Published online Jun 26, 2022. doi: 10.4252/wjsc.v14.i6.420
Peer-review started: February 16, 2022
First decision: April 19, 2022
Revised: April 21, 2022
Accepted: June 18, 2022
Article in press: June 18, 2022
Published online: June 26, 2022
Processing time: 127 Days and 22.6 Hours
Treatments involving stem cell (SC) usage represent novel and potentially interesting alternatives in facial nerve reanimation. Current literature includes the use of SC in animal model studies to promote graft survival by enhancing nerve fiber growth, spreading, myelinization, in addition to limiting fibrotic degeneration after surgery. However, the effectiveness of the clinical use of SC in facial nerve reanimation has not been clarified yet.
To investigate the histological, neurophysiological, and functional outcomes in facial reanimation using SC, compared to autograft.
The objectives of our systematic review of the literature and meta-analysis of the comparative studies available in current literature was to investigate the histological, neurophysiological, and functional outcomes in facial reanimation using SC, compared to autograft.
Our study is a systematic review of the literature, consistently conducted according to the preferred reporting items for systematic reviews and meta-analyses statement guidelines. The review question was: In facial nerve reanimation on rats, has the use of stem cells revealed as effective when compared to autograft, in terms of histological, neurophysiological, and functional outcomes? Random-effect meta-analysis was conducted on histological and neurophysiological data from the included comparative studies.
After screening 148 manuscript, five papers were included in our study. 43 subjects were included in the SC group, while 40 in the autograft group. The meta-analysis showed no significative differences between the two groups in terms of myelin thickness [CI: -0.10 (-0.20, 0.00); I2 = 29%; P = 0.06], nerve fibers diameter [CI: 0.72 (-0.93, 3.36); I2 = 72%; P = 0.6], Compound Muscle Action Potential amplitude [CI: 1.59 (0.59, 3.77); I2 = 89%; P = 0.15] and latency [CI: 0.66 (-1.01, 2.32); I2 = 67%; P = 0.44]. The mean axonal diameter was higher in the autograft group [CI: 0.94 (0.60, 1.27); I2 = 0%; P ≤ 0.001].
The role of stem cells in facial reanimation is still relatively poorly studied, in animal models, and available results should not discourage their use in future studies on human subjects.
The role of stem cells in facial reanimation is still relatively new and poorly studied due to the liming nature and number of studies carried out exclusively in animal models. Future studies based on longer follow-up with homogenous criteria, preferably on human subjects, can pave the way to stem cell therapy in patients with nerve palsy.