Myelomeningocele sac associated with worse lower-extremity neurological sequelae: evidence for prenatal neural stretch injury?

E R Oliver, G G Heuer, E A Thom, P K Burrows, R A Didier, S E DeBari, J S Martin-Saavedra, J S Moldenhauer, J Jatres, L J Howell, N S Adzick, B G Coleman, E R Oliver, G G Heuer, E A Thom, P K Burrows, R A Didier, S E DeBari, J S Martin-Saavedra, J S Moldenhauer, J Jatres, L J Howell, N S Adzick, B G Coleman

Abstract

Objective: To determine whether the presence of a myelomeningocele (MMC) sac and sac size correlate with compromised lower-extremity function in fetuses with open spinal dysraphism.

Methods: A radiology database search was performed to identify cases of MMC and myeloschisis (MS) diagnosed prenatally in a single center from 2013 to 2017. All cases were evaluated between 18 and 25 weeks. Ultrasound reports were reviewed for talipes and impaired lower-extremity motion. In MMC cases, sac volume was calculated from ultrasound measurements. Magnetic resonance imaging reports were reviewed for hindbrain herniation. The association of presence of a MMC sac and sac size with talipes and impaired lower-extremity motion was assessed. Post-hoc analysis of data from the multicenter Management of Myelomeningocele Study (MOMS) randomized controlled trial was performed to confirm the study findings.

Results: In total, 283 MMC and 121 MS cases were identified. MMC was associated with a lower incidence of hindbrain herniation than was MS (80.9% vs 100%; P < 0.001). Compared with MS cases, MMC cases with hindbrain herniation had a higher rate of talipes (28.4% vs 16.5%, P = 0.02) and of talipes or lower-extremity impairment (34.9% vs 19.0%, P = 0.002). Although there was a higher rate of impaired lower-extremity motion alone in MMC cases with hindbrain herniation than in MS cases, the difference was not statistically significant (6.6% vs 2.5%; P = 0.13). Among MMC cases with hindbrain herniation, mean sac volume was higher in those associated with talipes compared with those without talipes (4.7 ± 4.2 vs 3.0 ± 2.6 mL; P = 0.002). Review of the MOMS data demonstrated similar findings; cases with a sac on baseline imaging had a higher incidence of talipes than did those without a sac (28.2% vs 7.5%; P = 0.007).

Conclusions: In fetuses with open spinal dysraphism, the presence of a MMC sac was associated with fetal talipes, and this effect was correlated with sac size. The presence of a larger sac in fetuses with open spinal dysraphism may result in additional injury through mechanical stretching of the nerves, suggesting another acquired mechanism of injury to the exposed spinal tissue. Copyright © 2019 ISUOG. Published by John Wiley & Sons Ltd.

Keywords: clubfoot deformity; fetal MRI; fetal surgery; myelomeningocele; myeloschisis; obstetrical ultrasound; spina bifida; talipes.

Copyright © 2019 ISUOG. Published by John Wiley & Sons Ltd.

References

REFERENCES

    1. Tortori-Donati P, Rossi A, Cama A. Spinal dysraphism: A review of neuroradiological features with embryological correlations and proposal for a new classification. Neuroradiology 2000; 42: 471-491.
    1. Adzick NS, Sutton LN, Crombleholme TM, Flake AW. Successful fetal surgery for spina bifida. Lancet 1998; 350: 1675-1676.
    1. Bouchard S, Davey MG, Rintoul NE, Walsh DS, Rorke LB, Adzick NS, Farmer D, O'Neill J. Correction of hindbrain herniation and anatomy of the vermis after in utero repair of myelomeningocele in sheep. J Pediatr Surg 2003; 38: 451-458.
    1. Copp AJ, Adzick NS, Chitty LS, Fletcher JM, Holmbeck GN, Shaw GM. Spina bifida. Nat Rev Dis Prim 2015; 1: 1-18.
    1. Coleman BG, Langer JE, Horii SC. The diagnostic features of spina bifida: The role of ultrasound. Fetal Diagn Ther 2015; 37: 179-196.
    1. Bulas D. Fetal evaluation of spine dysraphism. Pediatr Radiol 2010; 40: 1029-1037.
    1. Mirsky DM, Schwartz ES, Zarnow DM. Diagnostic features of myelomeningocele: The role of ultrafast fetal MRI. Fetal Diagn Ther 2015; 37: 219-225.
    1. Servaes S, Hernandez A, Gonzalez L, Victoria T, Johnson M, Jaramillo D, Edgar JC, Johnson A. Fetal MRI of clubfoot associated with myelomeningocele. Pediatr Radiol 2010; 40: 1874-1879.
    1. Farmer DL, Thom EA, Brock JW, Burrows PK, Johnson MP, Howell LJ, Farrell JA, Gupta N, Adzick NS. The Management of Myelomeningocele Study: full cohort 30 month outcomes. Am J Obstet Gynecol 2018; 218: 256.e1-13.
    1. Wilson RD, Johnson MP, Bebbington M, Flake AW, Hedrick HL, Sutton LN, Adzick NS. Does a myelomeningocele sac compared to no sac result in decreased postnatal leg function following maternal fetal surgery for spina bifida aperta? Fetal Diagn Ther 2007; 22: 348-351.
    1. Adzick NS, Thom EA, Spong CY, Brock JW, Burrows PK, Johnson MP, Howell LJ, Farrell JA, Dabrowiak ME, Sutton LN, Gupta N, Tulipan NB, Dalton ME, Farmer DL. A randomized trial of prenatal versus postnatal repair of myelomeningocele. N Engl J Med 2011; 364: 993-1004.
    1. Nagaraj UD, Bierbrauer KS, Stevenson CB, Peiro JL, Lim F-Y, Zhang B, Kline-Fath BM. Myelomeningocele versus myelocele on fetal MR images: are there differences in brain findings? Am J Roentgenol 2018; 211: 1376-1380.
    1. Heffez DS, Aryanpur J, Hutchins GM, Freeman JM. The paralysis associated with myelomeningocele: Clinical and experimental data implicating a preventable spinal cord injury. Neurosurgery 1990; 26: 987-992.
    1. Rethmann C, Scheer I, Meuli M, Mazzone L, Moehrlen U, Kellenberger CJ. Evolution of posterior fossa and brain morphology after in utero repair of open neural tube defects assessed by MRI. Eur Radiol 2017; 27: 4571-4580.

Source: PubMed

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