Dj. Terris et al., Brain-derived neurotrophic factor-enriched collagen tubule as a substitutefor autologous nerve grafts, ARCH OTOLAR, 127(3), 2001, pp. 294-298
Background: Autologous nerve interposition grafts are frequently harvested
by head and neck sure;eons. The sacrifice of these donor nerves guarantees
sc,me degree of morbidity, including sensory loss, additional incision site
s with associated potential complications, and prolonged operative time. An
alternative to autologous nerve grafting is,: therefore, desirable.
Objective: To determine ifa collagen tubule (CT) filled with either a plain
collagen gel or a brain-derived neurotrophic factor (BDNF)-enriched collag
en gel could be used to achieve functional and histologic outcomes equivale
nt to an autologous nerve graft in bridging a 15-mm nerve gap in the rabbit
facial nerve.
Design: A prospective, randomized, blinded animal study with a control grou
p.
Methods: Thirty rabbit facial nerves were resected (15-mm segments) to crea
te nerve gaps. The gaps were bridged using 1 of 3 methods, assigned randoml
y: a reversed facial nerve (control), a collagen gel-filled CT, or a BDNF-e
nriched collagen gel-filled CT. The animals were evaluated after 6 weeks in
a blinded fashion for functional nerve recovery, axon count, and axonal di
ameter.
Results: There were no significant differences between the autologous nerve
graft group, the collagen gel-filled CT group, or the BDNF-enriched collag
en gel-filled CT group (n=10 for each group) for functional nerve recovery
(P=.94). The mean axon count and the mean axonal diameter were highest in t
he BDNF-enriched collagen gel-filled CT group, but these differences failed
to reach statistical significance (P=.18 and.96, respectively).
Conclusions: Collagen tubules filled with BDNF-enriched collagen gel appear
to be at least as good as autologous nerve grafts for bridging short facia
l nerve gaps. Larger experimental studies are warranted to determine if cli
nical trials are justified.