Differences in Sex Distribution Between Genetic and Sporadic Frontotemporal Dementia

被引:11
|
作者
de Boer, Sterre C. M. [1 ]
Riedl, Lina [2 ]
van der Lee, Sven J. [1 ]
Otto, Markus [3 ]
Anderl-Straub, Sarah [4 ]
Landin-Romero, Ramon [5 ,6 ]
Sorrentino, Federica [7 ]
Fieldhouse, Jay L. P. [1 ]
Reus, Lianne M. [1 ]
Vacaflor, Blanca [8 ]
Halliday, Glenda [6 ,9 ]
Galimberti, Daniela [7 ,10 ]
Diehl-Schmid, Janine [2 ]
Ducharme, Simon [11 ,12 ]
Piguet, Olivier [5 ,6 ]
Pijnenburg, Yolande A. L. [1 ]
机构
[1] Vrije Univ Amsterdam, Alzheimer Ctr Amsterdam, Dept Neurol, Amsterdam UMC,Amsterdam Neurosci, De Boelelaan 1118, NL-1081 HZ Amsterdam, Netherlands
[2] Tech Univ Munich, Sch Med, Dept Psychiat & Psychotherapy, Munich, Germany
[3] Martin Luther Univ Halle Wittenberg, Univ Clin, Dept Neurol, Halle, Saale, Germany
[4] Univ Clin, Dept Neurol, Ulm, Germany
[5] Univ Sydney, Sch Psychol, Sydney, NSW, Australia
[6] Univ Sydney, Brain & Mind Ctr, Sydney, NSW, Australia
[7] Osped Maggiore Policlin, Neurodegenerat Dis Unit, Fdn IRCCS CaGranda, Milan, Italy
[8] McGill Univ, Dept Psychiat, Hlth Ctr, Montreal, PQ, Canada
[9] Univ Sydney, Sch Med Sci, Sydney, NSW, Australia
[10] Univ Milan, Dino Ferrari Ctr, Dept Biomed Surg & Dent Sci, Milan, Italy
[11] McGill Univ, McConnell Brain Imaging Ctr, Montreal Neurol Inst, Montreal, PQ, Canada
[12] McGill Univ, Douglas Mental Hlth Univ Inst, Dept Psychiat, Montreal, PQ, Canada
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
Behavioral variant frontotemporal dementia; genetic; non-fluent variant primary progressive aphasia; right temporal variant frontotemporal dementia; semantic variant primary progressive aphasia; sex differences; sex distribution; sporadic; PROGRESSIVE SUPRANUCLEAR PALSY; AMYOTROPHIC-LATERAL-SCLEROSIS; BEHAVIORAL VARIANT; LOBAR DEGENERATION; RISK-FACTORS; NEURODEGENERATIVE DISEASE; PREVALENCE; ONSET; AGE; FTD;
D O I
10.3233/JAD-210688
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Reported sex distributions differ between frontotemporal dementia (FTD) cohorts. Possible explanations are the evolving clinical criteria of FTD and its subtypes and the discovery of FTD causal genetic mutations that has resulted in varying demographics. Objective: Our aimwas to determine the sex distribution of sporadic and genetic FTD cases and its subtypes in an international cohort. Methods: We included 910 patients with behavioral variant frontotemporal dementia (bvFTD; n = 654), non-fluent variant primary progressive aphasia (nfvPPA; n = 99), semantic variant primary progressive aphasia (svPPA; n = 117), and right temporal variant frontotemporal dementia (rtvFTD; n = 40). We compared sex distribution between genetic and sporadic FTD using.2-tests. Results: The genetic FTD group consisted of 51.2% males, which did not differ from sporadic FTD (57.8% male, p = 0.08). In the sporadic bvFTD subgroup, males were predominant in contrast to genetic bvFTD (61.6% versus 52.9% males, p = 0.04). In the other clinical FTD subgroups, genetic cases were underrepresented and within the sporadic cases the sex distribution was somewhat equal. Conclusion: The higher male prevalence in sporadic bvFTD may provide important clues for its differential pathogenesis and warrants further research.
引用
收藏
页码:1153 / 1161
页数:9
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