Improvement of language function after Contralateral Seventh Cervical Nerve Transfer in hemiplegic patients combined with post-stroke aphasia: a prospective observational cohort study

Abstract

Background While the contralateral seventh cervical nerve (CC7) cross transfer was designed to reconstruct paralyzed arm function after stroke, improvement in language function was found in patients combined with aphasia. Objective To evaluate the effect of improvement in language function after CC7 cross transfer in stroke patients with chronic aphasia and explore its potential mechanism. Methods In a prospective observative cohort, patients diagnosed with hemiplegia combined with aphasia were included. The language function was evaluated through the changes of Aphasia Quotient evaluated by Western Aphasia Battery (WAB-AQ) as well as its four subtests from baseline to 1 week and 6 months after the surgery. Patients also received oral agility test by Boston Diagnostic Aphasia Examination (BDAE-OA). Resting-state functional MRI (rs-fMRI) was scanned before and over 6 months after the surgery to explore the potential central mechanism in language improvements. Results The average increase of WAB-AQ was 8.08 points from baseline to 1 week post-operatively (P<0.001, 95%CI: 5.05-11.10), and 9.51 from baseline to 6-month (P<0.001, 95%CI: 6.75-12.27). In 8 patients who participant in BDAE-OA, the average increase was 3.7 points (95%CI: 0.56-6.84; corrected P =0.023) from baseline to 1-week follow-up, and 5.3 points from baseline to 6 months follow-up. Significant higher local activity was detected at right precentral cortex, right gyrus rectus, and right anterior cingulate cortex after the surgery from rs-fMRI. Conclusions Immediate and stable improvement in language function was detected after CC7 cross transfer in hemiplegic patients combined with aphasia, which may be realized through enhanced function of language network in the right hemisphere.

Competing Interest Statement

The authors have declared no competing interest.

Clinical Trial

ChiCTR2200060235

Funding Statement

This study was funded by the National Natural Science Foundation of China (82021002, 81830063 and 82072539), CAMS Innovation Fund for Medical Sciences (2019-I2M-5-007), Shanghai Clinical Research Center for Aging and Medicine (19MC1910500), National key R&D program of China (2022YFC3602701), Youth Talent Project of Shanghai Municipal Health Commission (2022YQ009).

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The details of the IRB/oversight body that provided approval or exemption for the research described are given below:

Institutional review board of Shanghai Jing An District Central Hospital gave ethical approval for this work.

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Data Availability

All data produced in the present study are available upon reasonable request to the authors.

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