EN

Distribution of neuropsychiatric profiles and comorbid diseases in dementia subtypes

Abstract

Objectives: Alzheimer’s disease (AH) is the most prevalent cause of dementia, followed closely by vascular dementia. Mixed vascular-Alzheimer’s dementia (MVAD) is more evident in individuals aged 80 and above. Frontotemporal dementia (FTD) is the second most common cause of early-onset dementia after AH. Vascular risk factors play important role in the pathogenesis of dementia syndromes. Behavioral and psychological symptoms represent a significant portion of the non-cognitive manifestations in dementia patients. This study aimed to evaluate the distribution of chronic diseases, behavioral disorders, psychiatric findings, and medication use in patients followed with different dementia diagnoses.

Methods: Prevalance of chronic diseases, behavioral disorders, psychiatric findings as well as the usage of antidepressant and antipsychotic medications among patients followed up in dementia outpatient clinics with the diagnosis of AD, mild cognitive impairment (MCI), vascular dementia (VaD), FTD, and MVAD were investigated. Neuropsychiatric inventory (NPI) was applied to the patients.

Results: Four hundred and fifty-five patients were accepted in the study. The patients were distributed as follows: AD (n=303, female/male: 187/115, age = 78±8 years), MCI (n=53, female/male: 31/22, age = 69±10 years), VaD (n=31, female/male: 18/13, age = 68±9 years), FTD (n=32, female/male: 17/15, age = 68±9 years), and MVAD (n=36, female/male: 16/20, age = 76±10 years). Both AD and MVAD groups were significantly older than the other groups (F = 23.2, P<0.0001). The ratio of comorbid chronic diseases was 80% in the AD group, 72% in the MCI group, 91% in the VaD group, 59% in the FTD group, and 93% in the MVAD group. In the whole group, antipsychotic drug use was 27.5% and antidepressant drug use was 28.9%. The mean NPI score was 32.9±28 in antipsychotic users and 16±19 in non-users (P<0.0001). The mean NPI of antidepressant users was 17.6±19 and 21.9±25 (P=0.055) in non-users.

Conclusion: There is a comorbid chronic disease burden in all dementia subtypes, although at varying intensities, and as the chronic disease burden increases, behavioral disorders and psychotic findings increase, and accordingly, the use of antipsychotics also increases.

Keywords

References

  1. 1. Pan WD, Yoshida S, Liu Q, et al. Quantitative evaluation of severity of behavioral and psychological symptoms of dementia in patients with vascular dementia. Transl Neurodegener. 2013;2(1):9. doi: 10.1186/2047-9158-2-9.
  2. 2. Jellinger KA, Attems J. Prevalence of dementia disorders in the oldest-old: an autopsy study. Acta Neuropathol. 2010;119(4):421-433. doi: 10.1007/s00401-010-0654-5.
  3. 3. Knopman DS, Roberts RO. Estimating the number of persons with frontotemporal lobar degeneration in the US population. J Mol Neurosci. 2011;45(3):330-335. doi: 10.1007/s12031-011-9538-y.
  4. 4. Shin IS, Carter M, Masterman D, Fairbanks L, Cummings JL. Neuropsychiatric symptoms and quality of life in Alzheimer disease. Am J Geriatr Psychiatry. 2005;13(6):469-474. doi: 10.1176/appi.ajgp.13.6.469.
  5. 5. Cummings JL. The Neuropsychiatric Inventory: assessing psychopathology in dementia patients. Neurology. 1997;48(5 Suppl 6):S10-16. doi: 10.1212/wnl.48.5_suppl_6.10s.
  6. 6. Cinar N, Sahin S, Karsidag S, et al. Neuropsychiatric Effects of COVID-19 Pandemic on Alzheimer's Disease: A Comparative Study of Total and Partial Lockdown. Sisli Etfal Hastan Tip Bul. 2022;56(4):453-460. doi: 10.14744/SEMB.2022.40326.
  7. 7. McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM. Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology. 1984;34(7):939-944. doi: 10.1212/wnl.34.7.939.
  8. 8. Petersen RC, Stevens JC, Ganguli M, Tangalos EG, Cummings JL, DeKosky ST. Practice parameter: early detection of dementia: mild cognitive impairment (an evidence-based review). Report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. 2001;56(9):1133-1142. doi: 10.1212/wnl.56.9.1133.

Details

APA
Bülbül, N. G., Karşıdağ, S., Çınar, N., Ateş, M. F., Şahin, Ş., Karalı, F. S., Gönül Öner, Ö., Okluoğlu, T., Eren, F., Yılmaz Okuyan, D., Totuk, Ö., Karacan Gölen, M., Acıman Demirel, E., Yıldırım, Z., Erhan, H., Arıca Polat, B. S., Ergin, N., Kobak Tur, E., & Akdoğan, Ö. (2024). Distribution of neuropsychiatric profiles and comorbid diseases in dementia subtypes. The European Research Journal, 10(4), 405-413. https://doi.org/10.18621/eurj.1386582
AMA
1.Bülbül NG, Karşıdağ S, Çınar N, et al. Distribution of neuropsychiatric profiles and comorbid diseases in dementia subtypes. Eur Res J. 2024;10(4):405-413. doi:10.18621/eurj.1386582
Chicago
Bülbül, Nazlı Gamze, Sibel Karşıdağ, Nilgün Çınar, et al. 2024. “Distribution of Neuropsychiatric Profiles and Comorbid Diseases in Dementia Subtypes”. The European Research Journal 10 (4): 405-13. https://doi.org/10.18621/eurj.1386582.
EndNote
Bülbül NG, Karşıdağ S, Çınar N, Ateş MF, Şahin Ş, Karalı FS, Gönül Öner Ö, Okluoğlu T, Eren F, Yılmaz Okuyan D, Totuk Ö, Karacan Gölen M, Acıman Demirel E, Yıldırım Z, Erhan H, Arıca Polat BS, Ergin N, Kobak Tur E, Akdoğan Ö (July 1, 2024) Distribution of neuropsychiatric profiles and comorbid diseases in dementia subtypes. The European Research Journal 10 4 405–413.
IEEE
[1]N. G. Bülbül et al., “Distribution of neuropsychiatric profiles and comorbid diseases in dementia subtypes”, Eur Res J, vol. 10, no. 4, pp. 405–413, July 2024, doi: 10.18621/eurj.1386582.
ISNAD
Bülbül, Nazlı Gamze - Karşıdağ, Sibel - Çınar, Nilgün - Ateş, Miruna Florentina - Şahin, Şevki - Karalı, Fenise Selin - Gönül Öner, Özge et al. “Distribution of Neuropsychiatric Profiles and Comorbid Diseases in Dementia Subtypes”. The European Research Journal 10/4 (July 1, 2024): 405-413. https://doi.org/10.18621/eurj.1386582.
JAMA
1.Bülbül NG, Karşıdağ S, Çınar N, Ateş MF, Şahin Ş, Karalı FS, Gönül Öner Ö, Okluoğlu T, Eren F, Yılmaz Okuyan D, Totuk Ö, Karacan Gölen M, Acıman Demirel E, Yıldırım Z, Erhan H, Arıca Polat BS, Ergin N, Kobak Tur E, Akdoğan Ö. Distribution of neuropsychiatric profiles and comorbid diseases in dementia subtypes. Eur Res J. 2024;10:405–413.
MLA
Bülbül, Nazlı Gamze, et al. “Distribution of Neuropsychiatric Profiles and Comorbid Diseases in Dementia Subtypes”. The European Research Journal, vol. 10, no. 4, July 2024, pp. 405-13, doi:10.18621/eurj.1386582.
Vancouver
1.Nazlı Gamze Bülbül, Sibel Karşıdağ, Nilgün Çınar, Miruna Florentina Ateş, Şevki Şahin, Fenise Selin Karalı, Özge Gönül Öner, Tuğba Okluoğlu, Fettah Eren, Dilek Yılmaz Okuyan, Özlem Totuk, Meltem Karacan Gölen, Esra Acıman Demirel, Zerrin Yıldırım, Hamdi Erhan, Büşra Sümeyye Arıca Polat, Nesrin Ergin, Esma Kobak Tur, Özlem Akdoğan. Distribution of neuropsychiatric profiles and comorbid diseases in dementia subtypes. Eur Res J. 2024 Jul. 1;10(4):405-13. doi:10.18621/eurj.1386582