Abstract
It is predictable that syndromes of frontotemporal dementia (FTD) may have a worldwide distribution; however, data available on their incidence and prevalence are variable. This variability most likely reflects disparities across regions in the distribution of the expertise, technology, and resources available for FTD research and care. Important discoveries have been made regarding FTD’s phenotypes, genetics, and cultural influences on the expression of symptoms; however, in many countries, there are barriers posed by a dearth of resources. There are pressing needs to further develop research on FTD: including first, population studies designed to fill the gaps in our knowledge about FTD’s frequency and risk factors in developing regions and among minority groups in developed countries. It is also necessary to facilitate the psychometric characterization of contemporary diagnostic criteria and their translation to different languages and cultural contexts. Furthermore, much needed is the analysis of differences in the genetic risk factors for FTD, particularly non-Mendelian susceptibility factors. It is hoped that reflections on FTD from an international perspective will spur an extension of the vibrant multicenter collaborations, that exist in North America and Europe, toward new centers to be established and supported in the developing regions of the world.
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References
Velakoulis D, Walterfang M, Mocellin R et al (2009) Frontotemporal dementia presenting as schizophrenia-like psychosis in young people: clinicopathological series and review of cases. Br J Psychiatry 194:298–305
Baborie A, Baborie A, Griffiths TD et al (2012) Frontotemporal dementia in elderly individuals. Arch Neurol 69:1052–1060
Kertesz A, McMonagle P, Blair M et al (2005) The evolution and pathology of frontotemporal dementia. Brain 128:1996–2005
Withall A, Draper B, Seeher K et al (2014) The prevalence and causes of younger onset dementia in eastern Sydney, Australia. Int Psychogeriatr 26:1955–1965
Herrera E, Caramelli P, Silveira ASB et al (2002) Epidemiologic survey of dementia in a community-dwelling Brazilian population. Alzheimer Dis Assoc Disord 16:103–108
Nitrini R, Caramelli P, Herrera E et al (2004) Incidence of dementia in a community-dwelling Brazilian population. Alzheimer Dis Assoc Disord 18:241–246
Feldman HH, Feldman H, Levy AR et al (2003) A Canadian cohort study of cognitive impairment and related dementias (ACCORD): study methods and baseline results. Neuroepidemiology 22:265–274
Kivipelto M, Helkala E-L, Laakso MP et al (2002) Apolipoprotein E epsilon4 allele, elevated midlife total cholesterol level, and high midlife systolic blood pressure are independent risk factors for late-life Alzheimer disease. Ann Intern Med 137:149–155
Ibach B, Koch H, Koller M et al (2003) Hospital admission circumstances and prevalence of frontotemporal lobar degeneration: a multicenter psychiatric state hospital study in Germany. Dement Geriatr Cogn Disord 16:253–264
Banerjee TK, Mukherjee CS, Dutt A et al (2008) Cognitive dysfunction in an urban Indian population – some observations. Neuroepidemiology 31:109–114
Ravaglia G, Forti P, Maioli F et al (2005) Incidence and etiology of dementia in a large elderly Italian population. Neurology 64:1525–1530
Gilberti N, Turla M, Alberici A et al (2012) Prevalence of frontotemporal lobar degeneration in an isolated population: the Vallecamonica study. Neurol Sci 33:899–904
Borroni B, Alberici A, Grassi M et al (2010) Is frontotemporal lobar degeneration a rare disorder? Evidence from a preliminary study in Brescia county, Italy. J Alzheimers Dis 19:111–116
Borroni B, Alberici A, Grassi M et al (2011) Prevalence and demographic features of early-onset neurodegenerative dementia in Brescia County, Italy. Alzheimer Dis Assoc Disord 25:341–344
Bernardi L, Frangipane F, Smirne N et al (2012) Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy. Neurobiol Aging 33:2948.e1–2948.e10
Ikeda M, Hokoishi K, Maki N et al (2001) Increased prevalence of vascular dementia in Japan: a community-based epidemiological study. Neurology 57:839–844
Yamada T, Hattori H, Miura A et al (2001) Prevalence of Alzheimer’s disease, vascular dementia and dementia with Lewy bodies in a Japanese population. Psychiatry Clin Neurosci 55:21–25
Wada-Isoe K, Uemura Y, Suto Y et al (2009) Prevalence of dementia in the rural island town of Ama-cho, Japan. Neuroepidemiology 32:101–106
Ikejima C, Yasuno F, Mizukami K et al (2009) Prevalence and causes of early-onset dementia in Japan: a population-based study. Stroke 40:2709–2714
Wada-Isoe K, Ito S, Adachi T et al (2012) Epidemiological survey of frontotemporal lobar degeneration in Tottori prefecture, Japan. Dement Geriatr Cogn Dis Extra 2:381–386
Rosso SM, Donker Kaat L, Baks T et al (2003) Frontotemporal dementia in the Netherlands: patient characteristics and prevalence estimates from a population-based study. Brain 126:2016–2022
Amoo G, Akinyemi RO, Onofa LU et al (2011) Profile of clinically-diagnosed dementias in a neuropsychiatric practice in Abeokuta, South-Western Nigeria. Afr J Psychiatry (Johannesbg) 14:377–382
Gascón-Bayarri J, Reñé R, Del Barrio JL et al (2007) Prevalence of dementia subtypes in El prat de Llobregat, Catalonia, Spain: the PRATICON study. Neuroepidemiology 28:224–234
Garre-Olmo J, Genís Batlle D, del Mar Fernández M et al (2010) Incidence and subtypes of early-onset dementia in a geographically defined general population. Neurology 75:1249–1255
Lee DY, Lee JH, Ju Y-S et al (2002) The prevalence of dementia in older people in an urban population of Korea: the Seoul study. J Am Geriatr Soc 50:1233–1239
Andreasen N, Blennow K, Sjödin C et al (1999) Prevalence and incidence of clinically diagnosed memory impairments in a geographically defined general population in Sweden. The Piteå Dementia Project Neuroepidemiology 18:144–155
Gislason TB, Sjögren M, Larsson L et al (2003) The prevalence of frontal variant frontotemporal dementia and the frontal lobe syndrome in a population-based sample of 85 year olds. J Neurol Neurosurg Psychiatry 74:867–871
Gurvit H, Emre M, Tinaz S et al (2008) The prevalence of dementia in an urban Turkish population. Am J Alzheimers Dis Other Dement 23:67–76
Ratnavalli E, Ratnavalli E, Brayne C et al (2002) The prevalence of frontotemporal dementia. Neurology 58:1615–1621
Stevens T, Livingston G, Kitchen G et al (2002) Islington study of dementia subtypes in the community. Br J Psychiatry 180:270–276
Harvey RJ, Skelton-Robinson M, Rossor MN (2003) The prevalence and causes of dementia in people under the age of 65 years. J Neurol Neurosurg Psychiatry 74:1206–1209
Mercy L, Hodges JR, Dawson K et al (2008) Incidence of early-onset dementias in Cambridgeshire, United Kingdom. Neurology 71:1496–1499
Coyle-Gilchrist ITS, Dick KM, Patterson K et al (2016) Prevalence, characteristics, and survival of frontotemporal lobar degeneration syndromes. Neurology 86:1736–1743
Knopman DS, Petersen RC, Edland SD et al (2004) The incidence of frontotemporal lobar degeneration in Rochester, Minnesota, 1990 through 1994. Neurology 62:506–508
Hogan DB, Jetté N, Fiest KM et al (2016) The prevalence and incidence of frontotemporal dementia: a systematic review. Can J Neurol Sci 43(Suppl 1):S96–S109
Phung TKT, Waltoft BL, Kessing LV et al (2010) Time trend in diagnosing dementia in secondary care. Dement Geriatr Cogn Disord 29:146–153
Onyike CU, Diehl-Schmid J (2013) The epidemiology of frontotemporal dementia. Int Rev Psychiatry 25:130–137
Knopman DS, Roberts RO (2011) Estimating the number of persons with frontotemporal lobar degeneration in the US population. J Mol Neurosci 45:330–335
Lekoubou A, Echouffo-Tcheugui JB, Kengne AP (2014) Epidemiology of neurodegenerative diseases in sub-Saharan Africa: a systematic review. BMC Public Health 14:653
Rascovsky K, Hodges JR, Kipps CM et al (2007) Diagnostic criteria for the behavioral variant of frontotemporal dementia (bvFTD): current limitations and future directions. Alzheimer Dis Assoc Disord 21:S14–S18
Rascovsky K, Hodges JR, Knopman D et al (2011) Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia. Brain 134:2456–2477
Gorno-Tempini ML, Hillis AE, Weintraub S et al (2011) Classification of primary progressive aphasia and its variants. Neurology 76:1006–1014
Lamarre AK, Rascovsky K, Bostrom A et al (2013) Interrater reliability of the new criteria for behavioral variant frontotemporal dementia. Neurology 80:1973–1977
Harris JM, Gall C, Thompson JC et al (2013) Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia. Neurology 80:1881–1887
Poorkaj P, Bird TD, Wijsman E et al (1998) Tau is a candidate gene for chromosome 17 frontotemporal dementia. Ann Neurol 43:815–825
Hutton M, Lendon CL, Rizzu P et al (1998) Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nat Publ Group 393:702–705
Spillantini MG, Murrell JR, Goedert M et al (1998) Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc Natl Acad Sci 95:7737–7741
Baker M, Mackenzie IR, Pickering-Brown SM et al (2006) Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17. Nature 442:916–919
Cruts M, Gijselinck I, van der Zee J et al (2006) Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21. Nature 442:920–924
DeJesus-Hernandez M, Mackenzie IR, Boeve BF et al (2011) Expanded GGGGCC hexanucleotide repeat in noncoding region of C9orf72 causes chromosome 9p-linked FTD and ALS. Neuron 72:245–256
Renton AE, Majounie E, Waite A et al (2011) A hexanucleotide repeat expansion in C9orf72 is the cause of chromosome 9p21-linked ALS-FTD. Neuron 72:257–268
Greaves CV, Rohrer JD (2019) An update on genetic frontotemporal dementia. J Neurol 266:2075–2086
Benussi L, Ghidoni R, Pegoiani E et al (2009) Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide. Neurobiol Dis 33:379–385
Borroni B, Bonvicini C, Galimberti D et al (2011) Founder effect and estimation of the age of the Progranulin Thr272fs mutation in 14 Italian pedigrees with frontotemporal lobar degeneration. Neurobiol Aging 32:555.e1–555.e8
Majounie E, Renton AE, Mok K et al (2012) Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study. Lancet Neurol 11:323–330
Kartanou C, Karadima G, Koutsis G et al (2018) Screening for the C9orf72 repeat expansion in a greek frontotemporal dementia cohort. Amyotroph Lat Scl Frr 19:152–154
Guven G, Lohmann E, Bras J et al (2016) Mutation frequency of the major Frontotemporal dementia genes, MAPT, GRN and C9orf72 in a Turkish cohort of dementia patients. PLoS One 11:e0162592
Pliner HA, Mann DM, Traynor BJ (2014) Searching for Grendel: origin and global spread of the C9orf72 repeat expansion. Acta Neuropathol 127:391–396
Cintra VP, Bonadia LC, Andrade HMT et al (2018) The frequency of the C9orf72 expansion in a Brazilian population. Neurobiol Aging 66:179.e1–179.e4
Jiao B, Tang B, Liu X et al (2014) Identification of C9orf72 repeat expansions in patients with amyotrophic lateral sclerosis and frontotemporal dementia in mainland China. Neurobiol Aging 35:936.e19–936.e22
Sirkis DW, Geier EG, Bonham LW et al (2019) Recent advances in the genetics of frontotemporal dementia. Curr Genet Med Rep 7:41–52
Fukuhara R, Ghosh A, Fuh J-L et al (2014) Family history of frontotemporal lobar degeneration in Asia – an international multi-center research. Int Psychogeriatr 26:1967–1971
Bannwarth S, Ait-El-Mkadem S, Chaussenot A et al (2014) A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement. Brain 137:2329–2345
Jiao B, Xiao T, Hou L et al (2016) High prevalence of CHCHD10 mutation in patients with frontotemporal dementia from China. Brain 139:e21–e21
Che X-Q, Zhao Q-H, Huang Y et al (2017) Genetic features of MAPT, GRN, C9orf72 and CHCHD10 gene mutations in Chinese patients with Frontotemporal dementia. Curr Alzheimer Res 14:1102–1108
Aswathy PM, Jairani PS, Raghavan SK et al (2016) Progranulin mutation analysis: identification of one novel mutation in exon 12 associated with frontotemporal dementia. Neurobiol Aging 39:218.e1–218.e3
Jiao B, Guo J-F, Wang Y-Q et al (2013) C9orf72 mutation is rare in Alzheimer’s disease, Parkinson’s disease, and essential tremor in China. Front Cell Neurosci 7:164
Lin C-H, Chen T-F, Chiu M-J et al (2014) Lack of c9orf72 repeat expansion in Taiwanese patients with mixed neurodegenerative disorders. Front Neurol 5:59
Tang M, Gu X, Wei J et al (2016) Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia. Neurobiol Aging 46:235.e11–235.e15
Ogaki K, Ogaki K, Li Y et al (2013) Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBS. Parkinsonism Relat Disord 19:15–20
Jang J-H, Kwon M-J, Choi WJ et al (2013) Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis. Neurobiol Aging 34:1311.e7–1311.e9
Kim E-J, Kwon JC, Park KH et al (2014) Clinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementia. Neurobiol Aging 35:1213.e13–1213.e17
Das G, Sadhukhan T, Sadhukhan D et al (2013) Genetic study on frontotemporal lobar degeneration in India. Parkinsonism Relat Disord 19:487–489
Mukherjee O, Das G, Sen S et al (2015) C9orf72 mutations may be rare in frontotemporal lobar degeneration patients in India. Amyotroph Lateral Scler Frontotemporal Degener 17:151–153
Josephs K, Hu W, Hillis A et al (2016) Frontotemporal dementia in patients of African descent. J Neurochem 138:229
Ghosh A, Dutt A, Ghosh M et al (2013) Using the revised diagnostic criteria for Frontotemporal dementia in India: evidence of an advanced and florid disease. PLoS One 8:e60999
Ghosh A, Dutt A (2010) Utilisation behaviour in frontotemporal dementia. J Neurol Neurosurg Psychiatry 81:154–156
Akinyemi RO, Akinyemi RO, Owolabi MO et al (2009) Frontotemporal dementia in a Nigerian woman: case report and brief review of the literature. Afr J Med Med Sci 38:71–75
Shinagawa S, Ikeda M, Nestor PJ et al (2009) Characteristics of abnormal eating behaviours in frontotemporal lobar degeneration: a cross-cultural survey. J Neurol Neurosurg Psychiatry 80:1413–1414
Tanabe H (2007) The uniqueness of Gogi aphasia owing to temporal lobar atrophy. Alzheimer Dis Assoc Disord 21:S12–S13
Ellajosyula R, Narayanan J, Patterson K (2020) Striking loss of second language in bilingual patients with semantic dementia. J Neurol 267:551–560
Alladi S, Bak TH, Shailaja M et al (2017) Bilingualism delays the onset of behavioral but not aphasic forms of frontotemporal dementia. Neuropsychologia 99:207–212
Kansal K, Mareddy M, Sloane KL et al (2016) Survival in Frontotemporal dementia phenotypes: a meta-analysis. Dement Geriatr Cogn Disord 41:109–122
Dias A, Patel V (2009) Closing the treatment gap for dementia in India. Indian J Psychiatry 51(Suppl 1):S93–S97
Kamoga R, Rukundo GZ, Wakida EK et al (2019) Dementia assessment and diagnostic practices of healthcare workers in rural southwestern Uganda: a cross-sectional qualitative study. BMC Health Serv Res 19:1005
Wylie MA, Shnall A, Onyike CU et al (2013) Management of frontotemporal dementia in mental health and multidisciplinary settings. Int Rev Psychiatry 25:230–236
Stoner CR, Lakshminarayanan M, Durgante H et al (2019) Psychosocial interventions for dementia in low- and middle-income countries (LMICs): a systematic review of effectiveness and implementation readiness. Aging Ment Health 6:1–12
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Onyike, C.U., Shinagawa, S., Ellajosyula, R. (2021). Frontotemporal Dementia: A Cross-Cultural Perspective. In: Ghetti, B., Buratti, E., Boeve, B., Rademakers, R. (eds) Frontotemporal Dementias . Advances in Experimental Medicine and Biology, vol 1281. Springer, Cham. https://doi.org/10.1007/978-3-030-51140-1_10
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