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1. Introduction
Patients after stroke who have both upper extremity (UE) motor impairment and/or language dysfunction are common [1]. These two types of poststroke dysfunction are the most apparent neuropsychological deficits occurring after stroke: UE motor deficit occurs in about 80% of stroke survivors, aphasia in 21%-38%, and cooccurrence in about 24% [2–4]. PSA with UE motor dysfunction impacts social participation and quality of life, and it can also be associated with multiple comorbidities and lead to worse prognosis [5, 6]. Due to the adjacent anatomical location, ischemia or hemorrhage in the middle cerebral artery (MCA) often leads to UE motor dysfunction and nonfluent aphasia. Nevertheless, there are small samples of study that have analyzed the relationship between hand-arm motor dysfunction and aphasia using lesion volume and location as control variables, showing that the association is not determined by anatomical relationships alone. The extents and limitations of UE and language cortical reciprocity remain under debate; it is likely that UE movement and language have shared neural correlates not merely depending on anatomical proximity and vascular factors.
In Huashan Hospital, there is an original operation, a contralateral seventh cervical nerve transfer to improve UE motor function in patients with chronic central injury [7]. After the surgery, we found that patients with PSA not only improved their UE motor status but also their language function. These phenomena suggest a deep neural mechanism relationship between language function and UE motor status after stroke. Several studies [8–11] have focused on the potential relationship between UE motor status and language function. From a human evolution perspective, language was spurred by freedom of hand movement as an additional consequence of this upright posture. Gestures are a combination of UE movements and language [12]. A retrospective cohort study addressed the possible interaction between motor impairment and aphasia recovery after stroke. Motor responders showed better linguistic performances at the final aphasia assessment than motor nonresponders, while language responders reached a higher level of motor functioning than language nonresponders [8]. Meanwhile, a significant response in one domain was not associated with any deterioration in the other. Furthermore, Harnish et al. examined five patients with aphasia and hemiparesis poststroke during six weeks of UE therapy but not receiving speech therapy. Patients were assessed not only for the UE motor recovery but also for changes in their language abilities. fMRI data demonstrated shifts in increased blood oxygen improvements in both UE motor status and language function scores [13]. However, current studies rarely focus on simultaneous UE motor dysfunction with language deficits and even less on both functions’ concurrent recovery during stroke recovery. Most studies only unexpectedly found this phenomenon or were mostly exploratory paradigm intervention studies [1, 14–16]. Few studies have focused on the difference in UE motor function status between patients with PSA and nonphasic poststroke patients. Moreover, no study provides evidence on the correlation between UE motor status and language function after stroke [8, 9], which leads to low attention to UE-language correlation so that UE and speech-language therapies are completely separated during UE motor and (or) speech rehabilitation.
To cover this gap, the present study investigated the UE motor status and language function of stroke patients by a cross-sectional investigation. We hypothesized that there were differences in motor status between stroke patients with PSA and without PSA and that there were some relationships between the speech-language function and UE motor status in patients with PSA.
Therefore, the objectives of this study were (1) to compare the UE motor status between patients with PSA and without PSA, (2) to investigate the association between language function and UE motor status in patients with PSA, and (3) based on (2), to determine which dimension of PSA evaluation is most closely related to the UE motor status.
2. Methods
2.1. Study Population and Design
This study was conducted between May 2020 and June 2021 in the departments of rehabilitation medicine of six hospitals from different regions in China. Patients were consecutively screened for the following criteria: (1) aged 18 years or older; (2) native Chinese speaker, (3)
Patients were evaluated in a single test session performed by speech therapists and occupational therapists who had received consistency training. One trained researcher performed the data collection. Patients’ baseline characteristics were evaluated, including age at stroke onset, gender, comorbidities, hand dominance, time poststroke, lateralization, and stroke type. After 2326 patients were screened, those who met the above conditions participated in this study, 214 among whom with PSA were in the observational PSA group. A group of 221 patients without PSA after stroke matched for age and sex participated and were distributed into the non-PSA group as controls. The sample sizes were estimated referring to other similar studies [8, 17, 18]. As an important outcome, the UE motor impairment and function between the two groups were compared. Further evaluation was done in the observational PSA group to see the association between UE motor status and language function evaluation scores. For further validation purposes, the relationships between them were analyzed by multiple linear regression. Then, to observe the difference between different time periods from stroke onset, subsequent stratification analyses by time (1-3 months, 4-6 months, and >6 months) were performed. Our study used a cross-sectional observational design. The ethics committee approved the study protocol of Huashan Hospital of Fudan University and all participating centers according to the 1964 Declaration of Helsinki’s ethical standards and its later amendments. This trial is registered with ChiCTR2000033792. All patients or their families provided written informed consent before study enrollment.
2.2. Measurement Instruments and Evaluation
2.2.1. Evaluation of PSA: Aphasia Quotient of Western Aphasia Battery-Revised (WAB-AQ) and Boston Diagnostic Aphasia Examination (BDAE)
PSA was evaluated using the Chinese version of WAB-AQ, a commonly used clinical evaluation of PSA that assesses the presence, type, and severity of aphasia with a 0-100 scale (
2.2.2. Evaluation of UE Motor Impairment: Fugl-Meyer Assessment for the Upper Extremity (FMA-UE)
The FMA was used to assess extremity motricity, balance, some sensory details, and joint dysfunction in hemiplegic patients. We evaluated the only motor function of the UE, including measurement of voluntary movement, velocity, coordination, and reflex activity. A total of 33 items are included. A 3-step (0-1-2) ordinal scale is applied to each item (0 = details cannot be performed; 1 = details are performed only partly; 2 = details are performed throughout the full range of motion of the joint). This gives a total maximum score of 66, which defines a normal motor function (42 and 14 for the arm and hand, respectively). FMA-UE mainly aims at evaluating UE motor impairment and dysfunction after stroke.
2.2.3. Evaluation of UE Motor Function: Action Research Arm Test (ARAT)
Instruments needed to perform the test are as follows: woodblocks, a ball, a washer and bolt, a stone, two different sizes of alloy tubes, two glasses, a marble, and a 6 mm ball bearing (instrument model: OT-KL-40400). The test is a 4-grade scale ranging from 0 to 3 with a
2.3. Statistical Analysis
Data were analyzed with IBM SPSS Statistics version 26.0. Demographics and clinical variables, presented as
3. Results
3.1. Demographics
From a total of 2326 patients, we excluded 1891, leaving 435 patients for analysis (see Figure 1). 435 patients underwent a complete systematic assessment with a median course of 15 weeks (IQR: 7-32). The median age of the patients was 60.6 years (
[figure omitted; refer to PDF]
Our results provide compelling evidence for the relation between UE motor status and language function in terms of behavioral performances and demonstrate that this relationship can be applied to patients’ therapy with PSA or UE motor deficit or both after stroke. Patients with PSA have worse hand and UE motor status, which calls for more attention to be given to UE motor rehabilitation in these patients. Interactions between the auditory system and the motor system are related to speech perception. The motor theory of perception has two basic claims: perceiving speech is perceiving gestures and perceiving speech involves the motor system. The mirror neuron system (MNS) is a multimodal system composed of neuronal populations that respond to motor, visual, and auditory stimulation, such as when an action is performed, observed, heard, or read about. In humans, the MNS has been identified using neuroimaging techniques. It reflected the integration of motor-auditory-visual information processing related to aspects of language learning, including action understanding and recognition [32]. Based on MNS, embodied cognition theory believes that various cognitive processes (such as concepts, categories, language, reasoning, and judgment) are closely related to the body’s sensorimotor system [33, 34]. Therefore, the realization of language processing should take advantage of the brain motor network, that is, the interweaving and coupling of language processing and motor execution [35]. These theories can demonstrate our findings from the aspect of neural mechanisms.
Our study has some limitations. We did not classify patients according to recovery stage, severity, and the specific brain damage area in patients. Moreover, our study was performed in the cross-section without longitudinal follow-up; thus, whether the recovery stage affects their correlations is unclear. Furthermore, given the proximity of hand-arm and speech-language neural structures, in many patients with poststroke aphasia, the contralesional UE is often simultaneously impaired so that the association between them seems inevitable [9]. However, we know that the Broca area (BA44,45) is adjacent to the UE motor cortex, which is mainly responsible for spontaneous speech ability. Nevertheless, in addition to spontaneous speech, naming, repetition, and comprehension are also positively associated with UE motor conditions, and there should be a deeper neural mechanism worth exploring. Another limitation is that although our study has a large sample size, this also led to a less strict implementation of our inclusion and exclusion criteria, where some of the patients may have been accompanied by other symptoms after stroke. In addition, the fact that the patients were not specifically restricted in terms of damaged brain location and only excluded some patients with large brain lesion only, also diminished the persuasiveness of our findings, and we will go on to restrict these factors in our next study and try to get more rigorous conclusions.
5. Conclusion
To our knowledge, this is the first cross-sectional study to explore the relationship between UE motor status and language function after stroke. Our study demonstrated that patients with PSA tend to be with poorer UE motor status compared to those without PSA, and UE motor status is positively correlated with language function, especially for spontaneous speech ability. Future study should focus more on the deeper mechanisms of the link between UE motor status and language function after strictly controlling the location and severity of brain lesion. In addition, this study provides a new perspective and statistical evidence for a “combined assessment and therapy” approach to UE motor and speech-language rehabilitation, which remains to be demonstrated in future studies.
Authors’ Contributions
Shuo Xu and Zhijie Yan contributed equally to this work and are first authors.
Glossary
Abbreviations
UE:Upper extremity
PSA:Poststroke aphasia
FMA-UE:Fugl-Meyer assessment for the upper extremity
ARAT:Action research and action test
WAB-AQ:Western Aphasia Battery-Aphasia Quotient
BDAE:Boston Diagnostic Aphasia Examination.
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Abstract
Background and Purpose. Poststroke aphasia (PSA) often coexists with upper extremity (UE) motor dysfunction. However, whether the presence of PSA affects UE motor performance, and if language function associates with UE motor performance, are unclear. This study is aimed at (1) comparing the motor status of UE between patients with PSA and without PSA and (2) investigating the association between language function and UE motor status in patients with PSA. Methods. Patients with stroke were compared and correlated from overall and three periods (1-3 months, 4-6 months, and >6 months). Fugl-Meyer assessment for the upper extremity (FMA-UE) and action research and arm test (ARAT) were used to compare the UE motor status between patients with PSA and without PSA through a cross-sectional study among 435 patients. Then, the correlations between the evaluation scale scores of UE motor status and language function of patients with PSA were analyzed in various dimensions, and the language subfunction most closely related to UE motor function was analyzed by multiple linear regression analysis. Results. We found that the scores of FMA-UE and ARAT in patients with PSA were 14 points ((CI) 10 to 18,
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Details



1 Department of Rehabilitation Medicine, Huashan Hospital, Fudan University, Shanghai, China
2 Department of Rehabilitation Medicine, Huashan Hospital, Fudan University, Shanghai, China; Xinxiang Medical University, Xinxiang, China
3 Department of Rehabilitation Medicine, Shanghai Fourth Rehabilitation Hospital, Shanghai, China
4 Department of Neurorehabilitation, The Shanghai Third Rehabilitation Hospital, Shanghai, China
5 Department of Rehabilitation Medicine, Shaanxi Provincial Rehabilitation Hospital, Shaanxi, China
6 Department of Rehabilitation Medicine, Liuzhou Traditional Chinese Medicine Hospital, Guangxi, China
7 Department of Rehabilitation Medicine, The Third Affiliated Clinical Hospital of Changchun University of Chinese Medicine, Jilin, China
8 Department of Rehabilitation Medicine, Nanshi Hospital Affiliated to Henan University, Henan, China
9 Department of Rehabilitation Medicine, Changzhou Dean Hospital, Jiangsu, China
10 Department of Rehabilitation Medicine, Huashan Hospital, Fudan University, Shanghai, China; Shanghai University of Sport, Shanghai, China
11 Department of Rehabilitation Medicine, Huashan Hospital, Fudan University, Shanghai, China; Fujian University of Traditional Chinese Medicine, Fujian, China
12 Department of Rehabilitation Medicine, Huashan Hospital, Fudan University, Shanghai, China; National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, China; National Center for Neurological Disorders, Shanghai, China