Korean Speech-Language & Hearing Association(KSHA)

Editorial Board

Korean Speech-Language & Hearing Association(KSHA) - Vol. 29 , No. 3

Journal of Speech-Language & Hearing Disorders - Vol. 29, No. 3, pp.17-26
Abbreviation: JSLHD
ISSN: 1226-587X (Print) 2671-7158 (Online)
Print publication date 31 Jul 2020
Received 10 Jun 2020 Revised 10 Jul 2020 Accepted 28 Jul 2020
DOI: https://doi.org/10.15724/jslhd.2020.29.3.017

A Preliminary Study of the Resting-State Speech Rate Network in Patients With Parkinson’s Disease
Sun Woo Kim1, *
1Dept. of Speech of Language Rehabilitation, Suncheon Jeil College, Professor

말속도 관련 파킨슨병 환자의 휴식상태 기능적 연결망 예비연구
김선우1, *
1순천제일대학교 언어치료과 교수
Correspondence to : Sun Woo Kim E-mail : swkim@suncheon.ac.kr

Copyright 2020 ⓒ Korean Speech-Language & Hearing Association.
This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Studies on the rate of speech in patients with Parkinson’s disease (PD) report various results. Some results show slower speech rate in patients with PD than in normal controls (NC), while others report an increased rate of speech in these; others still, reveal no differences between the NC and PD groups. Despite our understanding of the sites primarily responsible for speech production in NC, alteration of the functional connectivity (FC) in patients with PD still remains unclear. The aim of this study was to map the speech rate-dependent neural connections using resting-state (rs) FC techniques.


This study included 14 patients with PD and 10 NC. After testing diadochokinetic rate, all participants underwent rs functional magnetic resonance imaging (fMRI) scanning. We then selected four seeds in each subcortical region based on prior fMRI studies, especially the basal ganglia and cerebellum.


Compared with the NC group, all the seed regions of interest (ROIs) in the PD group, except the left putamen and right caudate nucleus, showed significantly decreased or increased FC with the cortical and subcortical areas. Among these ROIs, only the left cerebellum (lobule VI) exhibited significantly increased FC with the right inferior parietal lobule in the PD group. While functional connectivity is altered, the speech performance in patients with PD remained similar to that of the NC group.


Using the rs fMRI technique, we provided evidence that the left cerebellum is strongly interconnected with the right cerebral cortex in patients with PD. We propose that activation of the cerebellum participates in the compensatory mechanism which underlies the lack of statistically significant difference in speech rate when patients with PD are compared with NC, although overall FC decreases.


파킨슨병(Parkinson’s disease: PD)으로 인해 발현되는 운동저하형 마비말장애(hypokinetic dysarthria)는 구어를 사용한 의사소통 능력을 감소시켜 환자의 삶의 질을 저하시키는데, PD에서 기인된 마비말장애는 타 마비말장애에서는 관찰하기 힘든 이질적인 말속도 유형(느려진, 빨라진 혹은 변화 없는 말속도)이 집단 내에서 존재한다. 전통적으로 기저핵 이상이 PD 관련 운동 문제의 원인으로 알려져 왔지만 근래에 이루어진 뇌영상 연구는 소뇌 관련성을 점차적으로 강조하고 있다. 이에 파킨슨병 환자의 말속도 변화를 기저핵뿐만 아니라 소뇌를 포함시켜 살펴볼 필요성이 제기된다.


약물이 효과적으로 작용하는 상태의 파킨슨병 환자 14명(남자 : 여자=8 : 6)과 정상 통제군 10명(남자 : 여자=4 : 6)의 뇌영상을 3.0 테슬라를 사용하여 휴식 상태에서 획득한 뒤 말속도 조절에 관여하는 주요 피질하 영역(기저핵; 꼬리핵의 머리, 조가비핵, 소뇌; VI, VIIIA)으로 알려진 곳을 관심영역(region of interests: ROIs)으로 지정하여 전체 뇌에서 군 간의 기능 연결성을 확인하였다. 그리고 교호운동속도(diadochokinetic rates: DDK rates) 과제인 교대운동속도(alternating motion rates: AMRs)와 일련운동속도(sequential motion rates: SMRs)를 실시하여 두 집단 간의 말속도를 비교하였다.


첫째, 집단 간 비교에서 환자군은 왼쪽 소뇌 VI-오른쪽 하두정엽을 제외한 뇌 전반에서 통제군에 비해 기능적 활성화가 유의미하게 저하되었다. 둘째, DDK 과제에서 두 집단 간의 말속도는 통계적으로 유의미한 차이가 없었다.


전반적으로 저하된 뇌 기능에도 불구하고 파킨슨병 환자군이 보여준 정상군과 유사한 수준의 말속도 수행은 발병 후 변화 없는 말속도를 보이는 환자군의 경우는 기능적 연결성이 증가한 왼쪽 소뇌와 오른쪽 하두정엽의 작용에 따른 결과일 가능성이 제기되었다.

Keywords: Parkinson’s disease, speech rate, resting-state functional magnetic resonance imaging, cerebellum, basal ganglia
키워드: 파킨슨병, 말속도, 휴식상태 뇌기능자기공명영상, 소뇌, 기저핵

Ⅰ. Introduction

Speech is one of the most intricate and motoric human behaviors with respect to the involved neural networks. Although brain areas related to speech production have been well-investigated in normal subjects (Eickhoff et al., 2009; Guenther et al., 2006; Price, 2012; Simonyan & Fuertinger, 2015), our understanding of altered neural networks originated from the basal ganglia pathology in patients with PD still remains unclear. Traditionally, sequences of the events involved in speech production, such as planning, programming, and execution, were thought to be controlled mainly by the cerebral cortex, with the subcortical areas playing a minor role in the selection of desired movements and / or the inhibition of unwanted movements (Albin et al., 1989; Mink, 1996).

However, over the past 20 years, such a distinct separation of roles of the brain structures in controlling speech production has been challenged by new information. Using various brain imaging technologies, the interconnection between the cortical and subcortical areas to control of speech motor, especially the basal ganglia and cerebellum, have been highlighted (Bohland & Guenther, 2006; Riecker et al., 2005; Wildgruber et al., 2001). Neuroimaging studies on normal speech motor control have delineated a “minimal network for overt speech production” including the mesiofrontal structures (supplementary motor area and anterior cingulate gyrus), bilateral pre- and post- central convolutions, extending rostrally into posterior parts of the inferior frontal gyrus of the language-dominant hemisphere and left anterior insula as well as bilateral components of the basal ganglia, cerebellum, and thalamus (Bohland & Guenther, 2006).

However, despite our understanding of the sites primarily responsible for speech production in normal subjects, alteration of the functional network in patients with PD still remains unclear. Although often veiled by the more prominent and distressing skeletal aspects such as gait and upper limb control, speech impairment is a very frequent symptom in PD. It is estimated that approximately 70% (Hartelius & Svensson, 1994), with some estimates reaching as high as 90% (New et al., 2015; Ramig et al., 2011), patients with PD undergo a disruption of speech motor control known as “hypokinetic dysarthria”. During disease progression, hypokinetic dysarthria can emerge at all stages of the disease, and generally worsens as the disease progresses, causing a progressive loss of communication abilities and increasing isolation from society (Pinto et al., 2004; Skodda, 2011).

Results of similar studies have demonstrated that patients with PD show abnormalities in voice production, so-called “hypophonia”; however, data concerning speech rate in these patients is insufficient and inconsistent. Studies on the rate of speech report various results, with some reporting slower speech rate in patients with PD than in normal speakers (Dworkin & Aronson, 1986; Hammen & Yorkston, 1996; Ludlow et al., 1987), while others report an increased rate of speech in these patients (Ackermann et al., 1995; Hirose et al., 1982; McRae et al., 2002), and yet others reveal no differences between the control and PD groups (Canter, 1965; Lowit et al., 2006; Skodda et al., 2011).

Traditionally, the classical model of PD (cortico-basal ganglia-thalamo-cortical loops) accentuated the function of the basal ganglia in the cardinal symptoms and axial features associated with PD. However, other changes in motor symptoms, such as speech, cannot be interpreted solely based on basal ganglia dysfunction. Limitations in the current hypothesis led us to believe that a large amount of evidence from experimental studies could be analyzed to delineate and understand ambiguous speech symptoms.

Previous resting-state (rs) studies on speech impairment in PD have mainly focused on the basal ganglia; therefore, we sought to investigate whether FC within the cerebellum might also be linked to speech rate impairment. Basal ganglia pathology may show that changes in the FC between basal ganglia structures and the cerebellum may also be involved in speech rate impairment in PD. While several studies have identified abnormal rs connections in the basal ganglia or at the cortical levels in PD, it remains unclear whether speech rate impairment in PD involves connectivity changes in the cerebellum. Furthermore, only a few studies have been conducted to assess neural connections based on connectivity in speech rate networks.

Our goal in this study was to map the speech rate-dependent neural connections using rs FC techniques. Rs networks are associated with self-oriented mental activity and offer a means of evaluating the status of functional systems within the brain, without external goal-directed cognitive performance. Therefore, the use of rs networks analysis may be advantageous for the identification of brain regions functionally involved in the pathological changes in neurodegenerative diseases (Filippi et al., 2018; Fox & Greicius, 2010). Thus, we performed a comparative analysis of rs FC in patients with PD and normal controls (NC) to further elucidate cerebellum-related alteration of FC.

Ⅱ. Methods
1. Participants

This study included 14 patients diagnosed with PD (men : women=8 : 6) and 10 healthy NC (men : women=4 : 6) who were recruited from a university hospital in Seoul between February and December of 2016. Diagnosis of PD was performed according to the clinical diagnostic criteria of the UK PD Society Brain Bank, and all participants’ native language was Korean.

Before the functional image acquisition, all participants were screened using cognition, depression, and language tests. The purpose of this study was to compare rs fMRI networks based on speech rate; therefore, factors that might negatively affect or influence speech rate needed to be controlled for before acquiring brain images. All participants who underwent fMRI scanning were found to be within the normal range (above the cut-off point based on years of education and age) on the Korean version of the Montreal Cognitive Assessment (K-MoCA, Kang et al., 2009), with a score < 16 on the Korean version of the Geriatric Depression Rating Scale (GDS-K, Cho et al., 1999), within 1 standard deviation (SD) of the Korean version of the Boston Naming Test (K-BNT, Kim & Na, 1997), and within 1 SD of Paradise Korean version of Western Aphasia Battery (PK-WAB, Kim & Na, 2012). To compare demographic characteristics of the two groups, the Mann-Whitney U-test and chi-squared (χ2) tests were used for continuous and categorical variables, respectively. Table 1 summarizes the demographic features of patients with PD and NC. No significant differences were found in age, sex, aphasia quotient, K-BNT, K-MoCA, and GDS-K scores between the PD and NC groups, except for years of education.

Table 1. 
Subject characteristics for PD and NC group
PD (n=14) NC (n=10) p
Age (Yr.) 67.35 ± 7.30 65.40 ± 4.19 .678
Male sex (%) 8 (57.1%) 4 (40%) .408
Education (Yr.) 14.50 ± 4.55 13.70 ± 2.58  .024
POT (Yr.) 10.50 ± 5.54 N/A -
M-H & Y  2.35 ± 0.56 N/A -
PK-WAB AQ 97.14 ± 1.70 96.58 ± 2.85 .680
K-BNT 51.64 ± 4.39 52.50 ± 6.58 .408
K-MoCA 25.21 ± 2.48 25.70 ± 3.05 .408
GDS-K  8.42 ± 5.69  4.40 ± 3.94 .214
Note. Results are presented as mean ± standard deviation. PD=Parkinson’s disease; NC=normal controls; Yr.= years; POT=post-onset time; N/A=not applicable; M-H & Y=modified Hoehn & Yahr Scale; PK-WAB=Paradise Korean version of the Western Aphasia Battery; AQ=aphasia quotient; K-BNT= Korean version of the Boston Naming Test; K-MoCA= Korean version of the Montreal Cognitive Assessment; GDS-K=Korean version of the Geriatric Depression Rating Scale.

We received approval form the Yonsei University Severance Hospital ethical standards committee on human experimentation for experiments involving human subjects (IRB No. 4-2015-0843). Written informed consent was obtained from all the subjects who participated in this study.

2. Procedures
1) Acquisition of speech rate data

Speech data was acquired using diadochokinetic (DDK) rates. The DDK rates are composed of two types of rates: alternating motion rates (AMRs) and sequential motion rates (SMRs). Syllable repetitions, performed as fast as possible, have been demonstrated to be a valid test of maximum speaking rates, and have a potential relationship with speaking rates in more complex speech tasks, such as reading or conversation (Wang et al., 2004). Participants who produced rapid DDK rates at the expense of precision were instructed to speak as fast as possible without being imprecise. Each subject performed each task three times in a random order.

The speech recording procedure was as follows. All patients in the PD group were in “ON” medication state (Madhyastha et al., 2015; Martínez-Sánchez et al., 2016; New et al., 2015; Skodda, 2011). Because the aim of this study was to identify the brain functional network involved in speech production, and previous fMRI and perceptual evaluation studies have shown speech production to be similar with and without medication (Maillet et al., 2012; Skodda et al., 2011; Skodda et al., 2011; Skodda et al., 2010). Generally, patients with PD receive their medicine 3~4 times a day when they are awake; therefore, speech communication occurs only during the “ON” state. The speech samples were obtained using an electret condenser microphone (ECM-MS 908C; Sony, Japan) placed on a microphone stand approximately 10~15 cm from each participant’s mouth at 15°. The microphone was connected to a linear PCM-M10 recorder (Sony, Japan), and the acoustic signal was recorded at a sampling rate of 44.1 kHz, with 16-bit quantization.

2) Analysis of speech rate date

We captured 3 stable seconds from the overall duration (5 seconds) of the speech task using the Computerized Speech Lab (model 4150B; KayPENTAX, Lincoln Park, USA). If slurred speech was included in the 3 seconds, a spectrogram was used to determine a syllable; if it was not made up of a consonant-vowel (e.g., a consonant without a vowel or a vowel without a consonant), it was not counted as one syllable (Figure 1).

Figure 1. 
An example of acoustic analysis of a patient with Parkinson’s disease for selecting 3 stable seconds (two blue lines) in /puh/ alternate motion rate (among four slurred syllables, only one slurred syllable was included in the analysis) using Computerized Speech Lab

3) Acquisition of fMRI data

All participants underwent fMRI scanning with a 3.0-Tesla MRI scanner (Achieva, Philips Medical System, Best, Netherlands) to obtain T2*-weighted single-shot echo planar imaging sequences. Each participant was axially scanned using the following parameters: voxel size, 2.8 × 2.8 × 3.0 mm3; slice number, 31 (interleaved); matrix, 80 × 80; slice thickness, 3.0 mm; gap, 1.0 mm; repetition time, 2000 ms; echo time, 30 ms; flip angle=90°; and field of view, 220 mm. Each 330-second scan produced 165 fMR images. Earplugs were offered to the subjects to reduce the scanner noise. The subjects were instructed to remain awake and still, keep their eyes closed, and not focus on a specific thought. During the routine questioning performed immediately after the examination, none of the participants reported having fallen asleep (van den Heuvel & Hulshoff Pol, 2010).

4) Processing of fMRI data

Preprocessing of the fMRI data was conducted using the Analysis of Functional NeuroImages (https://afni.nimh.nih.gov/afni) software. To stabilize the magnetic field, the initial five volumes of each rs fMRI datum were excluded. The remaining fMRI data were processed in the following order: despiking, slice-timing, and head motion correction. Prior to the normalization of fMRI data to the common space, co-registration between anatomical T1 image and fMRI data was performed using the affine transform with Local Pearson Correlation cost function (Saad et al., 2009). Further, eroded white matter (WM) and large ventricle (LV) masks were registered to fMRI data using the same transform matrix. The fMRI data, anatomical T1 image, and masks in the native space were normalized to the common space using the standard Montreal Neurological Institute (MNI) 152 template with an isotropic voxel size of 2 mm. In addition, fMRI data were spatially blurred using a 6-mm full width at half maximum Gaussian kernel.

After spatial normalization, the fMRI data were corrected by nuisance-removal regression using the anatomy-based correlation corrections method (Jo et al., 2010). which is a regression model for extracting the nuisance signal of specific tissues, such as the WM and LV. It is assumed that the actual brain signal is generated from the gray matter. In order to avoid mixing signals from different tissues, anatomy-based regressors were created before spatial smoothing. The regressors of the anatomy-based correlation corrections method were as follows: (1) six parameters from the head motion correction, (2) locally (r=15 mm) averaged signal from the eroded WM mask, and (3) averaged signal from the eroded LV mask. The nuisance regression model was applied using censoring and bandpass filtering together. The censoring was applied to fMRI volumes with the Euclidean norm of the first derivative of head motion greater than .25. The bandpass filtering was applied to fMRI data with .009 < f < .08 to deduct physiological noise.

5) Analysis of functional connectivity

As we were interested in the key brain regions controlling speech rate, we selected four seed regions of interest (ROIs) in each hemisphere which were based on previous studies on speech production (Brown et al., 2009; Chang et al., 2009; New et al., 2015): (1) the putamen, (2) head of the caudate nucleus (3) lobule VI, and (4) lobule VIIIA of the cerebellum (Table 2). The averaged signal of each ROI was used as the reference signal. Each ROI correlation map was calculated using Pearson’s correlation coefficient with a reference signal for the whole brain. The correlation map for each subject was converted to a z-score map using Fisher’s r-to-z transformation.

Table 2. 
Seed ROIs
Brain ROI Side BA x y z
Basal ganglia Putamen Left N/A -15   6  8
Right N/A 20   8  2
Caudate nucleus (head) Left N/A -6  -1 10
Right N/A 13  -2 15
Cerebellum Cerebellum (lobule VI) Left N/A -36 -55 -32
Right N/A 27 -64 -21
Cerebellum (lobule VIIIA) Left N/A -12 -72 -50
Right N/A 24 -66 -50
Note. N/A=not applicable; ROI=regions of interest; BA=Brodmann area.

3. Statistical Analysis
1) Speech rate data

To compare the number of syllables per second (SPS) of DDK between the two groups, a Mann-Whitney U-test was conducted. Statistical analyses were performed using SPSS 23.0 software, and the significance level was set at .05 for all statistical analyses.

2) fMRI data

For comparison of FC between the two groups, a two-sample t-test was used while controlling for the effects of age and sex as covariates. To obtain the significance level combination of uncorrected individual voxel p-value and cluster size, Monte Carlo simulation was conducted to control for Type I errors, using the AlphaSim program (parameters: uncorrected individual voxel p-value=.02, simulation=10,000 times, 8-mm full width at half maximum Gaussian filter with a whole-brain mask (Poline et al., 1997). The two-sample t-test was corrected by p<.05 level (uncorrected individual voxel height threshold of p<.02, with a minimum cluster size of 307 voxels). Furthermore, to determine whether the observed FC could be used to discriminate between each group, Spearman’s partial correlations were used after controlling for age, sex, and years of education.

Ⅲ. Results
1. Functional Connectivity

Direct mean comparisons demonstrated that the patients with PD in “ON” medication state had decreased whole-brain FC (Table 3), i.e., between the basal ganglia and cerebral cortex (right putamen-left inferior parietal lobule and left head of caudate-left lingual gyrus), cerebellum and cerebral cortex (left cerebellum [lobule VI]-right cuneus, right cerebellum [lobule VI]-left superior temporal gyrus, right cerebellum [lobule VI]-right precentral gyrus, right cerebellum [lobule VI]-right postcentral gyrus, right cerebellum [lobule VI]-right precuneus, left cerebellum [lobule VIIIA]-right precentral gyrus, right cerebellum [lobule VIIIA]-right medial frontal gyrus, right cerebellum [lobule VIIIA]-left posterior cingulate gyrus), basal ganglia and cerebellum (left head of the caudate nucleus-right declive), and within the cerebellum (left cerebellum [lobule VI]-right declive, right cerebellum [lobule VI]-left culmen, and right cerebellum [lobule VIIIA]-left cerebellar tonsil), except the left cerebellum [lobule VI]-right inferior parietal lobule connection, compared with the controls.

Table 3. 
Resting-state functional connectivity of the basal ganglia and cerebellum between-group
MNI coordinates
Seed Group Brain region Side x y z t-value voxels
Lt. putamen PD=NC N/A
Rt. putamen PD<NC Inferior parietal lobule Lt. -46 -62 46 3.771 352
Lt. caudate nucleus (head) PD<NC Lingual gyrus Lt. -2 -72 -8 5.115 366
Declive Rt. 26 -88 -30 3.919 312
Rt. Caudate nucleus (head) PD=NC N/A
Lt. cerebellum (lobule VI) PD<NC Cuneus Rt. 4 -64 6 4.751 581
Decilve Rt. 34 -78 -22 5.289 458
PD>NC Inferior parietal lobule Rt. 36 -38 40 -4.280 312
Lt. cerebellum (lobule VIIIA) PD<NC Precentral gyrus Rt. 48 -14 46 4.761 401
Rt. cerebellum (lobule VI) PD<NC Culmen Lt. -8 -68 -16 7.333 795
Superior temporal gyrus Lt. -66 -10 4 6.307 481
Postcentral gyrus Rt. 60 -32 44 7.977 414
Precentral gyrus Rt. 56 -4 16 4.694 394
Precuneus Rt. 12 -54 46 6.241 380
Rt. cerebellum (VIIIA) PD<NC Medial frontal gyrus Rt. 12 -24 50 4.580 868
Cerebellar tonsil Lt. -24 -32 -40 4.693 427
Posterior Cingulate gyrus Lt. -16 -28 46 5.969 340
Note. Lt.=left; Rt.=right; N/A=not applicable; PD=Parkinson’s disease; NC=normal controls; MNI=montreal neurological institute.

2. DDK Rate

The median of SPS in the PD group measured was: 6.33 (interquartile range [IQR]: 1.37), 6.33 (IQR: 1.75), and 6.16 (IQR: 1.33) for /puh/, /tuh/, and /kuh/, respectively, while that for the NC group was: 6.83 (IQR: 1.17), 6.50 (IQR: .75), and 6.33 (IQR: .75) for /puh/, /tuh/, and /kuh/, respectively (Table 4). There was no significant difference between the two groups (p >.05). When comparing the median SMRs, the performance for /puhtuhkuh/ between the PD (median: 2.36, IQR: .67) and NC (median: 2.25, IQR: .41) groups was not statistically significantly different (p >.05, Table 5).

Table 4. 
Comparison of alternate motion rates (syllables per second) between PD and NC groups
Median IQR Median IQR
/puh/ 6.33 1.37 6.83 1.17 .406
/tuh/ 6.33 1.75 6.50  .75 .413
/kuh/ 6.16 1.33 6.33  .75 .314
Note. AMRs=alternate motion rates; PD=Parkinson’s disease; NC=normal controls; IQR=interquartile range.

Table 5. 
Comparison of sequential motion rates (syllables per second) between PD and NC groups
Group Median IOR p
PD 2.36 .67 .419
NC 2.25 .41
Note. PD=Parkinson’s disease; NC=normal controls; IQR=interquartile range.

Ⅳ. Discussion

Speech is one of the most intricate and motoric human behaviors with respect to the involved neural networks. Although brain areas related to speech production have been well-investigated in normal subjects (Eickhoff et al., 2009;Guenther et al., 2006; Price, 2012; Simonyan & Fuertinger, 2015), our understanding of altered neural networks originated from the basal ganglia pathology in patients with PD still remains unclear. We used seed-based interregional correlations of rs fMRI data and investigated the functional interaction of the key brain regions related to speech rate, i.e., the putamen, head of the caudate nucleus, and cerebellum (lobules VI and VIIIA).

Compared with the NC group, all the seed ROIs in the PD group, except the left putamen and right caudate nucleus, showed significantly decreased or increased FC with the cortical and subcortical areas. Among these ROIs, only the left cerebellum (lobule VI) exhibited significantly increased FC with the right inferior parietal lobule in the PD group. This finding is consistent with previous studies showing that the brain function of patients with PD under dopaminergic medication is globally reduced compare with normal subjects (Berding et al., 2001; Festini et al., 2015; Maillet et al., 2012; New et al., 2015). This result highlights the fact that medication does not restore the FC in patients with PD to the normal state (Maillet et al., 2012). Nevertheless, this study results demonstrate that there is no difference in the median scores of speech parameters (i.e., AMRs, SMRs) when patients with PD are compared with NC. Although there were no relevant differences between the two groups, all the speech parameters presented a higher IQR in patients with PD.

One interpretation of this result is a cerebellar compensatory phenomenon to preserve speech rate in PD. The cerebellum and basal ganglia are the two major subcortical structures that influence multiple aspects of motor behavior (Strick et al., 2009). Both structures form multi-synaptic loops; moreover, substantial interactions exist between these structures, which are linked together to produce an integrated function (Bostan & Strick, 2010; Houk & Wise, 1995; Wu & Hallett, 2013). In particular, the cerebellum is thought to act a core role in the formation of internal representations for actions that allow us to execute precise temporal coordination, online sequencing, and smooth motor responses (Ackermann, 2008; Ackermann et al., 2007; Ito, 2008; Manto et al., 2012; Moberget & Ivry, 2016; Ramnani, 2006). Within the speech production system, one of the main functions of the cerebellum is to control the regulation of the ongoing temporal sequencing, not only during overt speaking but also the generation of the prearticulatory verbal cord in covert or silent speech production (Callan et al., 2006; Gordon, 1996; Simonyan & Fuertinger, 2015).

Additionally, as previously mentioned, compared with the NC group, the PD group had significantly increased strength of FC between the left cerebellar lobule VI and right inferior parietal lobule. A recent study suggested that the function connection between the cerebellum and inferior parietal lobule plays critical roles in the formation of the speech production network (Simonyan & Fuertinger, 2015). The inferior parietal lobule is known to be involved in phonological processing (Hickok & Poeppel, 2007), monitoring the onset of speech (Kort et al., 2014), and guiding of movement via sensory feedback (Mattingley et al., 1998), which may be critical to facilitate the transition from the resting state to speaking (Simonyan & Fuertinger, 2015) and to execute speech production (Hallett & Grafman, 1997).

Another interpretation considers the inferior parietal lobule to be a primary region for sensorimotor integration, functioning as an “association cortex”. Patients of PD exhibit sensorimotor integration impairments from the early stage of the disease. Thus, the hyper-activity of the inferior parietal lobule might be a strategy to compensate for impaired processing of the somatosensory input via the pathologically affected basal ganglia toward the motor cortex (Tahmasian et al., 2017).

In using the Rs fMRI technique, we provided evidence that the PD subjects exhibited a significant decrease in functional connectivity than the NC group and proved the specific cerebellum area was associated with speech rate control. The results would provide a better understanding of the disease and provide information for the development of new treatment approaches.


This work was supported by the Ministry of Education of the Republic of Korea and the National Research Foundation of Korea (No. NRF-2015S1A5A8017149).

이 논문은 2015년 대한민국 교육부와 한국연구재단의 지원을 받아 수행된 연구임(No. NRF-2015S1A5A8017149).

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