Purpose: Basic fibroblast growth factor is a mediator of tissue respon
se to injury. Voiding pathology often results in bladder abnormalities
. We prospectively determined whether basic fibroblast growth factor i
s elevated in the urine of children with bladder dysfunction compared
to that of normal controls. Materials and Methods: A total of 97 conse
cutive children with myelomeningocele and 32 with voiding pathology du
e to other etiologies underwent urodynamic testing, and 11 children wi
th no bladder symptoms and sterile urine served as controls. Urinary b
asic fibroblast growth factor levels were assayed by enzyme-linked imm
unosorbent assay and normalized to urinary creatinine. Results: Mean u
rinary basic fibroblast growth factor was higher in bladder dysfunctio
n from myelomeningocele (6,673 pg./gm. creatinine, p = 0.0015) and oth
er etiologies (5,665 pg./gm. creatinine, p = 0.0025) compared with uri
ne from normal bladders (2,995 pg./gm. creatinine). In the myelomening
ocele group urinary tract infection was associated with higher urinary
basic fibroblast growth factor than in sterile urine (9,214 versus 5,
642 pg./gm. creatinine, p = 0.018). Patient age, gender, remote bladde
r surgery, clean intermittent catheterization, detrusor hyperreflexia,
detrusor compliance, age adjusted pressure specific bladder volume, l
ow grade reflux and degree of trabeculation did not correlate with lev
els of basic fibroblast growth factor (p >0.05). Conclusions: Urinary
elevation of basic fibroblast growth factor, a critical mediator of wo
und repair, in children with voiding pathology and clinically abnormal
bladders supports the paradigm that bladder dysfunction may result fr
om generalized response-to-injury mechanisms. The role of fibrogenic c
ytokines, such as basic fibroblast growth factor, merits further direc
ted investigation in bladder pathology.