Skip to main content

ORIGINAL RESEARCH article

Front. Aging Neurosci., 28 April 2020
Sec. Alzheimer's Disease and Related Dementias
This article is part of the Research Topic Translational Advances in Alzheimer's, Parkinson's, and other Neurodegenerative Dementias View all 70 articles

Freezing of Speech Single Questionnaire as a Screening Tool for Cognitive Dysfunction in Patients With Dementia With Lewy Bodies

\r\nPai-Yi ChiuPai-Yi Chiu1Guang-Uei HungGuang-Uei Hung2Cheng-Yu WeiCheng-Yu Wei3Ray-Chang TzengRay-Chang Tzeng4Ming-Chyi Pai,,*Ming-Chyi Pai5,6,7*
  • 1Department of Neurology, Show Chwan Memorial Hospital, Changhua, Taiwan
  • 2Department of Nuclear Medicine, Chang Bing Show Chwan Memorial Hospital, Changhua, Taiwan
  • 3Department of Neurology, Chang Bing Show Chwan Memorial Hospital, Changhua, Taiwan
  • 4Department of Neurology, Tainan Municipal Hospital, Tainan, Taiwan
  • 5Division of Behavioral Neurology, Department of Neurology, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan
  • 6Alzheimer’s Disease Research Center, National Cheng Kung University Hospital, Tainan, Taiwan
  • 7Institute of Gerontology, College of Medicine, National Cheng Kung University, Tainan, Taiwan

Introduction: Freezing phenomenon is a striking feature of Parkinson’s disease. However, it has never been studied in people with dementia with Lewy bodies (DLB). We designed a freezing of speech single questionnaire (FOSSQ) and investigated the frequency and association of freezing of speech (FOS) in patients with DLB and other types of dementia.

Methods: This is a retrospective analysis of data from the project of history-based artificial intelligent computerized dementia diagnostic system. We compared the frequencies of FOS among non-demented (ND) participants, patients with Alzheimer’s disease (AD), vascular dementia (VaD), and DLB. Further, we explored the association factors of FOS in all the participants.

Results: We enrolled 666 individuals with the following disease distribution: 190, ND; 230, AD; 183, VaD; and 63, DLB. Compared to individuals with ND (2.1%), patients with AD (6.1%), or VaD (18.0%), DLB (54.0%) showed a significantly higher frequency of positive FOS (all p < 0.001). The association factors of FOS were older age, more severe dementia, more severe motor dysfunction, fluctuating cognition, visual hallucinations, parkinsonism, rapid eye movement sleep behavior disorder, attention, mental manipulation, and language.

Conclusion: Our study showed that the informant-based FOSSQ may be a practical screening tool for discriminating DLB from individuals with ND or other forms of dementia. The FOSSQ can be applied in clinical practice as well as on the artificial intelligent platform.

Introduction

Freezing phenomenon is a striking feature of Parkinson’s disease (PD). Freezing of gait (FOG) is a form of akinesia and is one of the most disabling symptoms of PD (Giladi et al., 2001). Previous studies on FOG in PD have reported a prevalence of 7.1–46% (Giladi et al., 2001; Macht et al., 2007) according to different criteria. However, there have only been a few studies on the freezing of speech (FOS) phenomenon (Ackermann et al., 1993; Giladi et al., 1997; Louis et al., 2001; Park et al., 2014; Vercruysse et al., 2014) in PD. Further, freezing phenomenon has rarely been mentioned or studied in neurological disorders other than PD, with some mentioning the phenomenon of FOS sharing a similar neural mechanism with FOG (Park et al., 2014; Vercruysse et al., 2014). The underlying mechanism of the freezing phenomenon is probably related to dysfunction of the fronto-striatal circuits (Vercruysse et al., 2014). To our knowledge, there have been no studies on FOS in dementia with Lewy bodies (DLB) or other degenerative types of dementia. DLB is one of the Lewy body diseases (LBD) and it shares a similar pathological manifestation with PD, especially PD with dementia (PDD) (Kosaka et al., 1984; Jellinger, 2018). Therefore, patients with DLB should demonstrate similar freezing phenomenon as PD/PDD. It remains unclear whether FOS is a deficit of language or other cognitive functions. However, language dysfunction is indeed one of the common cognitive features of a diagnosis of dementia due to Alzheimer’s disease (AD) or other forms of dementia (McKeith et al., 2005; McKhann et al., 2011; Hardy et al., 2016). Similarly, the association factors of FOS have not yet been well studied.

To study FOS, we designed a simple informant-based FOS single questionnaire (FOSSQ) that was embedded in the History-based Artificial Intelligent Clinical Dementia Diagnostic System (HAICDDS) (Lin et al., 2018; Chiu et al., 2019). We aimed to investigate the frequency and association of FOS in DLB and other types of dementia. We proposed that since the FOS phenomenon is a striking feature of PD, it could be an important feature of DLB because both language (Lin et al., 2018) and motor deficits (McKeith et al., 2005) are common clinical presentations of DLB. Based on the findings that the underlying mechanism of the freezing phenomenon is probably related to dysfunction of the fronto-striatal circuits (Vercruysse et al., 2014), we proposed that FOS could be a deficit involving language and motor dysfunction as well as dysfunction of other cognitive functions such as attention and executive dysfunction. Similarly, as a striking clinical phenomenon, we also proposed that FOS may involve fluctuation of attention and cognition, and thus performed fluctuation scale comparisons.

Materials and Methods

This is a sub-study of the project of HAICDDS, which is currently used as a registration platform in the Show Chwan Healthcare System (Lin et al., 2018; Chiu et al., 2019). Participants who visited either hospital of the healthcare system with suspected cognitive or motor dysfunction were registered with their demographical, clinical, cognitive, neuropsychiatric, motor, laboratory, and neuroimaging data in the database. The HAICDDS questionnaire is part of the database for recording of clinical history. It is composed of 100 questions designed after a consensus meeting of 12 neurologists, one geriatric psychiatrist, three nuclear medicine doctors, and one neuroradiologist. The fundamental structure of the questionnaire is similar to that of history-taking used by physicians for acquiring detailed clinical information. Before commencing the project, thirty patients with their informants were assessed by neuropsychologists from three centers and the reproducibility was studied using the interrater reliability analysis. Cronbach’s alpha coefficient was calculated to estimate the reliability of the entire novel screening questionnaire. The original writing of FOSSQ was in Chinese as follows: 跟人講話時常常思緒突然中斷,腦袋好像一片空白,難以互動嗎 (The tentative translation to English is: “When speaking, does he/she pause frequently, seem blank, and have trouble communicating?”). In this sub-study, we analyzed and compared the FOSSQ results among non-demented (ND) participants as well as participants with AD, vascular dementia (VaD), and DLB. Further, we studied the association factors of FOS among the participants.

Diagnosis of AD, VaD, or DLB

A diagnosis of AD was made according to the criteria for dementia due to AD developed by the National Institute on Aging-Alzheimer’s Association workgroups on diagnostic guidelines for AD (McKhann et al., 2011). A diagnosis of VaD was made according to the criteria for probable VaD or possible VaD in the 2011 AHA/ASA criteria for vascular cognitive impairment (VCI) (Gorelick et al., 2011). A diagnosis of DLB was made according to the revised consensus criteria for probable DLB developed by the fourth report of the DLB consortium (McKeith et al., 2017).

Diagnosis of ND, or Different Stages of Dementia

ND participant was diagnosed with a global CDR (Morris, 1993) score of 0 or 0.5 without significantly impaired activities of daily living, which was defined by an Instrumental Activities of Daily Living (IADL) score greater than 6 (Mao et al., 2018). A diagnosis of dementia was made according to the criteria for dementia developed by the NIA-AA (McKhann et al., 2011). Specifically, people with dementia had impairments in two cognitive domains or more as well as declined daily functions (at least one of the domains of community affairs, home hobbies, and personal care with a CDR score ≥ 0.5 and an IADL score ≤ 6) (Mao et al., 2018). Dementia severity was defined by the global CDR scale score; specifically, participants with a global CDR score of 0.5, 1, 2, and 3 were defined as having very mild, mild, moderate, and severe dementia, respectively (Morris, 1993).

Procedure of the Study

This is a retrospective analysis of data from the HAICDDS, which is currently applied in three centers in Taiwan (two in central Taiwan and one in southern Taiwan). Daily function was assessed using the Instrumental Activities of Daily Living (IADL) Scale (Lawton and Brody, 1969). Cognitive function was assessed using the Cognitive Abilities Screening Instrument (CASI) (Lin et al., 2002) and the Montreal Cognitive Assessment (MoCA) (Chen et al., 2016). Neuropsychiatric symptoms were assessed using the Neuropsychiatric Inventory (NPI) (Cummings, 1988). Language function was assessed using the language subscales in the CASI and HAICDDS (HAICDDS-Language) (Lin et al., 2018). Language domain in CASI screens cognitive performance on reading, writing, naming, and comprehension whereas, language questions in HAICDDS acquire information on speech fluency, comprehension, naming, volume, and tone based on clinical history (Lin et al., 2018). Trained neuropsychologists administered the cognitive tests and NPI to all the patients.

Statistics

The Chinese version of SPSS 22.0 for Windows (IBM, SPSS Inc., Chicago) was used for statistical analyses. Between-group comparisons of demographic data, neuropsychological tests, CDR sum of boxes (CDR-SB), IADL score, MoCA score, CASI score, NPI total score (NPI-sum), motor subscale of the Unified Parkinson’s Disease Rating Scale (UPDRS-M), and DLB features were analyzed using independent t-test or one-way ANOVA with either Bonferroni or Dunnett T3 post hoc analysis according to the homogeneity of variance. Between-group comparisons of demographic and background characteristics with positive FOSSQ (FOSSQ +) and negative FOSSQ (FOSSQ-) were adjusted for age and disease severity. Comparisons of each cognitive domain in the CASI between FOSSQ + and FOSSQ- groups were adjusted for age, gender, and disease severity. Comparison of frequency of symptom fluctuation in the Mayo Fluctuation Composite Score (MFCS) and language symptoms in the HAICDDS-Language between FOSSQ + and FOSSQ- groups were adjusted for age and disease severity.

Ethical Consideration

The participants were selected from a registry-based database of the Show Chwan Health System. The study design was retrospective, and the data were anonymously analyzed. The Committee for Medical Research Ethics of Show Chwan Memorial Hospital reviewed the project and the Data Inspectorate approved the study.

Results

We enrolled 666 individuals with the following disease distribution: 190, ND; 230, AD; 183, VaD; and 63, DLB. The frequency of FOSSQ + in patients with CDR scores of 0, 0.5, 1, 2, and 3 were 3.8, 3.0, 15.2, 26.1, and 43.5%, respectively. Compared to patients with ND (2.1%), AD (6.1%), or VaD (18.0%), those with DLB (54.0%) showed a significantly higher frequency of FOSSQ + (all p < 0.001). Comparison of demographic and background characteristics among patients with ND, AD, VaD, and DLB revealed significant differences in all the parameters (p < 0.001), except for informant age or education (Table 1).

TABLE 1
www.frontiersin.org

Table 1. Comparison of demographic data among ND, AD, VaD, and DLB groups.

Comparison of demographic and background characteristics between the FOSSQ + and FOSSQ- groups before adjustment revealed that the FOSSQ + group had a significantly older age and more severe dementia stages. Further, there were significant differences in all other parameters (p < 0.001) except for gender, education, and history of cerebrovascular accident (Table 2). After adjustment for age and disease severity, FOSSQ + had more males and higher DLB features including UPDRS-M, cognitive fluctuations, visual hallucinations, parkinsonism, and REM sleep behavior disorder (Table 2).

TABLE 2
www.frontiersin.org

Table 2. Comparison of demographic and background characteristics between groups with FOSSQ + and FOSSQ – adjusted for age and disease severity according to CDR.

Comparison of each cognitive domain in the CASI between the FOSSQ + and FOSSQ- groups before adjustment revealed that the FOSSQ + group had significantly lower scores in all domains (p < 0.001). After adjustment for age and disease severity, the FOSSQ + group had significantly lower scores only in the attention and language domains (Table 3).

TABLE 3
www.frontiersin.org

Table 3. Comparison of each cognitive domain in CASI between groups with FOSSQ + and FOSSQ – adjusted for age, education, gender, and disease severity according to CDR.

Comparison of frequency of symptom fluctuation in the MFCS and language symptoms in the HAICDDS-Language between FOSSQ + and FOSSQ- before and after adjustment for age and disease severity showed that FOSSQ + had a significantly higher frequency in all domains in the MFCS and HAICDDS-Language except for language impairment, which occurred much earlier than the other symptoms (HAICDDS-L7) (Table 4). Given our recent finding that HAICDDS-L8 has the highest power for discrimination of DLB when compared to other types of dementia (Lin et al., 2018), we further combined FOSSQ with HAICDDS-L8 and found that the positive rate for each question were DLB (61.9%), VaD (29.0%), AD (7.8%), and ND (2.6%).

TABLE 4
www.frontiersin.org

Table 4. Comparison of frequency of fluctuation symptoms in MFCS and language symptoms in HAICDDS-Language between groups with FOSSQ + and FOSSQ – adjusted for age and disease severity according to CDR.

Discussion

As a sub-study of the project HAICDDS, we analyzed data from a relatively large population (666 individuals) and obtained important results. First, we successfully demonstrated that even a single question could provide good discrimination among dementia stages and subtypes. The frequencies of FOSSQ + in patients with CDR scores of 0, 0.5, 1, 2, and 3 were 3.8, 3.0, 15.2, 26.1, and 43.5%, respectively, indicating that the frequency of FOS significantly increased with increase in dementia severity. Regarding discrimination of dementia subtypes, the FOS phenomenon was found more often in patients with DLB (54.0%) compared to those with either AD (6.1%) or VaD (18.0%). The frequency of FOSSQ + was lower among females, which is consistent with previous findings on freezing phenomenon in Parkinson’s disease (Park et al., 2014).

Second, the frequency of FOS was not only highest in patients with DLB but was also more significantly associated with DLB features (p < 0.001), including cognitive fluctuations (OR = 10.22), visual hallucinations (OR = 4.18), parkinsonism (OR = 4.68), and REM sleep behavior disorder (OR = 2.84). Motor dysfunction according to the UPDRS-M is more severe in the FOSSQ + group (OR = 1.02; p = 0.002). Therefore, it is reasonable to consider FOS as part of the characteristic features in the diagnosis of DLB than that of ND or other types of dementia. The dopamine transporter imaging is not significantly different after adjustment, however. We proposed that non-DLB participants who performed dopamine transporter imaging were comorbid with motor dysfunction and were highly suspected to have parkinsonism. Hence, a relatively high percentage of DaTabN was found among these patients (47.1 and 20% in VaD and AD). Our next piece of research to address this issue and to clarify the association of FOS and dopamine transporter uptake in the striatal area is underway.

Third, after adjustment for age and dementia severity, the FOSSQ + demonstrated a strong relationship with dysfunctions in attention, mental manipulation, and language domains in the CASI. This indicated that FOS might be a combination of these types of cognitive dysfunction, which is consistent with our hypothesis. Some researchers may argue that using the cognitive screening tool CASI, attention domain screens only registration and repetition and language domain screening cognitive performance on reading, writing, naming, and comprehension. Whether attention and language subscales in CASI represent the actual functions of attention and language might be controversial based only on a cognitive screening tool. Further detailed and specific neuropsychological tests to clarify the association of FOS with cognitive functions will be necessary.

Fourth, it is consistent with our recent findings of language dysfunction being more severe in patients with DLB than those with other dementia using the HAICDDS-Language questionnaire (Lin et al., 2018). In the study, we found that the discriminative ability of the HAICDDS-Language, especially the HAICDDS-L8 (“Does his/her speech reduce pitch range and reduced volume?”) among patients with DLB/PDD and AD was robust (OR = 9.16; 95% CI: 6.33–13.25) (Lin et al., 2018). Therefore, in the current study, we combined the FOSSQ with HAICDDS-L8 and found an increase of positive rate in DLB (61.9%) which is much higher than those in VaD (29.0%), AD (7.8%), or ND (2.6%).

Finally, in the HAICDDS project, we have continuously provided evidence that the combination of multiple standardized and structured questions is more powerful and can be optimized using artificial intelligence with machine learning techniques. This was the original idea behind the design of the HAICDDS questionnaire.

This study has several limitations. First, we used a single questionnaire for detecting FOS in patients with DLB and other forms of dementia; therefore, further studies using more tools are required to confirm the findings. Second, we used the original Taiwanese version of the questionnaire, which, although we translated to English, would call for a more precise and colloquial translation. Third, our study was conducted in only three centers in Taiwan. Therefore, the findings on the prevalence and association factors of FOS are not generalizable to all patients with DLB or other types of dementia.

Conclusion

In conclusion, our study showed that the informant-based single questionnaire FOSSQ can be a practical screening tool for the discrimination of DLB from ND or other types of dementia. The FOSSQ can be applied in clinical practice as well as in the dementia registration platform. Further machine learning techniques using artificial intelligence could improve the accuracy and efficiency of the questionnaire.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation, to any qualified researcher.

Ethics Statement

The studies involving human participants were reviewed and approved by the Show Chwan Memorial Hospital. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.

Author Contributions

P-YC undertook the literature search and data analysis, edited the Author Contributions, and was mainly responsible for revisions and drafts of the manuscript. M-CP participated in the data analysis and contributed to revisions and the final draft of the manuscript. G-UH undertook the literature search and contributed to revisions. C-YW contributed to revisions of the manuscript. R-CT undertook the literature search and contributed to revisions.

Funding

The study was funded by the Show Chwan Memorial Hospital No. RD-105032.

Conflict of Interest

P-YC work has been partly supported by the Show Chwan Memorial Hospital.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We would like to thank Prof. Shu-Hui Sue at National Taichung University of Science and Technology and Prof. Tsung-Lin Cheng at National Changhua University of Education for their feedback and suggestions during the experimental design and statistical analysis. Partial data and results of this study had been published as an abstract entitled “Freezing of Speech Single Questionnaire as a Screening Tool for Dementia with Lewy Bodies” in a poster section of the 2019 Alzheimer’s Association International Conference (AAIC).

References

Ackermann, H., Grone, B. F., Hoch, G., and Schonle, P. W. (1993). Speech freezing in Parkinson’s disease: a kinematic analysis of orofacial movements by means of electromagnetic articulography. Folia Phoniatr. 45, 84–89. doi: 10.1159/000266222

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, K. L., Xu, Y., Chu, A. Q., Ding, D., Liang, X. N., Nasreddine, Z. S., et al. (2016). Validation of the Chinese version of montreal cognitive assessment basic for screening mild cognitive impairment. J. Am. Geriatr. Soc. 64, e285–e290. doi: 10.1111/jgs.14530

PubMed Abstract | CrossRef Full Text | Google Scholar

Chiu, P. Y., Tang, H., Wei, C. Y., Zhang, C., Hung, G. U., and Zhou, W. (2019). NMD-12: a new machine-learning derived screening instrument to detect mild cognitive impairment and dementia. PLoS One 14:e0213430. doi: 10.1371/journal.pone.0213430

PubMed Abstract | CrossRef Full Text | Google Scholar

Cummings, J. L. (1988). Intellectual impairment in Parkinson’s disease: clinical, pathologic, and biochemical correlates. J. Geriatr. Psychiatry Neurol. 1, 24–36. doi: 10.1177/089198878800100106

PubMed Abstract | CrossRef Full Text | Google Scholar

Giladi, N., Kao, R., and Fahn, S. (1997). Freezing phenomenon in patients with parkinsonian syndromes. Mov. Disord. 12, 302–305. doi: 10.1002/mds.870120307

PubMed Abstract | CrossRef Full Text | Google Scholar

Giladi, N., McDermott, M. P., Fahn, S., Przedborski, S., Jankovic, J., Stern, M., et al. (2001). Freezing of gait in PD: prospective assessment in the DATATOP cohort. Neurology 56, 1712–1721. doi: 10.1212/wnl.56.12.1712

PubMed Abstract | CrossRef Full Text | Google Scholar

Gorelick, P. B., Scuteri, A., Black, S. E., Decarli, C., Greenberg, S. M., Iadecola, C., et al. (2011). Vascular contributions to cognitive impairment and dementia: a statement for healthcare professionals from the american heart association/american stroke association. Stroke 42, 2672–2713. doi: 10.1161/STR.0b013e3182299496

PubMed Abstract | CrossRef Full Text | Google Scholar

Hardy, C. J., Buckley, A. H., Downey, L. E., Lehmann, M., Zimmerer, V. C., Varley, R. A., et al. (2016). The language profile of behavioral variant frontotemporal dementia. J. Alzheimers. Dis. 50, 359–371. doi: 10.3233/jad-150806

PubMed Abstract | CrossRef Full Text | Google Scholar

Jellinger, K. A. (2018). Dementia with Lewy bodies and Parkinson’s disease-dementia: current concepts and controversies. J Neural Transm. 125, 615–650. doi: 10.1007/s00702-017-1821-1829

CrossRef Full Text | Google Scholar

Kosaka, K., Yoshimura, M., Ikeda, K., and Budka, H. (1984). Diffuse type of lewy body disease: progressive dementia with abundant cortical Lewy bodies and senile changes of varying degree–a new disease? Clin. Neuropathol. 3, 185–192.

PubMed Abstract | Google Scholar

Lawton, M. P., and Brody, E. M. (1969). Assessment of older people: self-maintaining and instrumental activities of daily living. Gerontologist 9, 179–186. doi: 10.1093/geront/9.3_Part_1.179

CrossRef Full Text | Google Scholar

Lin, C. M., Hung, G. U., Wei, C. Y., Tzeng, R. C., and Chiu, P. Y. (2018). An informant-based simple questionnaire for language assessment in neurodegenerative disorders. Dement. Geriatr. Cogn. Disord. 46, 207–216. doi: 10.1159/000493540

PubMed Abstract | CrossRef Full Text | Google Scholar

Lin, K. N., Wang, P. N., Liu, C. Y., Chen, W. T., Lee, Y. C., and Liu, H. C. (2002). Cutoff scores of the cognitive abilities screening instrument. Chinese version in screening of dementia. Dement. Geriatr. Cogn. Disord. 14, 176–182. doi: 10.1159/000066024

PubMed Abstract | CrossRef Full Text | Google Scholar

Louis, E. D., Winfield, L., Fahn, S., and Ford, B. (2001). Speech dysfluency exacerbated by levodopa in Parkinson’s disease. Mov. Disord. 16, 562–565. doi: 10.1002/mds.1081

PubMed Abstract | CrossRef Full Text | Google Scholar

Macht, M., Kaussner, Y., Moller, J. C., Stiasny-Kolster, K., Eggert, K. M., Kruger, H. P., et al. (2007). Predictors of freezing in Parkinson’s disease: a survey of 6,620 patients. Mov. Disord. 22, 953–956. doi: 10.1002/mds.21458

PubMed Abstract | CrossRef Full Text | Google Scholar

Mao, H. F., Chang, L. H., Tsai, A. Y., Huang, W. W., Tang, L. Y., Lee, H. J., et al. (2018). Diagnostic accuracy of instrumental activities of daily living for dementia in community-dwelling older adults. Age Ageing 47, 551–557. doi: 10.1093/ageing/afy021

PubMed Abstract | CrossRef Full Text | Google Scholar

McKeith, I. G., Boeve, B. F., Dickson, D. W., Halliday, G., Taylor, J. P., Weintraub, D., et al. (2017). Diagnosis and management of dementia with Lewy bodies: fourth consensus report of the DLB Consortium. Neurology 89, 88–100. doi: 10.1212/wnl.0000000000004058

PubMed Abstract | CrossRef Full Text | Google Scholar

McKeith, I. G., Dickson, D. W., Lowe, J., Emre, M., O’Brien, J. T., Feldman, H., et al. (2005). Diagnosis and management of dementia with lewy bodies: third report of the DLB consortium. Neurology 65, 1863–1872. doi: 10.1212/01.wnl.0000187889.17253.b1

PubMed Abstract | CrossRef Full Text | Google Scholar

McKhann, G. M., Knopman, D. S., Chertkow, H., Hyman, B. T., Jack, CRJr, Kawas, C. H., et al. (2011). The diagnosis of dementia due to Alzheimer’s disease: recommendations from the National Institute on Aging-Alzheimer’s association workgroups on diagnostic guidelines for Alzheimer’s disease. Alzheimer’s Dement. 7, 263–269. doi: 10.1016/j.jalz.2011.03.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Morris, J. C. (1993). The clinical dementia rating (CDR): current version and scoring rules. Neurology 43, 2412–2414. doi: 10.1212/wnl.43.11.2412-a

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, H. K., Yoo, J. Y., Kwon, M., Lee, J. H., Lee, S. J., Kim, S. R., et al. (2014). Gait freezing and speech disturbance in Parkinson’s disease. Neurol. Sci. 35, 357–363. doi: 10.1007/s10072-013-1519-1511

PubMed Abstract | CrossRef Full Text | Google Scholar

Vercruysse, S., Gilat, M., Shine, J. M., Heremans, E., Lewis, S., and Nieuwboer, A. (2014). Freezing beyond gait in Parkinson’s disease: a review of current neurobehavioral evidence. Neurosci. Biobehav. Rev. 43, 213–227. doi: 10.1016/j.neubiorev.2014.04.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: freezing of speech, fluctuating cognition, dementia with Lewy bodies, Alzheimer’s disease, vascular dementia

Citation: Chiu P-Y, Hung G-U, Wei C-Y, Tzeng R-C and Pai M-C (2020) Freezing of Speech Single Questionnaire as a Screening Tool for Cognitive Dysfunction in Patients With Dementia With Lewy Bodies. Front. Aging Neurosci. 12:65. doi: 10.3389/fnagi.2020.00065

Received: 15 November 2019; Accepted: 25 February 2020;
Published: 28 April 2020.

Edited by:

Jiehui Jiang, Shanghai University, China

Reviewed by:

Zhihua Yu, Shanghai University of Traditional Chinese Medicine, China
Jung Lung Hsu, Chang Gung Memorial Hospital, Taiwan
Can Sheng, Capital Medical University, China

Copyright © 2020 Chiu, Hung, Wei, Tzeng and Pai. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ming-Chyi Pai, pair@mail.ncku.edu.tw

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.