Mental Health Outcomes in Alzheimer's Disease Patients and Their Partners
Mental Health Outcomes in Alzheimer's Disease Patients and Their Partners
批准号:
10726776
负责人:
Casey Crump
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
已结题
起止时间:
2023-09-01 至 2023-09-02
关键词:
AddressAgeAlzheimer&aposs DiseaseAlzheimer&aposs disease patientAlzheimer&aposs disease related dementiaAnxiety DisordersBirthCessation of lifeChronicCommunitiesDataData SetDementiaDiagnosisDistressEarly InterventionHealthHospital RecordsIncidenceIndividualInpatientsInstitutionInterventionKnowledgeMajor Depressive DisorderMental HealthMental disordersMorbidity - disease rateOutcomeOutpatientsPatient Self-ReportPatientsPersonsPopulationPrevalencePrimary CarePublic HealthQuality of lifeRegistriesRelative RisksReportingResearchResearch PersonnelRiskRisk AssessmentSample SizeSocioeconomic FactorsSpousesStressSubgroupSuicideSuicide attemptSwedenSymptomsTestingTimeUnited States National Institutes of HealthVulnerable Populationsalcohol use disorderburden of illnesscaregivingclinical carecohortcomorbiditycostcost efficientfollow-upglobal healthhigh riskimprovedindexinginnovationmedical specialtiesmortalitynext generationpopulation basedprematurepreventpsychosocialresidencesexsociodemographic factors
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Alzheimer's disease (AD) is a leading cause of morbidity and mortality and is expected to triple in prevalence
worldwide by 2050. AD has a high disease burden that may cause psychosocial distress in AD patients and
their spouses/partners, and may increase risks of mental illness. Importantly, mental disorders are treatable,
and early intervention could reduce suffering, improve quality of life, and prevent premature death in AD
patients and their partners. Despite the high public health burden of mental disorders, they are understudied
compared with somatic outcomes of AD. A comprehensive understanding of mental health sequelae is
critically needed to improve clinical care and outcomes for AD patients and their partners. Prior studies have
had key limitations, including limited follow-up times and sample sizes, and ascertainment of mental disorders
using either self-report which is potentially subject to reporting bias, or hospital records which capture only the
most severe cases. No large-scale studies have included partners. We will address these limitations by
conducting the first comprehensive study of mental health outcomes in AD patients and their partners in a
national cohort (N = 6 M) using highly complete data from primary care, specialty outpatient, and inpatient
settings. We hypothesize that AD patients and their partners have increased risks of major mental disorders
and suicide. To test this hypothesis, we will examine these outcomes in 233,792 persons diagnosed with AD
and 660,807 persons with any dementia (included for comparison with AD findings) in Sweden during 1998-
2018 and their 342,298 partners, compared with 3.3 M without dementia (matched 5:1 on sex and birth year)
and their 1.7 M partners, followed up through 2020. Sweden is an ideal setting because individual-level data
on AD and all-cause dementia diagnoses, mental health outcomes, and covariates are available for the entire
population. Moreover, the incidence and treatment of AD and common mental disorders are comparable to the
US. Our specific aims are to determine risks of 4 major mental health outcomes (major depression, anxiety
disorders, alcohol use disorder, and suicide) in AD and all-cause dementia patients and their spouses/partners,
and identify high-risk subgroups. The proposed research is significant because AD is a major global health
problem that is increasing in prevalence, and its mental health sequelae may have substantial impacts that are
understudied and preventable or treatable. It is innovative because it will provide the first comprehensive
assessment of 4 major mental health outcomes in a national cohort of AD and all-cause dementia patients and
their partners by integrating unparalleled individual-level data for 6 M people. It is highly cost-efficient because
we will leverage data from multiple national registries in Sweden that are unavailable or prohibitively costly to
assemble in the US. The results will fill critical knowledge gaps by identifying, for the first time, mental health
outcomes in AD and all-cause dementia patients, their partners, and high-risk subgroups in a national
population, which will help guide timely interventions to improve their quality of life and health outcomes.
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