The Impact of Disease Registries on Advancing Knowledge and Understanding of Dementia Globally

Abstract

To help address the increasing challenges related to the provision of dementia care, dementia registries have emerged around the world as important tools to gain insights and a better understanding of the disease process. Dementia registries provide a valuable source of standardized data collected from a large number of patients. This review explores the published research relating to different dementia registries around the world and discusses how these registries have improved our knowledge and understanding of the incidence, prevalence, risk factors, mortality, diagnosis, and management of dementia. A number of the best-known dementia registries with high research output including SveDem, NACC, ReDeGi, CREDOS and PRODEM were selected to study the publication output based on their data, investigate the key findings of these registry-based studies. Registries data contributed to understanding many aspects of the disease including disease prevalence in specific areas, patient characteristics and how they differ in populations, mortality risks, as well as the disease risk factors. Registries data impacted the quality of patients’ lives through determining the best treatment strategy for a patient based on previous patient outcomes. In conclusion, registries have significantly advanced scientific knowledge and understanding of dementia and impacted policy, clinical practice care delivery.

Introduction

Dementia, Alzheimer’s disease (AD) and other neurodegenerative diseases are considered to be a major societal challenge (Weiner et al., 2018). The advancements in education, housing and sanitation, as well as, improvements in healthcare services, have all contributed to increasing people’s life span and decreasing mortality. However, living longer has resulted in an increase in the prevalence of age-related conditions, including dementia. Dementia is a devastating disorder that is defined as “A syndrome, usually of chronic or progressive nature, caused by a variety of brain illnesses that affect memory, thinking, behavior and ability to perform everyday activities” (WHO, 2012). The number of people with dementia is estimated to triple in 2050, and hence, the disease is considered a public health priority by the WHO (2018). In addition to the impairment in memory and cognition, dementia affects day to day function and leads to an increased dependency (Liu-Seifert et al., 2015). The estimated annual cost of dementia care per person is estimated to be $32865 in high income countries, $6827 in upper-middle income countries and $3109 in lower middle-income countries (WHO, 2017). A comprehensive approach to patient care that results in an improvement in patients’ lives will be an effective way to decrease the costs and address this global health burden. The availability of accurate disease data is crucial to determine the risk factors of the disease and identify targets for treatment and prevention.

Disease registries are considered one of the most cost-effective ways of collecting patient information and longitudinal follow-up data that can be used for research purposes as well as clinical observations (Gliklich et al., 2012). The availability of datasets together with the advances in data analytic techniques has allowed the reporting of insightful new data and perspectives in the field of dementia. This paper aims to review studies that were based on registry data and evaluate the impact of these studies on advancing the diagnostic and treatment procedures for better disease monitoring, as well as, increasing our knowledge in the field. Specifically, this review (1) describes the publication output of a number of the best-known dementia registries with high publication output, particularly SveDem, NACC, ReDeGi, CREDOS and PRODEM, (2) investigates the objectives and key findings of the registry-based studies to discuss how we have benefited from the data in terms of knowledge of the incidence of dementia in different populations, as well as the factors that increase patients’ mortality risk, and (3) studies the impact of registry findings on disease management and improved diagnostic procedures, treatment practices and advance our general knowledge of the disease will also be discussed.

Background: Dementia Registries Around the World and Their Importance

The imperative to tackle the impact of chronic diseases has led to the establishment of disease registries to collect patient data and gain insights into the cause and pathogenesis of these illnesses (Richesson and Vehik, 2010). Registries differ in definitions and classifications according to their purpose, reporting method and the type of data included (Richesson and Vehik, 2010); however, a registry is generally a system of ongoing documentation of patients’ data with a particular disease (Krysinska et al., 2017). Different types of patient registries are increasingly being developed to address the needs of healthcare systems all over the world (Hopper, 2017).

The first disease registries were developed in Scandinavian countries such as Denmark, Finland and Sweden and have continued to grow to include many different diseases and data from medical records including demographic and personal characteristics (Frank, 2000). In contrast, to our knowledge, the United States was the first country to establish a registry for dementia disorders when they created the Consortium to Establish a Registry for Alzheimer’s Disease (CERAD) that aimed to evaluate the accuracy of AD diagnosis (Krysinska et al., 2017). Subsequently, other dementia registries were developed all over the world consisting of large databases of dementia patients to enable studies on causes, risk factors, prevalence and other variables related to the disease, e.g., London, Newcastle, and the Creutzfeldt-Jakob register in Edinburgh (Leach and Levy, 1993). The National Alzheimer’s Coordinating Center (NACC) is one of the older registries that was established in the United States in 1990 to collect standardized clinical data on patients with Alzheimer’s disease (Beekly et al., 2004). The NACC includes standardized and longitudinal data in addition to the autopsy data for patients with AD that have been used in studies to investigate symptoms, diagnosis, genetics, biomarkers, as well as clinical practices and mortality risk in dementia (Krysinska et al., 2017).

More recently, dementia research registries have been developed in Asia and Europe. The Clinical Research Center for Dementia of South Korea Study (CREDOS) initiated a longitudinal dementia registry in 2005 with a focus on specific dementia subtypes including AD to collect data on demographic and patient characteristics and to assess disease prevalence (Park et al., 2011; Hye Choi et al., 2012; Kim et al., 2014)The Prospective Dementia Registry Austria (PRODEM) was established in 2008 as a longitudinal cohort of AD patients to collect data on clinical evaluation, magnetic resonance (MR) imaging and diagnostic markers (Seiler et al., 2012). Some registries have used an epidemiological surveillance model where specific populations are maintained under surveillance to provide standardized data. For example, the Registry of Dementias of Girona (ReDeGi) was set up in 2007 in Spain to record all new cases of dementia in the region of Girona and provide information about the demographic and clinical characteristics of dementia patients in the region (Garre-Olmo et al., 2009). The quality-of-care registries are among the most successful registry types (Hopper, 2017; Krysinska et al., 2017). The Swedish Dementia Registry (SveDem) is a national, online dementia registry that was established in 2007 to evaluate the quality of patient care and the adherence to national guidelines (Fereshtehnejad et al., 2015; Religa et al., 2015). SveDem includes more than 74,000 registered patients as of 2017 and collects data about diagnostic work-up and treatment. Quality of care registries are extremely beneficial as they focus on improving patients’ quality of lives which is the reason of the current shift toward creating this type of registries. The availability of common patients’ data that are usually collected in these types of quality-of-care registries makes it possible to link the registry with other patient or disease registries in the region. Using multiple data sources for a patient is tremendously valuable in finding the association between the disease and other comorbidities or risk factors. SveDem, for example, was merged with the Swedish Heart Failure Registry (RiksSvikt) (Cermakova et al., 2015), as well as the Swedish stroke registry (Riksstroke) (Zupanic et al., 2020). Many studies have analyzed data from these registries together to provide more insights concluded from these large sets of data.

The feasibility of creating new dementia registries is being explored in several countries. Hopper et al., assessed the feasibility of creating a national dementia registry for Ireland, discussed the benefits, anticipated outcome, most suitable strategies for constructing and managing the registry, and the most effective registry structure needed (Hopper, 2017). Most recently, a multi-partner project was initiated by the Latin American and Caribbean Consortium on Dementia (LAC-CD) to expand dementia research in the participating regions. The consortium’s objective is to collect genetic, neuroimaging and behavioral data to improve dementia diagnosis and help developing new interventions that benefit the diverse populations (Projects – LAC-CD, 2020).

Although many registries were already established and published studies based on their data, yet many of them still face some limitations. One of the main restraints in any registry is the minimal set of data that can be included. For example, quality of care registries focusses on patients’ history and treatment while lacking many diagnostic data including imaging and neurological tests which might hinders some areas of research. However, prioritizing the most essential set of data to be included in the registry while excluding the less important points is a major step in the planning of a registry which guarantees its success. Creating a registry that include everything about a patient is extremely difficult considering the availability of funds, as well as the sustainability of registries (Newton and Garner, 2002). Hence, a registry board should be cautious regarding which data should be included to be benefit the registry and achieve its objectives.

Literature Search and Data Collection

We performed a rapid literature search to identify the best-known dementia registries with high publication output to be included in the study. SveDem, NACC, ReDeGi, CREDOS, and PRODEM were selected. We then performed a comprehensive literature search to find the peer-reviewed papers that were based on the data of any of the selected registries. All the collected studies were categorized to develop common themes and sub-themes. Finally, the studies that did not fit any of the themes were filtered and we presented the data as how each of the different areas or themes benefited from the analysis of data provided by dementia registries.

Registries Outcomes on Quantifying the Disease: Incidence, Prevalence, and Mortality

Studying the prevalence and incidence of each dementia subtype in a specific region, as well as the associated sociodemographic risk factors is crucial for effective resource utilization and disease management. In addition, comparing dementia prevalence and risk factors across regions and countries will help determine if there are specific population-related risk factors that increase the disease incidence in different countries or regions.

Disease Incidence and Patient Characteristics

The ReDeGi registry in Spain has been facilitating studies that estimate the incidence of dementia in the population (Table 1). The validity of the registry data and the benefits of epidemiological surveillance in the specific defined geographical area that the registry covers have been reported (Garre-Olmo et al., 2009; Calvó-Perxas et al., 2012b). AD was the most frequent dementia subtype among the cases and the onset of symptoms before diagnosis was estimated to be 2.4 years. Disease risk factors included family history of dementia, history of depression and high blood pressure (Garre-Olmo et al., 2009). Another study used ReDeGi data to compare the characteristics of newly diagnosed cases of early onset dementia (EOD) and late-onset dementia (LOD) (N = 2083) (Garre-Olmo et al., 2010) using the traditional cutoff that define EOD as being diagnosed with an age at onset of less than 65 years old (Mendez, 2006). The incidence of dementia between the age group (50–64 years old) was significantly higher than the younger age (group 30–49 years old) and doubled with every 5-years age increase. AD was the most frequent subtype of EOD followed by secondary dementia (a form of dementia related a pre-existing mental or physical condition), vascular dementia (VaD) and then frontotemporal dementia (FTD) (Garre-Olmo et al., 2010).

Although AD and VaD are highly frequent, the clinical characteristics of the uncommon dementia subtypes were also investigated as they are considered a challenge to diagnose. Data from ReDeGi showed that these less common subtypes were more frequent in people aged over 65 years. Non-AD neurodegenerative diseases represented the highest incidence rate among patients, with dementia with Lewy body (DLB) and Parkinson’s disease dementia (PDD) being the most frequent subtypes. Demographic and clinical characteristics also differed, for example, non-AD neurodegenerative dementia and dementia due to multiple causes occurred mainly in men and those that were older. In contrast, women were predominantly represented in those with dementia associated with a mental health disorder, as a higher number of women had a history of depression or were referred from mental health service units (Calvó-Perxas et al., 2019).

Environmental factors were also found to affect the clinical manifestations of the disease. The cost and accessibility to healthcare services, as well as aging among the population were major contributors to the incidence rate of dementia. Clustering cities into aged or young regions according to the number of older people living in the city showed that the incidence rate of dementia diagnosis is lower in the aged cities. This phenomenon may be partly explained by the adaptation of the environment docility hypothesis in that the surrounding environment may influence an individual living in young region to look for help and hence get an early diagnosis. In contrast, living in aging municipalities, there is less cognitive pressure on performing daily activities (Morgan et al., 1984). As the required cognitive functions in performing everyday activities are lower, symptoms of dementia will not become evident and fewer cases of dementia are diagnosed (Calvó-Perxas et al., 2015). All in all, the ReDeGi registry provided researchers with a significant amount of data on dementia patients that allowed them to determine the incidence of dementia in the population, the most frequent subtypes, the patients’ characteristics, and the environmental factors contributing to these characteristics (Table 1).

The Swedish registry, SveDem, has had a major role in facilitating dementia epidemiological studies as well. Religa et al. (2012) examined the differences in age and gender among SveDem dementia patients (N = 6937) and showed that age and severity of dementia predict the number of diagnostic tests that patients can complete. Diagnostic workups were significantly higher among younger patients who were able to complete more tests and had higher MMSE scores in comparison to lower diagnostic workups in older individuals who also had lower MMSE scores. Religa et al. (2012) also reported some gender differences in workup as men were more likely to complete higher number of diagnostic tests, in comparison to females. Taken together, the adequate number of dementia diagnostic tests should be adapted based on the age and dementia severity of the participants. In other words, using a fewer number of tests will help older individuals complete the diagnostic workup, and thus provide a more accurate diagnosis (Religa et al., 2012). In contrast, two other groups of DLB and PDD patients did not show any differences except a significant lower age of disease-onset and less cognitive impairment in the PDD than in DLB group (Fereshtehnejad et al., 2013, 2018). Additionally, the diagnostic process and disease management were investigated in rural and urban areas of Sweden as the geographical variations may represent important socio-environment contributors to dementia incidence and etiology. Roheger et al. (2019) used SveDem data to demonstrate that the dementia diagnostic procedures such as the basic examination, MMSE test, blood analysis and neuroimaging were, surprisingly more complete among patients living in rural than urban or intermediate areas. They suggested that their results might be due to sampling bias or that the patients living in rural areas are more likely to be registered in SveDem and therefore have a complete diagnostic work-up. Gender was also a factor as male patients received more complete diagnosis than women did (Roheger et al., 2019). This type of study should be considered for future improvements of disease management by avoiding inequalities among rural and urban areas and ensure the inclusion of complete workup tests for all cases.

Moreover, a recent study compared the data of two dementia registries, SveDem and ReDeGi to determine the differences in subtypes frequency, demographics, and clinical manifestations. The results showed significant differences between the two cohorts in MMSE test scores and the frequency of dementia subtype among the registry participants. However, there was no significant difference in age and gender of the participants in both cohorts. SveDem cases had higher MMSE scores at diagnosis than ReDeGi cases. AD was the most frequent subtype although its percentage was higher in ReDeGi cases. On the other hand, VaD and mixed dementia accounted for higher percentages in SveDem cases. Differences in medication profiles at the time of diagnosis were also identified as patients from ReDeGi consumed higher amounts of antipsychotics than SveDem patients. The differences in results could be explained by the variability of the genetic profiles of the two populations, differences between the specialists who performed the diagnosis or by the differences in diagnostic assessment. However, additional data regarding the education level of registered cases, the severity of dementia symptoms and the length of their treatment would be helpful to fully understand the cause of these differences (Garre-Olmo et al., 2016).

The use of registry data from SveDem and ReDeGi is greatly impacting our understanding of the disease prevalence and the differences in patient characteristics through providing data from the real world (Table 1). Understanding these differences may help improve the disease prediction algorithms for more precise patient handling. However, relying on these data should be done cautiously as registries data usually have the limitation of inclusiveness. Most registries depend only on patients registered in specific hospitals or memory clinics neglecting other private or emergency geriatric centers, and more substantially the undiagnosed patients in the population. Yet, having a source of evidence that enables the estimation of epidemiological features of such an underdiagnosed disease based on real-world data is extremely necessary. These real-world data will also help the policymakers in taking their decisions of services improvement, resources and budget allocation based on real evidence.

The Risk of Mortality

Life expectancy is severely affected by dementia. Patient survival (i.e., how many years the patient will live after diagnosis) and years of life lost after dementia diagnosis (i.e., years representing premature death) should be considered as they differ depending on the type of dementia, gender, cognitive level and several other factors (Ganguli et al., 2005; Brodaty et al., 2012; Koller et al., 2012). Accordingly, it is crucial to have data on mortality risk among dementia patients to determine the appropriate resources and services required for patients and their families (Garcia-Ptacek et al., 2014a). Numerous studies have investigated the risk of mortality in dementia patients although the availability of large cohorts or databases is rare. Most of the studies have focused on AD and VaD with little information about other dementia subtypes (Fitzpatrick et al., 2005). Furthermore, the factors that influence the risk of mortality might differ according to diagnosis (Clarke et al., 1995; Rountree et al., 2012). For these reasons, further studies that explore dementia mortality risk using large cohorts and registry databases are essential to obtain more valuable information on managing the disease (Lönnroos et al., 2013).

The establishment of SveDem offered a great opportunity to address the limitations of mortality studies by examining a very large cohort of dementia patients with a wide variety of dementia subtypes and with all their records available on the web (Garcia-Ptacek et al., 2014a; Table 2). A comparison of mortality risk among the most frequent dementia types in SveDem patients showed that VaD corresponds with the highest crude mortality rate while FTD is associated with the highest adjusted mortality risk. In contrast, the risk was lowest in AD patients. Higher age, male gender, institutionalization, lower cognition as scored by the MMSE test and a greater number of consumed medications at diagnosis were all factors that corresponded with higher risk of mortality (Garcia-Ptacek et al., 2014a). On the other hand, registry-based studies reported that body mass index (BMI) has a different role as the higher BMI the patient has at the time of dementia diagnosis, the lower risk of mortality the patient had. These results remained true for male patients up to (25–29.9 kg/m²) compared to females only up to (24.9 kg/m²) which might be explained by the social and biological differences between males and females (García-Ptacek et al., 2014b; Jang et al., 2015).

Investigating the actual cause of death has revealed that dementia is usually underreported as the cause of death irrespective of the dementia subtype. AD patients, unlike other dementias, had lower all-cause risk of death. Cardiovascular diseases were the most common cause of death among dementia patients especially those with VaD, while respiratory diseases accounted for more death cases among patients with dementia with Lewy bodies (DLB) (Garcia-Ptacek et al., 2016). In addition, there was no significant difference between DLB and PDD in terms of mortality risk (Fereshtehnejad et al., 2018).

Thus, dementia registries have enabled us to study the causes of mortality among large cohorts of dementia patients to better understand and predict mortality risk (Table 2). Predicting the risk of death in each dementia group or subtype might help decrease the mortality rates among dementia patients through providing each group of patients with the most suitable management plan to treat the comorbidities and avoid the risk of death, as well as improving the quality of their lives.

Impact of Registries on Disease Management

Diagnostic Procedures and Risk Factors

The early and accurate diagnosis of dementia is essential for better disease monitoring and cost reduction in terms of care. However, in real life practice, the assessment of dementia and AD always occur after the symptoms have already developed and the disease has declared itself. Until now, there have been no widely used biomarkers that can facilitate dementia diagnosis and predict the disease before symptoms become apparent. Accordingly, exploring the factors that are associated with dementia in large cohorts of patients is crucial to identify the risk factors and understand mechanisms to modify these factors or diagnose the disease in early stages. Dementia registries have facilitated the research in the area of diagnostics and risk factors (Table 3). Research studies based on NACC registry data suggest that different modifiable factors such as sleep disturbance, depression and traumatic brain injury, as well as the non-modifiable factors including genetic biomarkers as apolipoprotein E (APOE) or abnormal aggregation of proteins like alpha synuclein and TDP-43 as potential risks of dementia and AD development (Burke et al., 2016; Bayram et al., 2019). PRODEM data analysis showed that quantitative EEG markers can also be considered as electro-psychological markers that relate to dementia and AD diseases although they remain research tools and are not used clinically (Fruehwirt et al., 2019). In addition, Schaffert et al. (2020) used NACC registry data to investigate six modifiable and non-modifiable risk factors as contributors to early dementia onset by examining different autopsy confirmed samples of AD, mixed AD and LBD, and pure LBD. APOE ε4 allele and male sex increased the risk of early onset by approximately 2 to 3 years in AD and mixed AD + LBD, while in pure LBD, depression and high education predicted a 5.5-year earlier onset of dementia (Schaffert et al., 2020).

Genetic Biomarkers and Non-modifiable Risk Factors

Several studies have investigated the mechanism and associated risk of each genotype of APOE (Genin et al., 2011; Liu et al., 2013), but the major limiting factor of these studies was the small sample size that cannot detect or confirm the association of each genotype with other risk factors. There is a need to study larger populations for more powerful and informative analyses.

The NACC data has greatly contributed to improving the research studies investigating the presentation of AD symptoms among a United States population cohort, as well as identifying the potential genetic biomarkers that are associated with dementia and their relevance to the other risk factors of the disease (Table 3). It is increasingly recognized that AD dementia does not always begin with memory complaints, as less typical non-memory symptoms like language problems, visuospatial dysfunction, dyspraxia, and others can present as well (Jacobs et al., 1994; Koedam et al., 2010). A study of the NACC cohort reported that patients, especially those with younger onset, experience non-memory cognitive or behavioral symptoms first in contrast to older patients who usually experience memory decline at their first presenting symptoms (Barnes et al., 2015).

Examining the influence of APOE ε4 on the development of non-memory cognitive symptoms such as language, visuospatial function, judgment, and attention symptoms in the NACC has shown that it has little influence on the development of cognitive symptoms. Accordingly, the effect of APOE happens early in the disease before the occurrence of cognitive symptoms while other genes are responsible for developing the non-memory symptoms (Blenkinsop et al., 2020). Another study used NACC data, as well to compare the proportion of APOE ε4 genotype in patients with memory or amnestic symptoms vs. non-memory or aphasic symptoms while controlling sex and age at symptom of onset and confirming data with a group of autopsy samples (Weintraub et al., 2020). The proportion of APOE ε4 was higher in patients with amnestic symptoms than in the aphasic patients which may mean that APOE ε4 is a risk factor that selectively increases memory symptoms (Weintraub et al., 2020). In addition, the risk of the APOE ε2ε4 was unclear as it encompasses both the toxic ε4 and protective ε2 copies (Ren et al., 2020). The role of APOE ε2ε4 in developing AD dementia or mild cognitive impairment (MCI) was examined in non-Latino white patients to control for the influence of ethnic group. APOE ε2ε4 was associated with an increased risk of AD and MCI similar to APOE ε3ε4 and ε4ε4 genotypes (Ren et al., 2020). Studying the effect of APOE ε4 genotype and age of onset on the progression of AD, data from NACC indicated that carrying APOE ε4 genotype influences the progression to MCI or AD in all ages especially in the older groups (70–75). These results will help tailoring the therapeutic interventions, when available, based on the genetic data and age of patient (Bonham et al., 2016).

Moreover, CREDOS data was also very useful in studying APOE prevalence in Korean dementia patients. Hong et al. (2011) compared the frequency of APOE ε4 and the difference in clinical features between AD and SIVD patients, with and without severe white matter hyperintensities (WMH). APOE ε4 was more prevalent in AD than SIVD patients while the frequency was not affected by the presence or absence of WMH (Hong et al., 2011). However, severe WMH and APOE ε4 have an interactive effect on memory cognitive function (Son et al., 2012; Table 3). Thus, the studies on genetic factors associated with dementia, particularly APOE genotype, were facilitated by the availability of registries data. Further research on this area would be important to better understand the disease pathogenesis and determine the genetic risks which might help with early disease diagnosis.

Modifiable Risk Factors

There is an increasing emphasis on identifying modifiable risk factors of dementia in order to develop better strategies to prevent the disease before symptoms can develop. Researchers have investigated a number of modifiable risks that are associated with dementia by analyzing data available in dementia registries (Table 3).

History of traumatic brain injury (TBI) is, for instance, an important risk factor associated with dementia (Sivanandam and Thakur, 2012). Mendez et al. (2015) used the NACC database to investigate whether TBI is associated with early onset AD (EOAD) and found that the prevalence of TBI in EOAD patients was higher than LOAD which suggests that TBI may be a specific risk for early onset disease (Mendez et al., 2015). Another study used NACC data and reported that TBI can lead to AD misdiagnosis and reduce the accuracy of diagnosis through an increased risk of false positive results which can have serious implications for patient treatment (Pradeep et al., 2020).

Sleep disturbance and depression are considered as potential modifiable AD risk factors, as well (Marques et al., 2010; Pistacchi et al., 2014). NACC data investigation showed that sleep disturbance, depression as well as APOE genotype are associated with subsequent diagnosis of AD dementia (Burke et al., 2016). Overall, mental health disorders are among the strong predictors of AD diagnosis, so enhancing individuals’ mental health might decrease the risk of AD developing later on (Xu J. et al., 2020). Further exploration of registries data would help identifying more risk factors and how they increase the risk of dementia and hence, determining the most appropriate strategies to avoid them.

Electro Psychological Markers

Quantitative electroencephalogram (qEEG) is a low cost, non-invasive tool that has potential to differentiate patients with AD from normal controls (Dauwels et al., 2010; Drago et al., 2011). Investigating qEEG analysis and cognitive parameters among large cohorts of dementia patients is essential to evaluate whether qEEG can be used as a diagnostic marker for AD (Klimesch, 1999; Garn et al., 2014b).

Prospective Dementia Registry Austria was a valuable source of data that facilitated qEEG research. Garn et al. (2015) reported that face-name encoding with eyes open was better than resting state and strongely correlated to MMSE scores. Early to moderate stages of AD are associated with qEEG changes that can be determined using signal processing (Garn et al., 2014b). Dauwels et al., studied various synchrony measures for AD diagnosis with EEG data and were able to identify the two synchrony measures that can distinguish MCI patients from control patients (Dauwels et al., 2010). In addition, qEEG markers were shown to be closely related to AD severity especially in patients with MMSE scores between 15 and 26 (Garn et al., 2014a,2015; Waser et al., 2014, 2016; Coronel et al., 2017). Moreover, PRODEM data showed that qEEG can be used to predict rapid cognitive decline in AD patients (Reyes-Coronel et al., 2016). Taking altogether, qEEG markers have potential as diagnostic markers for dementia but further investigations of their accuracy are required. Using data from different disease registries to study qEEG markers and their relevance to AD diagnosis may help establish if this tool could be used as part of the standard diagnostic procedures for AD (Table 3).

Overall, the existing dementia registries represent a valuable tool for studying the known risk factors of the disease, as well as, identifying new risk factors and markers that may help improve the accuracy of diagnostic procedures of the disease (Table 3). Non-modifiable risk factors including the genetic attributes as well as the modifiable risk factors such as sleep disturbance and mental health status have been investigated by using large baseline patient data sets as well as the longitudinal follow-ups in some registries. Therefore, expanding the registry data to include more patient history is essential to allow the determination of more associated risk factors.

Registries and Drug Treatments

Dementia patients usually receive multiple drug treatments prior to and post-diagnosis. Centrally active drugs that are frequently prescribed to dementia patients can be mainly divided into two groups: anti-dementia drugs and drugs that treat behavioral and psychological symptoms of dementia. The first group includes acetylcholinesterase inhibitors (AChEIs) that are used in mild to moderate cases and memantine, and an NMDA receptor antagonist that is used in moderate to severe cases. Antipsychotics, anxiolytics, hypnotics, antidepressants, and sedatives are all used to handle different dementia associated behavioral symptoms (Bond et al., 2012; Turró-Garriga et al., 2015). In addition, dementia patients usually have comorbidities such as hypertension, diabetes mellitus or dyslipidemia, among others. Thus, dementia patients are frequently prescribed many other medications besides dementia-specific drugs (Andersen et al., 2011). Studying the effect of these treatments on large cohorts of dementia patients is crucial to determine the best management strategy of the disease and avoid the adverse side effects of polypharmacy.

Numerous studies have analyzed the data available on SveDem registry to explore the impact of medication consumption on dementia patients, as well as to compare the use of drugs among different disease subtypes (Table 4). These studies have shown that anti-dementia drugs are frequently used among all patients. In patients with DLB, the use of antipsychotics was significant, which is a concern due to the potential for severe side effects (Johnell et al., 2013). Women were more likely to be treated with cholinesterase inhibitors (ChEIs) than men (Johnell et al., 2013). Additionally, patients with early onset (EOAD) received ChEIs more than patients with late age of onset (LOAD), although they were generally receiving fewer overall drugs (Eriksson, 2014; Fereshtehnejad et al., 2014b). Patients on ChEIs were less likely to receive antipsychotics and anxiolytics than those not taking ChEIs (Fereshtehnejad et al., 2014b). However, the cautious use of medications should be considered as some medications that are used for treating dementia symptoms or even for treating other co-morbidities are xerostomic and usually cause hyposalivation and dry mouth which can increase the risk of oral complications, tooth extraction or loss (Lexomboon et al., 2018).

The ReDeGi registers data have also been used to investigate of the use of pharmaceutical medications in dementia. A study by López-Pousa et al. (2012) focused on studying patients with non-AD dementia (n-ADD) subtypes in terms of clinical data and patterns of prescribing. They reported that the use of anti-dementia medications including ChEIs was very frequent among patients with n-ADD although those pharmaceuticals are not effective for n-ADD according to the guidelines (López-Pousa et al., 2012; O’Brien et al., 2017). Age also played a role in ChEIs use as with advances in age, there was more likelihood that the patient would be on memantine and ChEIs rather than ChEIs alone (Calvó-Perxas et al., 2017). Additionally, atypical antipsychotics were extensively used in dementia patients to treat their behavioral and psychological symptoms despite the increased risk of adverse effects (Calvó-Perxas et al., 2012a,2014). Besides the risk of adverse effects, higher pharmaceutical use increases the costs of dementia disease management (Turró-Garriga et al., 2015). Accordingly, the risk-benefit ratio should be considered prior to prescribing treatments to dementia patients. Furthermore, guidelines should be improved to recommend the most effective treatment strategy for severe dementia patients (Turró-Garriga et al., 2017).

As mentioned earlier, the consumption of medication at the time of diagnosis is associated with higher risk of mortality (Garcia-Ptacek et al., 2014a,2016; García-Ptacek et al., 2014b). A wide range of medications are prescribed to dementia patients to treat behavioral symptoms, but they can be associated with serious side effects. Several studies assessed the effectiveness of the commonly used medications in dementia and their influence on the risk of mortality (Calvó-Perxas et al., 2013; Enache et al., 2016; Tan et al., 2018a,b; Schwertner et al., 2019). Although antidepressants are commonly used to treat dementia patients, they may neither increase nor decrease the risk of mortality. However, it was shown that the use of antidepressants during prodromal stages and prior to dementia diagnosis for 3 consecutive years is associated with decreased risk of mortality especially in AD patients (Enache et al., 2016).

Medications with anticholinergic properties are commonly used in dementia patients (Roe et al., 2002). Turró-Garriga et al., described the prevalence of anticholinergic exposure in dementia patients to be 36.3–69% determined based on the severity of the disease (Turró-Garriga et al., 2018). However, the aggregated effects of anticholinergic medicines, known as anticholinergic burden, have significant adverse effects on cognitive and physical functions of patients (Fox et al., 2014a; Gray et al., 2015). Tan et al., investigated the effect of anticholinergic burden on stroke outcomes and mortality risk in dementia patients. They reported that an increased risk of stroke is usually associated with the use of anticholinergic medicines and hence it increases the risk of mortality (Tan et al., 2018a). In contrast, the use of ChEIs in dementia and AD patients was associated with lower risk of stroke and death (Tan et al., 2018b). Moreover, the impact of antipsychotics use on mortality risk was also explored. The use of both typical and atypical antipsychotic drugs was associated with higher mortality risk in patients with dementia (Schwertner et al., 2019).

Disease registries have enabled clinicians and researchers to gain insights into the commonly used medications and their effectiveness and adverse effects in managing dementia. Using SveDem (Xu et al., 2021) found that cholinesterase inhibitors use was associated with higher memory over time (as measured by MMSE) and lower death compared to patients not using Cholinesterase inhibitors. Similarly, using SveDem (Secnik et al., 2020a), found that cholinesterase inhibitors use was associated with reduced mortality. One study found that cholinesterase inhibitors use reduces neurological and functional problems in pre-stroke dementia (Wakisaka et al., 2021). By using different registries, cholinesterase inhibitors were found to be associated with better cognition in patients with vascular dementia (Battle et al., 2021).

However, more data on the medications used pre- and post- dementia diagnosis should be considered when registering patients. The duration of treatment and the actual doses are also important to consider. Having an integrated patient registry that contains all the information about treatment history will help with studying the effectiveness of different anti-dementia medications and predicting the adverse effects that could arise when using multiple medications and thereby help improve the current treatment approaches and allow for better disease management. Identifying more precised treatment approaches will also lead to enhanced patients’ quality of life which is the most important objective of all registry initiatives as well, as the studies build on them.

Dementia Registries Advance Our Knowledge of the Disease

Association of Dementia With Other Diseases

To date, little attention has been paid to research on the specific healthcare needs of dementia patients. Dementia is more common in people with older ages who often have other medical problems or comorbidities (Fox et al., 2014b). Several comorbidities including diabetes, cardiac diseases, pulmonary diseases, musculoskeletal disorders, mental disorders and others have been reported commonly in dementia patients and shown to reduce their quality of life (Schubert et al., 2006; Martín-García et al., 2013). In addition, the elimination of some of these comorbidities including diabetes, depression and hypertension may help reduce the percentage of new cases diagnosed with dementia (Livingston et al., 2017). Accordingly, early prediction, diagnosis and management of new conditions that are associated with dementia patients may help decrease the severity of the disease and improving their quality of life (Marengoni et al., 2009; Thorpe et al., 2012). The availability of data recorded for patients with dementia in the several international registries has allowed researchers to investigate the risk of other diseases that may be associated with dementia and to create comorbidity profiles for the different dementia subtypes (Fereshtehnejad et al., 2014a; Table 5).

The relationship between hypercholesterolemia (HC) and AD was among the comorbidities that warranted investigation as HC was shown to accelerate AD pathology in animal studies (Xu C. et al., 2020). Using neuropathological and clinical data of the large national sample with autopsies from NACC, a group of researchers were able to investigate the association of hypercholesterolemia (HC) with AD. They suggested that the severity of AD disease was increased with the existence of HC. The association of the two diseases was significant even when the model was adjusted to control the ApoE genotype (Xu C. et al., 2020). In addition, data from NACC helped to investigate the association between controlling systolic blood pressure and the risk of AD. Survival analyses in older adults with treated hypertension and comorbid depression showed that the intensive control of systolic blood pressure was associated with risk of AD. The actual reasons are not yet fully understood, however, the cautious management of hypertension in these vulnerable groups will be needed (Yeung et al., 2020).

Diabetes Mellitus was also one of the comorbidities that needed investigation as several studies suggested its association with the risk of dementia and AD (Lu et al., 2009; Mittal and Katare, 2016). Data from SveDem was used in a registry-based study to investigate large cohort of dementia patients with diabetes and its impact on their clinical characteristics and treatment. The study reported that diabetic patients were younger than control patients when diagnosed with dementia and they received less dementia medications (Secnik et al., 2017). In addition, researchers initiated an open-cohort study to evaluate the effectiveness of some dementia medications including ChEIs in patients with diabetes. They reported that patients with diabetes and dementia or AD had reduced mortality risk when receiving ChEIs, particularly donepezil and galantamine (Secnik et al., 2020a). On the other hand, Scenik et al., examined the pharmacological changes in the treatment of diabetes in patients with dementia. They indicated that dementia patients were less likely to receive new diabetes medications and they had higher insulin dispensation ratio than non-dementia controls (Secnik et al., 2020b). Reviewing NACC data showed also that diabetes is associated with accelerated cognitive decline in patients with APOE2 and APOE3 genotypes but not APOE4 carriers (Shinohara et al., 2020). Thus, dementia registries data have contributed to our understanding of the relation between dementia and diabetes and the management of patients with both comorbidities. Further research will be crucial to determine the most appropriate treatment plan to increase patients’ survival and decrease the severity of cognitive impairment (Secnik et al., 2017). Understanding the mechanisms by which diabetes is associated with dementia will help, as well as understanding new management approaches.

Cognitive impairment frequently occurs with cardiovascular diseases (CVD) and heart failure (HF) but the underlying mechanisms remain unclear. Various studies reported that cognitive impairment is a risk factor of CVD which make CVD and HF patients are at increased risk of developing dementia or AD (Angermann et al., 2012; Roher, 2015). To investigate the relationship between HF and dementia, researchers used SveDem data to study the difference in prognosis in patients with HF and dementia, assess the proportion of different dementia subtypes among HF patients and describe their clinical characteristics. They found that vascular dementia was the most common subtype associated with HF with no associated survival in either dementia or HF patients (Cermakova et al., 2015). SveDem data was also used to study patients with acute myocardial infarction (AMI) and dementia, and whether using invasive procedures in their management would affect their survival. Using invasive procedures can enhance the survival of patients with dementia and AMI (Cermakova et al., 2017). Moreover, Subic et al., studied the benefits and complications associated with anticoagulant therapy in patients with dementia and atrial fibrillation (AF). Patients on warfarin had decreased risk of developing ischemic stroke unlike those on antiplatelets which increased Ischemic Stroke risk. Using warfarin was associated with lower mortality rate in dementia patients which indicates the benefits of warfarin on stroke prevention (Subic et al., 2018a).

Cerebrovascular disease usually coexists with dementia and dementia patients are at increased risk of developing strokes which increases their disability and dependency (Hay et al., 2017; Subic et al., 2017). Accordingly, managing dementia patients become more challenging when acute stroke exists (Saposnik et al., 2011). Previous studies proposed that dementia negatively affects survival and outcomes of stroke, but little attention was given to the management of patients with dementia and stroke (Saposnik et al., 2011, 2012). Data from SveDem registry allowed researchers to investigate the association between dementia and stroke, and the provided care plans (Table 5). Gracia-Ptacek et al., investigated prestroke mobility dependency and its association with dementia and post-stroke outcomes. They demonstrated that dementia patients were more likely to have impaired functionality and dependency prior to stroke. After stroke, dementia patients had a higher likelihood of developing poor mobility, disability and accordingly increased residential assistance and mortality (Garcia-Ptacek et al., 2018). Investigating this higher mortality rate in dementia patients revealed that most of the dementia patients who had ischemic stroke in their death certificates were not registered in the Swedish stroke registry (Riksstroke), which makes the accuracy of these death certificates questionable (Subic et al., 2018b). Zupanic et al., studied the hospital management of acute ischemic stroke patients with dementia. They reported that there was no difference in most of the aspects of stroke care between patients with or without dementia as all had equal access to stroke unit care (Zupanic et al., 2018). SveDem data was used, as well, to study the treatment plans of secondary stroke prevention to decrease cognitive decline by comparing between patients with and without dementia. The study reported that patients with dementia were more likely to receive antiplatelets post-stroke while they were less likely to receive anticoagulants, statins and blood pressure lowering medications (Zupanic et al., 2020). In addition, the administration of intravenous thrombolysis showed no significant difference among patients with or without dementia (Zupanic et al., 2017). These results may represent a new target to improve the quality of care of dementia patients.

Epilepsy has also been examined to investigate whether its risk increases with dementia. Examining SveDem large cohorts, Zelano et al., found that the risk of subsequent epilepsy increases with dementia (Zelano et al., 2020). When studying the risk of epilepsy diagnosis after the first unprovoked seizure in patients with dementia, researchers suggested that epilepsy cannot be diagnosed after the first seizure only on the basis that a patient has dementia (Mahamud et al., 2020). Rather, researchers should investigate how to predict the risk of epilepsy in dementia patients (Mahamud et al., 2020). More studies are needed to understand the exact mechanisms for the association between epilepsy and dementia in order to prevent the occurrence of epilepsy in dementia patients and enhance its management.

In conclusion, the data available in different dementia registries helped us advancing our knowledge of the disease and how it associated with different medical comorbidities. Investigating the clinical characteristics of large cohorts of patients will allow the determination of the most appropriate ways to manage dementia patients with comorbidities, with the ultimate goal of improving the quality of life of dementia patients.

Conclusion

Dementia registries have significantly improved our knowledge of dementia and have contributed to enhancing dementia research. The availability of large data sets has greatly impacted on clinical practice and will help redirect government policies as well as the healthcare services to better reflect patient needs, with clinical and economical benefit. The growth in registries data has enabled researchers to study different cohorts to determine the risk factors of the disease, prevalence and identify new disease markers for earlier diagnosis and better management. In addition, an improved understanding of the socio-demographic and socioeconomic factors that can influence patient outcome will help lead to more precision and targeted patient centered treatment.

Many national and international dementia registries have improved our knowledge of the disease through the use of observational, cross-sectional and longitudinal data. SveDem and ReDeGi, for instance, significantly contributed to our knowledge on the disease prevalence and differences in patients’ characteristics which will be important to develop new algorithms to predict the disease. In addition, greater knowledge of mortality risks will help provide patients with the appropriate services that can improve their survival. NACC, PRODEM, and CREDOS also contributed information regarding the modifiable and non-modifiable risk factors that are associated with dementia. Understanding the underlying mechanisms of how these risk factors contribute to the pathogenesis of dementia will be crucial to early diagnosis and new treatments for the disease.

Moreover, investigating patients’ outcomes with different treatment strategies for dementia patients with or without comorbidities will help determine the most appropriate management strategy for each case to improve the quality of their lives.

Given the benefits of dementia registries and their contribution to improved understanding of risk and outcomes, the development of dementia registries should be considered in all countries where such gaps exist. Harmonization efforts of dementia registries across countries should also be explored to determine whether risk and protective factors are the same in different countries and continents and to share learnings in how best to tackle the global challenge of dementia.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

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