User:Lichomsm/Early onset dementia
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Early onset dementia (EOD) or young onset dementia (YOD) refers to dementia with symptom onset prior to age 65. This condition is a significant public health concern as the number of individuals with early onset dementia is increasing worldwide[1].
Overview
[edit]Early onset dementia is a general term that describes a group of conditions featuring progressive cognitive decline, particularly in the domains of executive function, learning, language, memory, or behavior. This condition may occur due to various different causes, including degenerative, autoimmune, or infectious processes. The most common form of early onset dementia is Alzheimer's disease, followed by frontotemporal dementia (FTD), and vascular dementia, with Alzheimer's disease accounting for between 40 and 50% of cases[2][3]. Less common forms of early onset dementia include Lewy body dementias (dementia with Lewy bodies and Parkinson's disease dementia), Huntington's disease, Creutzfeldt–Jakob disease, multiple sclerosis, alcohol-induced dementia, and other conditions.
Terminology
[edit]The term young onset dementia is becoming more widely used to avoid the potential confusion between early onset dementia and early stage dementia[4]. Although used in the past, the term presenile dementia is no longer in favor.
Epidemiology
[edit]Early onset dementia is less common than late onset dementia, the former accounting for approximately 10% of dementias globally[3]. Recent studies estimate the prevalence of early onset dementia to be approximately 3.9 million people aged 30-64 worldwide, with an incidence of 119 per 100,000 individuals[1]. Additionally, there is approximately a 1:1 ratio in prevalence of EOD between males and females, with no significant difference between ethnic groups in gender distribution pattern[5][6]. Similar to LOD, the prevalence of EOD increases exponentially with age, doubling every five years of age[5]. The continuous increase in prevalence with age seen in Alzheimer's and FTD versions of EOD is disproportionally led by the most common variant of each cause, namely amnesic Alzheimer's and behavioral variant of FTD[7].
Risk factors
[edit]Traditional risk factors for the development of late onset dementia, such as diabetes mellitus, hypertension, and obesity, have also been identified as risk factors for early onset dementia. Several other chronic conditions have recently been identified that are also associated with the development of early onset dementia, including cardiovascular, respiratory, or gastrointestinal disease[8]. Significantly, the presence of one or multiple of these chronic conditions is more predictive of EOD compared to LOD[8]. Furthermore, the association between low socioeconomic status and the development of dementia is also more pronounced in EOD compared to LOD[9]. Additionally, depending on the specific etiology of EOD, family history may be a significant risk factor, especially for Alzheimer's early onset dementia[6].
Diagnosis
[edit]Though widely accepted, the definition of early onset dementia as less than 65 years of age continues to be an artificial cut-off based on the traditional retirement age in most countries[10]. Nevertheless, the purpose of having a specific age cut-off is evidenced in the significant differences in the etiology and prognosis of dementia depending on the age category of the patient. Furthermore, the diagnosis of early onset dementia continues to be challenging due to the wide range of symptoms at presentation and increased likelihood of not considering neurodegenerative causes in this population. Recent studies indicate an average of 4.4 years time to diagnosis for EOD, compared to 2.8 years for LOD[5]. Indications for the work-up of early onset dementia in this patient population include progressive, unexplained neurological symptoms; new-onset behavioral changes inconsistent with previous personality, especially in patients without significant psychiatric history; or cognitive changes in patients with significant family history of early onset dementia[11]. The diagnostic work-up of early onset dementia includes combinations of detailed history taking, neuroimaging, behavioral testing, and genetic testing[11]. Special considerations for interdisciplinary support should be pursued for younger patients, such as behavioral counseling, social services, or home modifications.
Disease course
[edit]Presentation
[edit]Compared to late onset dementia, patients with early onset dementia are more likely to have dementias other than Alzheimer's disease, although Alzheimer's is the most common etiology in either case[10]. In general, EOD has a faster progression and features more extensive neurological damage when compared to LOD. It is hypothesized that this may be due to decreased cognitive reserve seen in late onset dementias, causing more significant complications relative to pathological damage[10]. Furthermore, studies have shown differences in the areas of cognition that are likely to be affected when comparing early onset to late onset dementia. In terms of behavioral symptoms, EOD is more likely to affect attention, but less likely to cause confusion, delusions, hallucinations, agitation, or disinhibition. In terms of motor symptoms, EOD is less likely to affect verbal fluency and motor executive function compared to late onset dementia[10].
Prognosis
[edit]Estimation of survival rate in early onset dementias is a component patient prognosis, management, and treatment. In general, a better prognosis is positively correlated with earlier age of onset[10]. Average survival time is approximately 6-10 years following diagnosis for both men and women, with variability depending on specific type of dementia[5][12]. The most common cause of immediate death in EOD is respiratory disease (e.g. pneumonia); other causes include cardiovascular events and cerebrovascular disease[10].
References
[edit]- ^ a b Hendriks, Stevie; Peetoom, Kirsten; Bakker, Christian; van der Flier, Wiesje M.; Papma, Janne M.; Koopmans, Raymond; Verhey, Frans R. J.; de Vugt, Marjolein; Köhler, Sebastian; Withall, Adrienne; Parlevliet, Juliette L.; Uysal-Bozkir, Özgül; Gibson, Roger C.; Neita, Susanne M.; Nielsen, Thomas Rune (2021-09). "Global Prevalence of Young-Onset Dementia". JAMA Neurology. 78 (9): 1–11. doi:10.1001/jamaneurol.2021.2161. ISSN 2168-6149. PMC 8290331. PMID 34279544.
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(help) - ^ Quach, C.; Hommet, C.; Mondon, K.; Lauvin, M. A.; Cazals, X.; Cottier, J. P. (2014-04-01). "Early-onset dementias: Specific etiologies and contribution of MRI". Diagnostic and Interventional Imaging. 95 (4): 377–398. doi:10.1016/j.diii.2013.07.009. ISSN 2211-5684.
- ^ a b Krüger, Johanna; Aaltonen, Mikko; Aho, Kalle; Heikkinen, Sami; Kivisild, Ave; Lehtonen, Adolfina; Leppänen, Laura; Rinnankoski, Iina; Soppela, Helmi; Tervonen, Laura; Suhonen, Noora-Maria; Haapasalo, Annakaisa; Portaankorva, Anne M.; Mäki-Petäjä-Leinonen, Anna; Hartikainen, Päivi (2024-08-27). "Incidence and Prevalence of Early-Onset Dementia in Finland". Neurology. 103 (4): e209654. doi:10.1212/WNL.0000000000209654. ISSN 0028-3878. PMID 39047214.
- ^ van de Veen, Dennis; Bakker, Christian; Peetoom, Kirsten; Pijnenburg, Yolande; Papma, Janne; de Vugt, Marjolein; Koopmans, Raymond (2022-03). "Provisional consensus on the nomenclature and operational definition of dementia at a young age, a Delphi study". International Journal of Geriatric Psychiatry. 37 (3): 10.1002/gps.5691. doi:10.1002/gps.5691. ISSN 0885-6230. PMC 9305901. PMID 35156239.
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(help) - ^ a b c d Hendriks, Stevie; Peetoom, Kirsten; Bakker, Christian; Koopmans, Raymond; van der Flier, Wiesje; Papma, Janne; Verhey, Frans; Young‐Onset Dementia Epidemiology Study Group; de Vugt, Marjolein; Köhler, Sebastian (2023-03). "Global incidence of young‐onset dementia: A systematic review and meta‐analysis". Alzheimer's & Dementia. 19 (3): 831–843. doi:10.1002/alz.12695. ISSN 1552-5260.
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(help) - ^ a b Kelly, BJ; Boeve, BF; Josephs, KA (2008). "Young-Onset Dementia: Demographic and Etiologic Characteristics of 235 Patients". jamanetwork.com. Retrieved 2024-10-10.
- ^ Zamboni, Giovanna; Maramotti, Riccardo; Salemme, Simone; Tondelli, Manuela; Adani, Giorgia; Vinceti, Giulia; Carbone, Chiara; Filippini, Tommaso; Vinceti, Marco; Pagnoni, Giuseppe; Chiari, Annalisa (2024). "Age-specific prevalence of the different clinical presentations of AD and FTD in young-onset dementia". Journal of Neurology. 271 (7): 4326–4335. doi:10.1007/s00415-024-12364-7. ISSN 0340-5354. PMID 38643445.
- ^ a b Shang, Xianwen; Zhu, Zhuoting; Zhang, Xueli; Huang, Yu; Zhang, Xiayin; Liu, Jiahao; Wang, Wei; Tang, Shulin; Yu, Honghua; Ge, Zongyuan; Yang, Xiaohong; He, Mingguang (2022-03). "Association of a wide range of chronic diseases and apolipoprotein E4 genotype with subsequent risk of dementia in community-dwelling adults: A retrospective cohort study". EClinicalMedicine. 45: 101335. doi:10.1016/j.eclinm.2022.101335. ISSN 2589-5370. PMC 8921546. PMID 35299656.
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(help) - ^ Li, Rui; Li, Ruyi; Xie, Jinchi; Chen, Junxiang; Liu, Sen; Pan, PhD, An; Liu, PhD, Gang (December 2023). "Associations of socioeconomic status and healthy lifestyle with incident early-onset and late-onset dementia: a prospective cohort study". Healthy Longevity. 4 (12): E693–E702 – via The Lancet.
- ^ a b c d e f Vieira, Renata Teles; Caixeta, Leonardo; Machado, Sergio; Silva, Adriana Cardoso; Nardi, Antonio Egidio; Arias-Carrión, Oscar; Carta, Mauro Giovanni (2013-06-14). "Epidemiology of early-onset dementia: a review of the literature". Clinical Practice and Epidemiology in Mental Health : CP & EMH. 9: 88–95. doi:10.2174/1745017901309010088. ISSN 1745-0179. PMC 3715758. PMID 23878613.
- ^ a b Loi, Samantha M; Cations, Monica; Velakoulis, Dennis (2023-03-06). "Young‐onset dementia diagnosis, management and care: a narrative review". Medical Journal of Australia. 218 (4): 182–189. doi:10.5694/mja2.51849. ISSN 0025-729X. PMC 10952480. PMID 36807325.
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: CS1 maint: PMC format (link) - ^ Kay, David W. K.; Forster, Donald P.; Newens, Andrew J. (2000-08). "Long-term survival, place of death, and death certification in clinically diagnosed pre-senile dementia in northern England: Follow-up after 8–12 years". British Journal of Psychiatry. 177 (2): 156–162. doi:10.1192/bjp.177.2.156. ISSN 0007-1250.
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