apparent prevalence | 57 | 15 |
| True prevalence | 62 | 16 |
| Sensitivity | - | 95 |
| Specificity | - | 90 |
| Positive predictive value | - | 62 |
| Negative predictive valued | - | 99 |
Table 4:
Lifestyle and psychosocial risk factors
| VARIABLE | MEAN (SD) | MINIMUM VALUE/ MAXIMUM VALUE |
|---|---|---|
| ADL | 29.59 (4.35) | 0–33 |
| Experience of stressful life events (0–15) | 1.46 (1.18) | 0–4 |
| Experience of stressful life events (16–64) | 2.25 (1.27) | 0–5 |
| Experience of stressful life events (65+) | 2.13 (1.76) | 0–8 |
| Average no. of days in a week spent doing moderate exercise | 3.31 (2.22) | 0–7 |
| Average minutes spent doing moderate exercise in a day | 89.04 (83.98) | 10–510 |
| Average number of days in a week spent walking | 3.92 (2.29) | 1–7 |
| Average minutes spent walking in a day | 75.83 (80.04) | 10–600 |
| FREQUENCY (n=384) | PERCENTAGE (%) | |
| Smoking status | ||
| ○ Never Smoked | 320 | 83.33 |
| ○ Ever smoked | 55 | 14.32 |
| ○ Currently smoking | 9 | 2.34 |
| Alcohol consumption | ||
| ○ Yes | 103 | 26.82 |
| ○ No | 281 | 73.18 |
| History of stroke | ||
| ○ Yes | 43 | 11.20 |
| ○ No | 341 | 88.80 |
| Experience of head injury | ||
| ○ Yes | 93 | 24.22 |
| ○ No | 291 | 75.78 |
Lifestyle and psychosocial risk factors
The findings indicated that most of the participants were able to perform the activities of daily living such as bathing, dressing, reaching, and toileting (29.59±4.35). The experience of stressful life events from age 0–15 was minimal (1.46±1.18) compared with the experience of stressful life events from age 16–64 and 65+. Further, most of the participants (83.33%) had never smoked while nearly a fourth had a history of head injury (24.22%). The lifestyle risk factors are presented in Table 4.
Factors Associated with Dementia
Socio-demographics and probable dementia
Socio-demographic variables showing significant association with probable dementia in a binary logistic regression model were index participants’ age, education, religion, and employment; sex and marital status did not show significant association. When these variables (i.e., showing significant association) were further examined in a multivariable logistic regression model, age (p=0.035; AOR=1.031; 95% CI 1.002 – 1.061), education (p=0.011; AOR=0.689; 95% CI 0.517 – 0.919) and employment (p=0.004; AOR=0.320; 95% CI 0.149–0.685) retained a significant association with probable dementia. Whereas age had a positive association with probable dementia, education, and employment both had a negative association with probable dementia. Additional information is presented in Table 5.
Table 5:
Socio-Demographics and Probable Dementia
| Variables | Probable Dementia | |||
|---|---|---|---|---|
| Screened Prevalence % | Crude p-value | Adjusted p-value [Beta Coef.]** | Adjusted Odds Ratio [95% CI]** | |
| Age | 0.000 | 0.035 [0.030]* | 1.031 [1.002–1.061] | |
| Education | ||||
| ○ None | 25.2 | 0.000 | 0.011 [−0.371] * | 0.689 [0.517–0.919] |
| ○ Primary school | 13.8 | |||
| ○ Junior High School | 9.9 | |||
| ○ Senior High School | 0.0 | |||
| ○ Tertiary | 2.0 | |||
| Religion | ||||
| ○ Christianity | 13.1 | 0.007 | 0.060 [−0.412] | 0.662 [0.431–1.016] |
| ○ Islam | 21.2 | |||
| ○ African Traditional | 37.5 | |||
| ○ Non-religious | 37.5 | |||
| Employment | ||||
| ○ Unemployed | 21.2 | 0.000 | 0.004 [−1.145] * | 0.320 [0.149–0.685] |
| ○ Employed | 6.2 | |||
| Sex | ||||
| ○ Male | 12.5 | 0.385 | - | - |
| ○ Female | 15.9 | |||
| Marital Status | ||||
| ○ Cohabiting | 0.0 | 0.409 | - | - |
| ○ Single | 33.3 | |||
| ○ Divorced | 12.7 | |||
| ○ Widowed | 18.1 | |||
| ○ Married | 11.8 | |||
Explanatory variables included in a multivariable logistic regression model were age, education, religion, and employment
Lifestyle factors and probable dementia
Lifestyle factors that showed significant association with probable dementia in a binary logistic regression analysis were; “experience of stressful life events from age 16–64”, “experience of stressful life events from age 65+”, and “activities of daily living”. Each of the aforementioned variables was examined further in a multivariable logistic regression model adjusting for socio-demographic variables – age, education, religion, and employment. All three lifestyle variables retained statistically significant association, though ‘experience of stressful life event from age 65+’ had a relatively weak association. Both ‘experience of stressful life event from age 16–64’ and ‘experience of stressful life event from age 65+’ showed a positive association with probable dementia (p=0.024; AOR=1.325; 95% CI 1.034–1.698 and p=0.042; AOR=1.258; 95% CI 1.024–1.546 respectively), while ‘activities of daily living had a negative association with probable dementia (p=0.037; AOR=0.925; CI 0.868–0.986).
On the other hand, variables including smoking status, alcohol behavior, physical activity, history of stroke, and an experience of head injuries did not show any statistically significant association with probable dementia in a binary logistic regression analysis. Additional information is presented in Table 6.
Table 6:
Lifestyle Factors and probable dementia
| Variables | Probable Dementia | ||
|---|---|---|---|
| Crude p-value | Adjusted p-value [Beta Coef.]** | Adjusted Odds Ratio [95% CI]** | |
| Experience of stressful life events from age 16–64 | 0.003 | 0.024 [0.282] | 1.325 [1.034–1.698] |
| Experience of stressful life events from age 65+ | 0.000 | 0.042 [0.212] | 1.258 [1.024–1.546] |
| Activities of daily living | 0.000 | 0.037 [−0.065] | 0.925 [0.868–0.986] |
| Smoking status | 0.314 | - | - |
| Alcohol behavior | 0.427 | - | - |
| Physical activity (vigorous exercise, moderate exercise) | 0.619 0.185 |
- | - |
| History of Stroke | 0.791 | - | - |
| Experience of head injuries | 0.788 | - | - |
Explanatory variables were adjusted for age, education, religion, and employment
Discussion
Prevalence of dementia
In this study of 384 older adults from Ghana, we estimated the population prevalence of probable dementia to be 16% based on the sensitivity and specificity analysis described above while the apparent prevalence was 15%. In Europe, the prevalence of dementia has been estimated at 5.05%, lower than that found in our study (Niu et al., 2017). Similarly, about 5.0% of Americans aged 65 −74 are living with dementia, a rate that is lower than what we found in the current study (Alzheimer’s Association, 2024). The disparities in the prevalence rate between the current study and those reported in Europe and America could be attributable to diagnostic tools deployed coupled with variations in the age ranges of the study population.
Furthermore, in Uganda (Mubangizi et al., 2020) and South Africa (De Jager et al., 2017) where a similar screening tool was used, the prevalence of dementia based on the back estimation method in our study is higher than the apparent prevalence. This discrepancy could be a result of the variations in the actual prevalence of dementia in the screened population in the different countries and or the sensitivity and specificity values used in the estimation. The estimated probable prevalence in this study is higher than the 6.38% noted in the report by Alzheimer’s Disease International in 2017 (Guerchet et al., 2017b) and the 5.0% reported in the recent meta-analysis of studies in SSA (Ojagbemi et al., 2021). Recently, studies in Uganda (Mubangizi et al., 2020) and Tanzania (Longdon et al., 2013) using a similar screening tool and with a similar age distribution, recorded a prevalence of 20% and 15.4% respectively. The higher prevalence of dementia in the current study and previous studies in Uganda (Mubangizi et al., 2020) and Tanzania (Longdon et al., 2013) could be a result of the methodology used – door-to-door screening rather than hospital-based screening and detection. This is because when the Diagnostic and Statistical Manual of Mental Disorders (4th edition) tool was applied to the same sample in the Tanzanian study, the prevalence of probable dementia dropped to 6.4%. It has been noted that the CSID screening tool yields high prevalence estimates compared with structured clinical interviews explaining the high prevalence in our study and those in Uganda and Tanzania. However, with an NPV value of nearly 100%, the probability that a participant with normal cognitive functioning was screened as positive in the current study was very minimal. Secondly, the choice of the brief CSID was influenced by its suitability for use by non-specialists in a low-resource setting like Ghana (Prince et al., 2010; Mubangizi et al., 2020).
Socio-demographic factors and dementia
Consistent with other findings in the literature, our study suggested that age is an important factor associated with dementia both at the bivariate and multivariate levels. The odds of having dementia increased with advancing age in this study population. This finding is supported by a similar study conducted in Rwanda which found that probable dementia positively correlated with age even after adjusting for possible confounders (Mubangizi et al., 2020). One of the plausible explanations is that aging is accompanied by changes in brain health including activation of inflammation and weakening of the neurons in areas related to memory (Longdon et al., 2013). Also, our findings showed that formal education had an inverse association with probable dementia. Again, the association between fewer years of schooling and the experience of dementia is well established. In one study, the investigators found that the risk of dementia was twice as high among participants with fewer years of schooling compared to those with more years of schooling (Wu et al., 2011). From the literature, it has been established that formal education or staying longer in school is protective against the development of dementia (Sharp & Gatz, 2011; Langa et al., 2017). One of the plausible explanations for this association is that education helps the brain to develop more synapses that may boost a person’s cognitive reserve thereby helping to prevent dementia. Besides, highly educated people tend to have a healthier lifestyle than those with less education. For instance, people with more education may be aware of the dangers associated with smoking, lack of exercise, and poor nutrition and thus may be motivated to adopt healthier choices.
Additionally, the current study observed that the risk of dementia was associated with being unemployed compared to being employed. Several studies have established a correlation between being unemployed or retired and the risk of dementia (Mythily et al., 2015; Kivimäki et al., 2021). The protection offered by being employed could be attributed to the cognitive stimulation offered by the execution of job-related activities particularly mentally stimulating occupations. Furthermore, the financial returns from being employed and the meaning, purpose, and satisfaction derived from the same may also insulate people from stress or societal pressures that can be damaging to an individual’s mental health and well-being.
The current study did not find any statistically significant association between religious affiliation and dementia. This finding is at variance with a study conducted by Lin and his colleagues in a Taiwanese sample where a strong correlation was established (Lin et al., 2015). The investigators found that participants with affiliation to Christianity showed a decreased dementia risk (adjusted odds ratio [AOR] = 0.46, 95% confidence interval [CI] = 0.25–0.87) compared with those without any religious affiliation. One of the possible explanations for this association is that involvement in religious activities promotes active and stimulating social engagement which are vital in slowing cognitive decline. The lack of statistical significance in our study could thus be attributed to possible variations in their level of active engagement in the activities of their particular religion(Holtzman et al., 2004; Moxey et al., 2011).
Lifestyle factors and dementia
From the results, the primary participants who experienced notable stress from age 16 to 64 years were 1.3 times more likely to have probable dementia. Similarly, index participants who indicated having experienced notable stress from age 65 years were 1.2 times more likely to have probable dementia. Stress and its association with dementia have been reported by several authors (Radford et al., 2017; Nabe-Nielsen et al., 2020; Sindhi et al., 2017). A recent systematic review and meta-analysis by Severs et al. found that the experience of traumatic events such as war trauma and childhood trauma was associated with an increased risk of dementia. Conversely, in a longitudinal study involving the adult population of Sweden, the investigators did not find an association between participants’ experience of stressful life events and dementia (Sundström et al., 2014). As Sundstrom et al. (2014) have previously noted, the contradictory findings in the literature regarding the association between stressful life events and dementia risk to a certain degree might be due to differences in the study methodologies used. Another possible reason for this difference is the variation in individual responses to stressful life events. One individual might consider a certain event as extremely stressful whereas another might perceive it as rather trivial thereby subsequently producing differential outcomes in a person’s life.
As regards index participants’ “activities of daily living” (ADL) and its association with probable dementia, it can be observed from the results that a participant was less likely to have probable dementia, for any given unit increase in the ADL of that participant. Thus, ADL was useful in reducing the likelihood of a participant having probable dementia. In a recent study conducted in Uganda in which authors explored the potential association between an ADL-related variable “physical activity” and probable dementia, authors reported an inverse significant association between the two variables which corroborates the findings of our study (Mubangizi et al., 2020).
Similar to the findings of the study conducted in Uganda our study did not establish a significant association between the variables smoking, alcohol use, and vascular accidents on one hand, and probable dementia on the other hand (Mubangizi et al., 2020). There are a couple of reasons that could explain why these variables did not present as risk factors in this study despite their known association with dementia. First, it is possible that the sample size of 384 was not sufficiently large to detect the existence of a possible association between these known risk factors and dementia. Second, the lack of association between these factors and dementia could be attributed to the intensity of these factors in the study population. For example, a previous study established a higher risk of dementia in people who abstain from alcohol or consume >14 units/week compared with long-term moderate consumption of 1–14 units/week (Sabia et al., 2018). Concerning the link between smoking and the risk of dementia, previous studies have suggested that an epigenetic mechanism may be involved (Kawakami et al., 2023). For example, Kawakami et al. (2023) observed that the dementia risk associated with smoking was higher in middle-aged people (<65 years) compared with older people (≥65 years). These findings confirm the complex relationships between these risk factors and the risk of developing dementia.
Limitations of the study
The current study is subject to a few limitations that need to be acknowledged. First, the screening tool (CSID) employed in this study has the potential to overestimate the actual prevalence of dementia due to its ability to pick out early dementia or mild cognitive impairment. Despite this, the brief CSID has proven to be a valid and reliable screening tool for dementia (De Jager et al., 2017; Mubangizi et al., 2020). Second, the present study relied on self-reported data which is subject to the possibility of recall bias especially when participants are asked to recollect historical information. Finally, other important risk factors for dementia such as obesity, diabetes, hearing loss, and hypertension were not examined in this study considering the challenges one could potentially encounter in investigating all possible risk factors in a single study.
Despite these limitations, the present study provides valuable population-based information for planning and designing supportive interventions, policy directions, and research agendas for Alzheimer’s disease and related dementia in Ghana and elsewhere in SSA.
Conclusion
We found a higher prevalence of dementia in six rural communities in Ghana than what has been previously reported. Although the prevalence rate is somewhat comparable to similar studies elsewhere in SSA, the relatively high rate should be a major source of concern for the public health community considering that the disease burden is projected to increase in the foreseeable future. Older age, lower education, being unemployed, decreased functioning in activities of daily living, and experience of stressful life events were found to be associated with dementia risk. Although there is currently limited evidence to support a cause-effect relationship between any preventative strategy and the development of dementia, we recommend that improving access to educational and employment opportunities will help address some of the identified risk factors. In addition, we recommend that staying physically active and maintaining connections with family and friends is likely to contribute to alleviating decreased functioning in activities of daily and the experience of stressful life events respectively.
In terms of directions for future research, we suggest that similar studies should be carried out in other parts of the country to ascertain the overall burden of dementia in Ghana. Secondly, we recommend that future studies in Ghana and elsewhere in SSA should explore other known risk factors of dementia such as diabetes, hypertension, hyperlipidemia, depression, epilepsy, and genetic polymorphisms which were not examined in this study to ascertain their relevance in the sub-Saharan population.
Acknowledgments
This study was funded by grant D43-TW007267 from the Fogarty International Center, US National Institutes of Health. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. We wish to thank the study respondents for their willing participation in this study. Finally, our sincere gratitude goes to all the research assistants at the Department of Health Promotion and Disability Studies at the Kwame Nkrumah University of Science and Technology, Kumasi who assisted with the data collection.
Footnotes
Competing interests: The authors declare that they have no competing interests
Ethics approval and consent to participate
Ethical clearance was obtained from the Committee on Human Research, Publication, and Ethics, an institutional review board at Kwame Nkrumah University of Science and Technology, Ghana. Informed consent was obtained from all participants and the study was implemented per relevant guidelines/regulations, including the Declaration of Helsinki.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author, [PO], upon reasonable request.
References
- Alzheimer’s Association (2024) Alzheimer’s Association 2024 Alzheimer’s Disease Facts and Figures. Chicago, USA. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dhana K, Evans DA, Rajan KB, Bennett DA & Morris MC (2020) Healthy lifestyle and the risk of Alzheimer dementia: Findings from 2 longitudinal studies. Neurology, 95 (4), pp.E374–E383. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ferri CP & Jacob KS (2017) Dementia in low-income and middle-income countries: Different realities mandate tailored solutions. PLoS Medicine, 14 (3), pp.2–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gerritsen L, Wang HX, Reynolds CA, Fratiglioni L, Gatz M & Pedersen NL (2017) Influence of Negative Life Events and Widowhood on Risk for Dementia. American Journal of Geriatric Psychiatry, 25 (7), pp.766–778. Available from: < 10.1016/j.jagp.2017.02.009>. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guerchet M, Mayston R, Lloyd-Sherlock P, Prince M, Aboderin I, Akinyemi R, Paddick S-M, Wimo A, Amoakoh-Coleman M, Uwakwe R and & Ezeah P (2017a) Dementia in Sub-Saharan Africa: Challenges and opportunities.
- Guerchet M, Mayston R, Lloyd-Sherlock P, Prince M, Aboderin I, Akinyemi R, Paddick S-M, Wimo A, Amoakoh-Coleman M, Uwakwe R and & Ezeah P (2017b) Dementia in Sub-Saharan Africa: Challenges and opportunities. London, UK, Alzheimer’s Disease International. Available from: <https://www.alzint.org/u/dementia-sub-saharan-africa.pdf>. [Google Scholar]
- Gureje O, Ogunniyi A & Kola L (2006) The profile and impact of probable dementia in a sub-Saharan African community: results from the Ibadan Study of Aging. Journal of Psychosomatic Research, 61 (3), pp.327–333. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holtzman RE, Rebok GW, Saczynski JS, Kouzis AC, Doyle KW & Eaton WW (2004) Social Network Characteristics and Cognition in Middle-Aged and Older Adults., 59 (6), pp.278–284. [DOI] [PubMed] [Google Scholar]
- De Jager CA, Msemburi W, Pepper K & Combrinck MI (2017) Dementia Prevalence in a Rural Region of South Africa: A Cross-Sectional Community Study. Journal of Alzheimer’s Disease, 60 (3), pp.1087–1096. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kawakami S, Yamato R, Kitamura K, Watanabe Y, Kabasawa K, Takahashi A, Saito T, Kobayashi R, Oshiki R, Takachi R, Tsugane S, Yamazaki O, Watanabe K & Nakamura K (2023) Alcohol consumption, smoking, and risk of dementia in community-dwelling Japanese people aged 40–74 years: The Murakami cohort study. Maturitas, 176 (June). [DOI] [PubMed] [Google Scholar]
- Kivimäki M, Walker KA, Pentti J, Nyberg ST, Mars N, Vahtera J, Suominen SB, Lallukka T, Rahkonen O, Pietiläinen O, Koskinen A, Väänänen A, Kalsi JK, Goldberg M, Zins M, Alfredsson L, Westerholm PJM, Knutsson A, Theorell T, Ervasti J, Oksanen T, Sipilä PN, Tabak AG, Ferrie JE, Williams SA, Livingston G, Gottesman RF, Singh-Manoux A, Zetterberg H & Lindbohm JV (2021) Cognitive stimulation in the workplace, plasma proteins, and risk of dementia: Three analyses of population cohort studies. The BMJ, 374. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Langa KM, Larson EB, Crimmins EM, Faul JD, Levine DA, Kabeto MU & Weir DR (2017) A comparison of the prevalence of dementia in the United States in 2000 and 2012. JAMA Internal Medicine, 177 (1), pp.51–58. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lin KP, Chou YC, Chen JH, Chen CD, Yang SY, Chen TF, Sun Y, Wen LL, Yip PK, Chu YM & Chen YC (2015) Religious affiliation and the risk of dementia in Taiwanese elderly. Archives of Gerontology and Geriatrics, 60 (3), pp.501–506. Available from: < 10.1016/j.archger.2015.01.009>. [DOI] [PubMed] [Google Scholar]
- Longdon AR, Paddick SM, Kisoli A, Dotchin C, Gray WK, Dewhurst F, Chaote P, Teodorczuk A, Dewhurst M, Jusabani AM & Walker R (2013) The prevalence of dementia in rural Tanzania: A cross-sectional community-based study. International Journal of Geriatric Psychiatry, 28 (7), pp.728–737. [DOI] [PubMed] [Google Scholar]
- Maestre GE (2012) Assessing dementia in resource-poor regions. Current Neurology and Neuroscience Reports, 12 (5), pp.511–519. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moxey A, Mcevoy M, Bowe S & Attia J (2011) Spirituality, religion, social support and health among older Australian adults., 30 (2), pp.82–88. [DOI] [PubMed] [Google Scholar]
- Mubangizi V, Maling S, Obua C & Tsai AC (2020) Prevalence and correlates of Alzheimer ‘ s disease and related dementias in rural study. BMC Geriatrics, 20 (48), pp.1–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mythily S, Chong SA, Vaingankar JA, Abdin E & Chua BY (2015) Prevalence of dementia in people aged 60 years and above: Results from the WiSE study. Journal of Alzheimer’s Disease, 45 (4), pp.1127–1138. Available from: < 10.3233/JAD-142769>. [DOI] [PubMed] [Google Scholar]
- Nabe-Nielsen K, Rod NH, Hansen ÅM, Prescott E, Grynderup MB, Islamoska S, Ishtiak-Ahmed K, Garde AH, Gyntelberg F, Mortensen EL, Phung TKT, Waldemar G & Westendorp RGJ (2020) Perceived stress and dementia: Results from the Copenhagen city heart study. Aging and Mental Health, 24 (11), pp.1828–1836. [DOI] [PubMed] [Google Scholar]
- Ng TP, Niti M, Chiam PC & Kua EH (2007) Ethnic and educational differences in cognitive test performance on mini-mental state examination in Asians. American Journal of Geriatric Psychiatry, 15 (2), pp.130–139. Available from: < 10.1097/01.JGP.0000235710.17450.9a>. [DOI] [PubMed] [Google Scholar]
- Nguyen HXT, Bradley K, McNamara BJ, Watson R, Malay R & LoGiudice D (2024) Risk, protective, and biomarkers of dementia in Indigenous peoples: A systematic review. Alzheimer’s and Dementia, 20 (1), pp.563–592. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Niu H, Álvarez-Álvarez I, Guillén-Grima F & Aguinaga-Ontoso I (2017) Prevalencia e incidencia de la enfermedad de Alzheimer en Europa: metaanálisis. Neurologia, 32 (8), pp.523–532. Available from: < 10.1016/j.nrl.2016.02.016>. [DOI] [PubMed] [Google Scholar]
- Nyame S, Agyeman N, Danso S, Ae-Ngibise KA & Asante KP (2019) Dementia research needs in Ghana: a perspective. Journal of Global Health Reports, 3. [Google Scholar]
- Ojagbemi A, Okekunle AP & Babatunde O (2021) Dominant and Modifiable Risk Factors for Dementia in Sub-Saharan Africa: A Systematic Review and Meta-Analysis. Frontiers in Neurology, 12 (March), pp.1–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Olayinka OO & Mbuyi NN (2014) Epidemiology of Dementia among the Elderly in Sub-Saharan Africa. International Journal of Alzheimer’s Disease, 2014. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Orikiriza P (2020) Dementia 2019: Challenges of diagnosing dementia among elderly patients in a rural Referral Hospital, South-Western Uganda. Journal of Health and Medical Research, 2 (2). [Google Scholar]
- Paddick SM, Longdon A, Kisoli A, Gray WK, Dotchin CL, Jusabani A, Iqbal A, Hughes J, Teodorczuk A, Chaote P & Walker RW (2014) The prevalence of dementia subtypes in rural Tanzania. American Journal of Geriatric Psychiatry, 22 (12), pp.1613–1622. Available from: < 10.1016/j.jagp.2014.02.004>. [DOI] [PubMed] [Google Scholar]
- Persson G & Skoog I (1996) A prospective population study of psychosocial risk factors for late onset dementia. International Journal of Geriatric Psychiatry, 11, pp.15–22. [Google Scholar]
- Prince M, Acosta D, Ferri CP, Guerra M, Huang Y, Jacob KS, Llibre Rodriguez JJ, Salas A, Sosa AL, Williams JD & Hall KS (2011) A brief dementia screener suitable for use by non-specialists in resource poor settings-the cross-cultural derivation and validation of the brief Community Screening Instrument for Dementia. International Journal of Geriatric Psychiatry, 26 (9), pp.899–907. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Radford K, Delbaere K, Draper B, Mack HA, Daylight G, Cumming R, Chalkley S, Minogue C & Broe GA (2017) Childhood Stress and Adversity is Associated with Late-Life Dementia in Aboriginal Australians. American Journal of Geriatric Psychiatry, 25 (10), pp.1097–1106. [DOI] [PubMed] [Google Scholar]
- Sabia S, Fayosse A, Dumurgier J, Dugravot A, Akbaraly T, Britton A, Kivimäki M & Singh-Manoux A (2018) Alcohol consumption and risk of dementia: 23 year follow-up of Whitehall II cohort study. BMJ (Online), 362. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sharp ES & Gatz M (2011) Relationship between education and dementia: An updated systematic review. Alzheimer Disease and Associated Disorders, 25 (4), pp.289–304. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sindhi S, Hagman G, Hakansson K, Kulmala J & Nilson C (2017) Midlife Work-Related Stress Increases Dementia Risk in Later Life: The CAIDE 30-Year Study. Journals of Gerontology - Series B Psychological Sciences and Social Sciences, 72 (6), pp.1044–1053. Available from: < 10.1093/geronb/gbw043>. [DOI] [PubMed] [Google Scholar]
- Slavin MJ, Brodaty H & Sachdev PS (2013) Challenges of diagnosing dementia in the oldest old population. Journals of Gerontology - Series A Biological Sciences and Medical Sciences, 68 (9), pp.1103–1111. [DOI] [PubMed] [Google Scholar]
- Social Care Institute of Excellence (2020) Getting a dementia diagnosis [Internet]. Available from: <https://www.scie.org.uk/dementia/symptoms/diagnosis/getting-a-diagnosis.asp> [Accessed 10 January 2023].
- Sundström A, Rönnlund M, Adolfsson R & Nilsson LG (2014) Stressful life events are not associated with the development of dementia. International Psychogeriatrics, 26 (1), pp.147–154. [DOI] [PMC free article] [PubMed] [Google Scholar]
- World Health Organization (2018) Key messages: Prevalence of dementia worldwide. Geneva, World Health Organization. [Google Scholar]
- Wu MS, Lan TH, Chen CM, Chiu HC & Lan TY (2011) Socio-demographic and health-related factors associated with cognitive impairment in the elderly in Taiwan. BMC Public Health, 11 (1), p.22. Available from: <http://www.biomedcentral.com/1471-2458/11/22>. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yusuf AJ, Baiyewu O, Sheikh TL & Shehu AU (2011) Prevalence of dementia and dementia subtypes among community-dwelling elderly people in northern Nigeria. International Psychogeriatrics, 23 (3), pp.379–386. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The data that support the findings of this study are available from the corresponding author, [PO], upon reasonable request.
