Protocol
Abstract
Background: Understanding mild behavioral impairment, a relatively recent notion in neuropsychological studies, provides significant insights into early behavioral indicators of cognitive decline and predicts the onset of dementia in older adults. Although the importance of understanding mild behavioral impairment is acknowledged, comprehensive reviews of its correlates with older adults are limited.
Objective: This scoping review aims to identify the impact of mild behavioral impairment on health outcomes in older adults and the factors associated with mild behavioral impairment.
Methods: The review will adhere to the Joanna Briggs Institute’s methodological principles for scoping reviews. We will include studies focusing mainly on mild behavioral impairment in older adults, with the literature on this topic being limited to the period from 2003 to the present. Other clinical diagnoses, such as cognitive impairment, Parkinson disease, and multiple sclerosis, will not be included. We will use databases including PubMed (MEDLINE), CINAHL, Web of Science, Embase, PsycINFO, Cochrane, and Scopus for relevant articles published in English. Both gray literature and peer-reviewed articles will be considered during screening. Three independent reviewers will extract data using a predefined data extraction tool. Extracted data will be presented using tables, figures, and a narrative summary aligned with review questions, accompanied by an analysis of study characteristics and categorization of mild behavioral impairment correlates.
Results: The results will be presented as a descriptive summary, structured according to the associated factors related to mild behavioral impairment, and the health outcomes. Additionally, the data on study characteristics will be presented in tabular format. An exploratory search was conducted in July 2023 to establish a comprehensive search strategy, and iterative refinements to the scoping review protocol and formalization of methods were completed. A follow-up search is planned for May 2024, with the aim of submitting the findings for publication in peer-reviewed journals.
Conclusions: To our knowledge, this would be the first study to map the literature on the health-related factors and outcomes of mild behavioral impairment. The findings will support the development of interventions to prevent the occurrence of mild behavioral impairment and mitigate the negative outcomes of mild behavioral impairment.
International Registered Report Identifier (IRRID): DERR1-10.2196/60009
doi:10.2196/60009
Keywords
Introduction
As population aging continues to become an irreversible global trend, the prevalence of dementia is also expected to increase rapidly. The global prevalence of dementia in older adults is projected to double every 20 years, reaching 58 million in 2020, an anticipated 82 million in 2030, and 150 million in 2050 [
]. The financial cost of dementia was already substantial at US $ 818 billion in 2015 [ ]. However, the recent COVID-19 pandemic has amplified the escalating costs of dementia care [ ]. The economic impact of dementia extends beyond direct medical and social service expenses, such as treatment, medication, and social welfare, and encompasses indirect costs borne by caregivers and family members of older adults with dementia [ , ]. Caregivers often experience long-term stress, depression, anxiety, burnout, and physical health problems, which can limit their participation in economic activities, thereby amplifying the significant economic burden associated with dementia care [ , ]. The escalating health care burden presents a global social challenge that impacts not only the affected individuals but also families and communities, underscoring the urgent need for comprehensive strategies to address this pressing issue [ ].Although no cure for dementia currently exists, several studies have suggested that preventive interventions in the preclinical and prodromal stages can delay its onset and improve cognitive function by targeting modifiable risk factors [
, ]. The preclinical stage represents individuals who, despite not showing overt clinical signs of cognitive decline, have underlying dementia pathology. Meanwhile, those in the prodromal stage display evidence of clinical decline, demonstrated by subtle changes in cognition and short-term memory loss [ , ]. These stages have become focal points of recent research. Typically, the progression starts with normal cognition, transition into subjective cognitive decline (SCD)—a decrease in cognitive ability that is subjectively perceived compared to prior normal status but irrelevant to objective cognitive test results [ ]—and eventually evolves into mild cognitive impairment (MCI), a condition characterized by a noticeable decline in cognitive abilities that does not interfere with daily functioning but increases the risk of Alzheimer disease or other types of dementia [ - ]. This transitional state of MCI poses a relatively high risk of progression to dementia, with some studies highlighting an estimated annual progression rate of approximately 10% [ - ]. However, not all cases of MCI inevitably progress to dementia [ ]. The rate of return to normal cognition from MCI varies across studies, but one meta-analysis reports that approximately 24% of individuals with MCI revert to objectively normal cognition [ ].Recently, mild behavioral impairment (MBI), a neuropsychological syndrome that typically emerges later in life and can manifest across the entire predementia spectrum, has been introduced as a precursor to cognitive decline and dementia [
]. Prior to the development and implementation of preventive and supportive interventions for at-risk populations, it is essential to thoroughly understand MBI and its related factors that can influence multidimensional aspects of health in older adults.According to the latest diagnostic guidelines published by the Alzheimer’s Association International Society to Advance Alzheimer’s Research and Treatment, MBI is characterized by behavioral and personality changes persisting for at least 6 months from the initial onset [
]. These changes, including reduced motivation, impaired emotional regulation, deficiency in impulse control, and inappropriate social behavior, minimally impact interpersonal relationships and workplace performance [ ]. Evidence suggests that older adults with SCD who experience MBI are more likely to develop dementia [ ]. Moreover, when MBI is accompanied by functional deterioration in daily life, it can serve as a neuropsychiatric symptom and prognostic marker of dementia [ , ]. Therefore, exploring the health outcomes of MBI has significant implications for dementia prevention and prediction of its progression.Since the diagnostic criteria for MBI were first introduced in 2003 [
, ], MBI has been studied over the past two decades as a predictor and prognostic marker of cognitive impairment and dementia [ , ]. During this period, significant strides were made toward the conceptual understanding of MBI and the development of tailored diagnostic tools offering consistent and reliable means of assessing MBI, such as the Neuropsychiatric Inventory Questionnaire (NPI-Q) and the MBI Checklist [ - ]. The MBI Checklist was validated in comparison with the NPI-Q [ ]. Furthermore, diverse methodologies have been employed in MBI research, including family interviews [ ], neuropsychological tests [ ], and imaging and cerebrospinal fluid diagnostic tests to identify MBI [ ]. Several studies have also scrutinized differences in MBI manifestations according to sociodemographic characteristics [ , ] and have examined correlations between biomarkers [ ], specific diseases, and MBI [ ] as well as the impact of MBI on the progression from MCI to dementia [ , ].However, as MBI is a relatively recent neurobehavioral concept, the literature lacks a comprehensive review addressing the correlates of MBI in older adults, apart from one meta-analysis on pathological and genetic relationships with MBI prevalence [
]. Given the potential insights into predicting and preventing dementia and assessing the risk of transition to this condition, a thorough review of the physiological, psychological, and social factors associated with the development and progression of MBI, as well as their influence on the relationship between MBI and other health outcomes, is crucial. Therefore, this scoping review aims to provide an overview of MBI and its correlates among older adults. Mapping evidence of factors correlated with MBI will guide the development of targeted preventative and supportive interventions for at-risk populations, laying the groundwork for interventions to promote preventive measures and improve self-management. This will also provide valuable insights for health care providers, enabling them to facilitate awareness and early detection of MBI. This, in turn, can lead to improved patient care and health outcomes. Furthermore, it underscores the importance of addressing behavioral symptoms later in life, and it advocates for targeted patient-centered clinical intervention and nursing care for older adults. The specific research questions are as follows:- What are the health outcomes associated with MBI in older adults?
- What are the identified factors associated with MBI in older adults, and how have they been reported to be related to MBI?
- What are the research trends in MBI, and what are the limitations and knowledge gaps in the existing studies?
Methods
Study Design
To identify the impact of MBI on health outcomes in older adults and factors associated with MBI, we seek to conduct a scoping review, which is the most suitable method for mapping evidence on this topic. This review follows the Joanna Briggs Institute’s methodology for scoping reviews [
] and reports the results according to the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews) checklist [ ]. An exploratory search took place in July 2023 to construct the full search strategy, yielding preliminary results. An update is scheduled for May 2024.Ethical Considerations
As this is a review of published and gray literature, ethical approval from a human research committee is not required.
Search Methods
Sources of Evidence
This review will consider observational (including prospective and retrospective cohort studies, analytical cross-sectional studies, and case-control studies), experimental (including randomized and nonrandomized controlled trials), and qualitative studies for inclusion. We will include papers published in English from 2003 to date. Given that most previous research on MBI has been conducted in English, prioritizing English-language publications ensures consistency in terminology, which is critical for the search strategy and inclusion criteria and allows for interpreting and summarizing the impact of MBI on health outcomes accurately in accordance with international standards. Additionally, restricting the review to English-language publications minimizes the risk of variability and potential bias, allowing little impact on the overall integrity and conclusions of the review [
, ]. Books, editorials, commentaries, and letters will be excluded. However, we will include gray literature sources, such as reports, working papers, policy literature, government documents, and newsletters for a more comprehensive review.Search Strategy
The search strategy will adhere to the PRISMA-ScR checklist [
]. Joanna Briggs Institute’s 3-step search strategy will be followed to ensure a comprehensive search. First, we will search MEDLINE and CINAHL to identify keywords and indexing terms in the titles and abstracts of potential articles that will be included in the review. This initial search will inform the development of the final search strategy. Second, these identified keywords and indexing terms will be used to search all the included databases. In other words, terms from the titles and abstracts of relevant articles, along with the indexing terms used to describe these articles, will be used to develop a comprehensive search strategy for multiple databases, specifically PubMed (MEDLINE), CINAHL, Web of Science, Embase, PsycINFO, Cochrane, and Scopus. After establishing a search formula using the appropriate subject words and consistent keywords in each database, the search formulae will be reviewed by a professional librarian at the university’s medical library. Tables S1–S7 in present the search strategy for each database. Third, after conducting the search using the previous strategies, we will analyze the bibliographies of the studies selected after the final search to identify relevant papers that may not be captured during the initial search. Our search strategy encompasses peer-reviewed published literature as well as gray literature, including doctoral dissertations to ensure comprehensive coverage.Information Sources
The following databases will be searched: PubMed (MEDLINE), CINAHL, Web of Science, Embase, PsycINFO, Cochrane, and Scopus. During the search process, we may discover other potentially useful information sources and terms that will be incorporated into the review. To ensure completeness, we will contact the original authors of the studies to further clarify this information, if necessary. As scoping reviews primarily aim to map evidence rather than synthesize findings, we will not evaluate the methodological quality of the included sources of evidence.
Inclusion and Exclusion Criteria
Population or Participants
This scoping review will include studies on older adults in the preclinical or prodromal stages of the dementia continuum, encompassing normal stages of SCD or MCI. Due to varying age thresholds for older adults in different studies, our review will adopt a broad approach, incorporating all studies that classify their population as “older adults” based on each study’s criteria. The term “older” refers to a specific group of adults who are chronologically older within the larger population of adults. The term has been broadly defined to include all studies that focus on recruiting older adults based on their criteria, such as being 60 years and older. Furthermore, the definition of older adults varies among countries, as diverse age standards exist for defining this population, according to the World Health Organization [
]. The diagnostic criteria for SCD and MCI adhere to the criteria established in each study.Considering the challenges of identifying early SCD without solid empirical data, our search criteria will also encompass older adults who have not obtained a definitive diagnosis. This means including those diagnosed with normal cognition at the time of the study, essentially expanding our focus to include individuals on the threshold of cognitive decline. Studies on older individuals with other clinical diagnoses that can result in cognitive decline as one of its symptoms, such as dementia, Parkinson disease, or multiple sclerosis, will be excluded. However, to enhance the comprehensiveness of our review, we will include studies that conducted supplementary analyses, wherein patients with dementia were subsequently excluded, despite their initial inclusion within the subject groups.
Concept
MBI is the key concept in this review. We will include literature published from 2003 onwards, as the diagnostic criteria for MBI were first presented in 2003 in an academic journal [
, ].Context
To thoroughly investigate the research questions related to MBI, there will be no restrictions on the study contexts or settings. A wide range of contexts will be considered eligible, including acute care, long-term care, and community-based environments.
Study Selection
All identified citations will be collated and uploaded to EndNote 20 (Clarivate Analytics), and the duplicates will be removed following the search. The titles and abstracts will be screened by 3 independent reviewers to assess the inclusion criteria. Prior to embarking on source selection, pilot testing for the title and abstract screening will be undertaken to refine the inclusion/exclusion criteria and validate the reviewers’ screening process using a randomly selected sample of 50 titles and abstracts. Thereafter, the full texts of potentially relevant sources will be retrieved. The full texts of the selected articles will be assessed in detail against the inclusion criteria by 3 independent reviewers. This review will report the reasons for excluding sources that fail to meet the predetermined inclusion criteria. Any disagreements between the reviewers during any stage of the selection process will be resolved by involving an additional reviewer or through discussion. The final scoping review will include a comprehensive report on the search results and the process of study inclusion, along with a presentation of the findings using a flowchart based on PRISMA-ScR [
].Data Extraction
Three independent reviewers will utilize the data extraction tool, as presented in
. The extracted data will encompass specific participant details, concepts, contexts, study methods, and the main findings relevant to the review questions. The preliminary data extraction tool will be adjusted and refined throughout the data extraction process for each source, as required. These modifications will be documented in the final review. In the event of any discrepancies between the reviewers, we will resolve them through discussion or by consulting an additional reviewer. If necessary, the authors of the selected studies will be contacted to obtain any missing or supplementary data.Data Synthesis
The extracted data will be presented using tables and figures to address the review questions. Tables will be constructed to illustrate the classification of MBI correlates, with comprehensive descriptions of health outcomes (research question 1), related factors (research question 2), and critical assessment of research limitations (research question 3). Additionally, a narrative summary will discuss how the results correspond to the objectives and questions of the review. During the discussion of results, we will analyze the characteristics of the selected studies and categorize MBI correlates according to their subgroups. The methods for presenting the results may be further refined during the review process, with details provided in the final review.
Results
An exploratory search was conducted in July 2023, and a comprehensive search strategy was formulated based on the preliminary results. We reviewed studies on MCI and SCD in older adults in the exploratory search and recognized the difficulty in detecting early SCD without substantial empirical data in individuals diagnosed with normal cognition at the study’s inception. Therefore, as noted in the Methods section, we broadened our review scope to include studies of older adults across the spectrum from normal cognition to MCI, refining our search strategy with a librarian's assistance. Iterative refinements to the scoping review protocol and formalization of methods were completed. A subsequent search is scheduled for May 2024, with the objective of submitting the results for publication in peer-reviewed journals.
Discussion
Expected Findings
This study introduces a protocol outlining a scoping review designed to address specific research questions regarding the correlates of MBI. The main findings of the review will identify key physiological, psychological, and social factors associated with MBI in older adults. Previous research has largely focused on the prevalence or individual domains of MBI, but this review will fill a significant gap in the literature, providing a broader understanding of how various factors contribute to MBI and the diverse ways MBI can impact health outcomes; to the best of our knowledge, such a review has not yet been conducted.
Strengths and Limitations
Our review will provide a timely and valuable contribution, encompassing evidence from various fields and methodological approaches and focusing on the physiological, psychological, and social factors associated with MBI in older adults. Understanding these factors and their influence on the relationship between MBI and health outcomes is crucial for proposing preventive measures and improving self-management strategies for person-centered intervention. This review will also contribute to the development of targeted preventive and supportive interventions aimed at alleviating the influence of MBI on health outcomes in older adults. Since this review will comprehensively map the correlates of MBI rather than measuring effectiveness, it will not perform a quality appraisal. Additionally, since non-English literature will not be included, some relevant studies may be missed which will reduce the generalizability of the findings. However, to increase the identification of eligible studies, we selected seven databases, including databases for gray literature, and developed appropriate search strategies.
Conclusions
This study will provide significant insights into the health-related factors and outcomes of MBI. Finally, it will lay the groundwork for policy development, fostering a broader social understanding of MBI, which can be a crucial focal point for future interventions targeting the at-risk group for dementia. Our knowledge dissemination strategy will employ various approaches, including peer-reviewed journals, webinars, and conference presentations. Collaborating with national research networks will extend our reach and inform policy, practice, and research. Recognizing the necessity for detailed dissemination plans, we will enhance our strategy by outlining specific channels to share our findings with academic communities, policy makers, and practitioners.
Acknowledgments
This work was supported by a National Research Foundation of Korea (NRF) grant (NRF-2022R1C1C2003706) funded by the Korean government—Ministry of Science and ICT (Information and Communications Technology); the Basic Science Research Program through the NRF, funded by the Ministry of Education (NRF-2020R1A6A1A03041989); a 2023 faculty-student research grant from Yonsei University College of Nursing (No 6-2023-0045); and the Brain Korea 21 FOUR Project funded by National Research.
Authors' Contributions
BK, SY, and IJ contributed to the study concept and design; all authors contributed to the methodology, drafted the manuscript, and participated in the manuscript revision; they all read and approved the final manuscript. Subsequently, the final manuscript underwent a comprehensive review and received unanimous approval from all authors.
Conflicts of Interest
None declared.
Search strategy.
DOCX File , 30 KBData extraction instrument.
DOCX File , 16 KBReferences
- Numbers of people with dementia worldwide. Alzheimer's Disease International. URL: https://www.alzint.org/resource/numbers-of-people-with-dementia-worldwide [accessed 2022-07-26]
- Prince M, Wimo A, Guerchet M, Ali G, Wu Y, Prina M. World Alzheimer Report 2015. Alzheimer's Disease International. URL: https://www.alzint.org/u/WorldAlzheimerReport2015.pdf [accessed 2024-07-25]
- Alzheimer's Association. 2023 Alzheimer's disease facts and figures. Alzheimers Dement. Apr 14, 2023;19(4):1598-1695. [CrossRef] [Medline]
- Cantarero-Prieto D, Leon PL, Blazquez-Fernandez C, Juan PS, Cobo CS. The economic cost of dementia: a systematic review. Dementia (London). Nov 2020;19(8):2637-2657. [CrossRef] [Medline]
- Sontheimer N, Konnopka A, König H. The excess costs of dementia: a systematic review and meta-analysis. J Alzheimers Dis. 2021;83(1):333-354. [CrossRef] [Medline]
- Robinson L, Tang E, Taylor J. Dementia: timely diagnosis and early intervention. BMJ. Jun 16, 2015;350:h3029. [FREE Full text] [CrossRef] [Medline]
- Kim B, Noh GO, Kim K. Behavioural and psychological symptoms of dementia in patients with Alzheimer's disease and family caregiver burden: a path analysis. BMC Geriatr. Mar 05, 2021;21(1):160. [FREE Full text] [CrossRef] [Medline]
- Velandia PP, Miller-Petrie MK, Chen C, Chakrabarti S, Chapin A, Hay S, et al. Global and regional spending on dementia care from 2000-2019 and expected future health spending scenarios from 2020-2050: an economic modelling exercise. EClinicalMedicine. Mar 2022;45:101337. [FREE Full text] [CrossRef] [Medline]
- Crous-Bou M, Minguillón C, Gramunt N, Molinuevo JL. Alzheimer's disease prevention: from risk factors to early intervention. Alzheimers Res Ther. Sep 12, 2017;9(1):71. [FREE Full text] [CrossRef] [Medline]
- Aisen PS, Cummings J, Jack CR, Morris JC, Sperling R, Frölich L, et al. On the path to 2025: understanding the Alzheimer's disease continuum. Alzheimers Res Ther. Aug 09, 2017;9(1):60. [FREE Full text] [CrossRef] [Medline]
- Scharre D. Preclinical, prodromal, and dementia stages of Alzheimer's disease. Pract Neurol. 2019:36-47. [FREE Full text]
- Jessen F, Amariglio RE, van BM, Breteler M, Ceccaldi M, Chételat G, et al. A conceptual framework for research on subjective cognitive decline in preclinical Alzheimer's disease. Alzheimers Dement. Nov 2014;10(6):844-852. [FREE Full text] [CrossRef] [Medline]
- Ávila-Villanueva M, Fernández-Blázquez MA. Subjective cognitive decline as a preclinical marker for Alzheimer's disease: the challenge of stability over time. Front Aging Neurosci. 2017;9:377. [FREE Full text] [CrossRef] [Medline]
- Gillis C, Mirzaei F, Potashman M, Ikram MA, Maserejian N. The incidence of mild cognitive impairment: a systematic review and data synthesis. Alzheimers Dement (Amst). Dec 2019;11:248-256. [FREE Full text] [CrossRef] [Medline]
- Jessen F, Amariglio RE, Buckley RF, van der Flier WM, Han Y, Molinuevo JL, et al. The characterisation of subjective cognitive decline. Lancet Neurol. Mar 2020;19(3):271-278. [FREE Full text] [CrossRef] [Medline]
- Mitchell AJ, Shiri-Feshki M. Rate of progression of mild cognitive impairment to dementia--meta-analysis of 41 robust inception cohort studies. Acta Psychiatr Scand. Apr 2009;119(4):252-265. [CrossRef] [Medline]
- Tifratene K, Robert P, Metelkina A, Pradier C, Dartigues JF. Progression of mild cognitive impairment to dementia due to AD in clinical settings. Neurology. Jul 28, 2015;85(4):331-338. [CrossRef] [Medline]
- Pike KE, Cavuoto MG, Li L, Wright BJ, Kinsella GJ. Subjective Cognitive Decline: Level of Risk for Future Dementia and Mild Cognitive Impairment, a Meta-Analysis of Longitudinal Studies. Neuropsychol Rev. Nov 08, 2021:703-735. [CrossRef] [Medline]
- Canevelli M, Grande G, Lacorte E, Quarchioni E, Cesari M, Mariani C, et al. Spontaneous Reversion of Mild Cognitive Impairment to Normal Cognition: A Systematic Review of Literature and Meta-Analysis. J Am Med Dir Assoc. Oct 01, 2016;17(10):943-948. [CrossRef] [Medline]
- Malek-Ahmadi M. Reversion From Mild Cognitive Impairment to Normal Cognition: A Meta-Analysis. Alzheimer Dis Assoc Disord. 2016;30(4):324-330. [CrossRef] [Medline]
- Creese B, Ismail Z. Mild behavioral impairment: measurement and clinical correlates of a novel marker of preclinical Alzheimer's disease. Alzheimers Res Ther. Jan 05, 2022;14(1):2. [FREE Full text] [CrossRef] [Medline]
- Ismail Z, Smith EE, Geda Y, Sultzer D, Brodaty H, Smith G, et al. Neuropsychiatric symptoms as early manifestations of emergent dementia: provisional diagnostic criteria for mild behavioral impairment. Alzheimers Dement. Feb 2016;12(2):195-202. [FREE Full text] [CrossRef] [Medline]
- Ismail Z, McGirr A, Gill S, Hu S, Forkert ND, Smith EE. Mild behavioral impairment and subjective cognitive decline predict cognitive and functional decline. J Alzheimers Dis. 2021;80(1):459-469. [FREE Full text] [CrossRef] [Medline]
- Kapustin D, Zarei S, Wang W, Binns MA, McLaughlin PM, Abrahao A, ONDRI investigators, et al. Neuropsychiatric symptom burden across neurodegenerative disorders and its association with function. Can J Psychiatry. May 2023;68(5):347-358. [FREE Full text] [CrossRef] [Medline]
- Taragano F, Allegri R. Mild behavioral impairment: the early diagnosis. Int Psychogeriatr. 2003;15:12. [FREE Full text]
- Taragano FE, Allegri RF, Krupitzki H, Sarasola DR, Serrano CM, Loñ L, et al. Mild behavioral impairment and risk of dementia: a prospective cohort study of 358 patients. J Clin Psychiatry. Apr 2009;70(4):584-592. [FREE Full text] [CrossRef] [Medline]
- Creese B, Brooker H, Ismail Z, Wesnes KA, Hampshire A, Khan Z, et al. Mild behavioral impairment as a marker of cognitive decline in cognitively normal older adults. Am J Geriatr Psychiatry. Aug 2019;27(8):823-834. [CrossRef] [Medline]
- Ismail Z, Agüera-Ortiz L, Brodaty H, Cieslak A, Cummings J, Fischer CE, et al. The Mild Behavioral Impairment Checklist (MBI-C): a rating scale for neuropsychiatric symptoms in pre-dementia populations. J Alzheimers Dis. 2017;56(3):929-938. [FREE Full text] [CrossRef] [Medline]
- Creese B, Arathimos R, Brooker H, Aarsland D, Corbett A, Lewis C, et al. Genetic risk for Alzheimer's disease, cognition, and mild behavioral impairment in healthy older adults. Alzheimers Dement (Amst). 2021;13(1):e12164. [FREE Full text] [CrossRef] [Medline]
- Gosselin P, Guan DX, Chen H, Pichora-Fuller MK, Phillips N, Faris P, et al. The relationship between hearing and mild behavioral impairment and the influence of sex: a study of older adults without dementia from the COMPASS-ND study. J Alzheimers Dis Rep. 2022;6(1):57-66. [FREE Full text] [CrossRef] [Medline]
- Mallo SC, Ismail Z, Pereiro AX, Facal D, Lojo-Seoane C, Campos-Magdaleno M, et al. Assessing mild behavioral impairment with the Mild Behavioral Impairment-Checklist in people with mild cognitive impairment. J Alzheimers Dis. 2018;66(1):83-95. [CrossRef] [Medline]
- Yokoi Y, Takano H, Sakata M, Maruo K, Nakagome K, Matsuda H. Discrete effect of each mild behavioural impairment category on dementia conversion or cognitive decline in patients with mild cognitive impairment. Psychogeriatrics. Nov 2019;19(6):591-600. [CrossRef] [Medline]
- Taragano FE, Allegri RF, Heisecke SL, Martelli MI, Feldman ML, Sánchez V, et al. Risk of conversion to dementia in a mild behavioral impairment group compared to a psychiatric group and to a mild cognitive impairment group. J Alzheimers Dis. 2018;62(1):227-238. [CrossRef] [Medline]
- Johansson M, Stomrud E, Insel PS, Leuzy A, Johansson PM, Smith R, et al. Mild behavioral impairment and its relation to tau pathology in preclinical Alzheimer's disease. Transl Psychiatry. Jan 26, 2021;11(1):76. [FREE Full text] [CrossRef] [Medline]
- Wolfova K, Creese B, Aarsland D, Ismail Z, Corbett A, Ballard C, et al. Gender/sex differences in the association of mild behavioral impairment with cognitive aging. J Alzheimers Dis. 2022;88(1):345-355. [CrossRef] [Medline]
- Naude JP, Gill S, Hu S, McGirr A, Forkert ND, Monchi O, et al. Alzheimer’s Disease Neuroimaging Initiative. Plasma neurofilament light: a marker of neurodegeneration in mild behavioral impairment. J Alzheimers Dis. 2020;76(3):1017-1027. [FREE Full text] [CrossRef] [Medline]
- Soo SA, Ng KP, Wong F, Saffari SE, Yatawara C, Ismail Z, et al. The association between diabetes mellitus and mild behavioral impairment among mild cognitive impairment: findings from Singapore. J Alzheimers Dis. 2021;82(1):411-420. [CrossRef] [Medline]
- Orso B, Mattei C, Arnaldi D, Massa F, Serafini G, Plantone D, et al. Clinical and MRI predictors of conversion from mild behavioural impairment to dementia. Am J Geriatr Psychiatry. Jul 2020;28(7):755-763. [CrossRef] [Medline]
- Pan Y, Shea Y, Li S, Chen R, Mak HK, Chiu PK, et al. Prevalence of mild behavioural impairment: a systematic review and meta-analysis. Psychogeriatrics. Jan 2021;21(1):100-111. [CrossRef] [Medline]
- Peters MDJ, Marnie C, Tricco AC, Pollock D, Munn Z, Alexander L, et al. Updated methodological guidance for the conduct of scoping reviews. JBI Evid Synth. Oct 2020;18(10):2119-2126. [CrossRef] [Medline]
- Tricco AC, Lillie E, Zarin W, O'Brien KK, Colquhoun H, Levac D, Tunçalp, et al. PRISMA Extension for Scoping Reviews (PRISMA-ScR): checklist and explanation. Ann Intern Med. Oct 02, 2018;169(7):467-473. [CrossRef] [Medline]
- Dobrescu A, Nussbaumer-Streit B, Klerings I, Wagner G, Persad E, Sommer I, et al. Restricting evidence syntheses of interventions to English-language publications is a viable methodological shortcut for most medical topics: a systematic review. J Clin Epidemiol. Sep 2021;137:209-217. [FREE Full text] [CrossRef] [Medline]
- Morrison A, Polisena J, Husereau D, Moulton K, Clark M, Fiander M, et al. The effect of English-language restriction on systematic review-based meta-analyses: a systematic review of empirical studies. Int J Technol Assess Health Care. Apr 2012;28(2):138-144. [CrossRef] [Medline]
- Ageing and health. World Health Organization. URL: https://www.who.int/news-room/fact-sheets/detail/ageing-and-health [accessed 2022-08-08]
Abbreviations
MBI: mild behavioral impairment |
MCI: mild cognitive impairment |
NPI-Q: Neuropsychiatric Inventory Questionnaire |
PRISMA-ScR: Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews |
SCD: subjective cognitive decline |
Edited by T Leung, S Ma; submitted 03.05.24; peer-reviewed by T Phenwan; comments to author 03.06.24; revised version received 18.06.24; accepted 16.07.24; published 29.07.24.
Copyright©Seolah Yoon, Innhee Jeong, Jennifer Ivy Kim, Dahye Hong, Bada Kang. Originally published in JMIR Research Protocols (https://www.researchprotocols.org), 29.07.2024.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Research Protocols, is properly cited. The complete bibliographic information, a link to the original publication on https://www.researchprotocols.org, as well as this copyright and license information must be included.