Increased Incidence of a Midline Brain Anomaly in Patients With Nonsyndromic Clefts of the Lip and/or Palate
Corresponding Author
Peg Nopoulos MD
Department of Psychiatry, University of Iowa College of Medicine, Iowa City.
Dr Nopoulos, University of Iowa College of Medicine, Psychiatry Research, 1-180 MEB, 500 Newton Road, Iowa City, IA 52242. E-mail: [email protected].Search for more papers by this authorStephanie Berg BS
Department of Psychiatry, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorDuane VanDemark PhD
Department of Otolaryngology, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorLynn Richman PhD
Department of Pediatrics, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorJohn Canady MD
Department of Otolaryngology, University of Iowa College of Medicine, Iowa City.
Department of Surgery, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorNancy C. Andreasen MD, PhD
Department of Psychiatry, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorCorresponding Author
Peg Nopoulos MD
Department of Psychiatry, University of Iowa College of Medicine, Iowa City.
Dr Nopoulos, University of Iowa College of Medicine, Psychiatry Research, 1-180 MEB, 500 Newton Road, Iowa City, IA 52242. E-mail: [email protected].Search for more papers by this authorStephanie Berg BS
Department of Psychiatry, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorDuane VanDemark PhD
Department of Otolaryngology, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorLynn Richman PhD
Department of Pediatrics, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorJohn Canady MD
Department of Otolaryngology, University of Iowa College of Medicine, Iowa City.
Department of Surgery, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorNancy C. Andreasen MD, PhD
Department of Psychiatry, University of Iowa College of Medicine, Iowa City.
Search for more papers by this authorABSTRACT
Background and Purpose. Nonsyndromic clefts of the lip and palate (CLP) are developmental craniofacial abnormalities that are often associated with cognitive dysfunction. This study was designed to evaluate, in patients with CLP, the presence of a specific midline brain anomaly (enlarged cavum septi pellucidi [CSP]) that has been shown in other developmental syndromes to be related to poor cognitive function. Methods. Brain images were obtained using magnetic resonance imaging on 49 adult men with CLP and 75 healthy controls. Size of CSP was measured using consecutive coronal images. Results. The incidence of large CSP in the CLP group was 8% (4 of 49), significantly higher than that found in the control group. In 2 of these 4 subjects, the anomaly was complete nonfusion of the septal leaflets, known as a combined CSP and cavum vergae. Furthermore, there was a significant inverse relationship of IQ and CSP in CLP patients that was not present in controls. That is, in individuals with CLP, the larger the CSP, the lower the IQ. Conclusions. Adult men with CLP have an increased prevalence of enlarged CSP. Moreover, this anomaly is directly related to cognitive deficits. This study provides further evidence that the development of the face and the development of the brain are intimately related and that defects in craniofacial development are most likely associated with defects in brain development.
References
- 1 Sarwar M. The septum pellucidum: normal and abnormal. Am J Neuroradiol 1989; 10: 989–1005.
- 2 Nopoulos P, Swayze V, Flaum M, Ehrhardt J, Yuh WTC, Andreasen NC. Cavum septi pellucidi in normals and patients with schizophrenia as detected by MRI. Biol Psychiatry 1997; 41: 1102–1108.
- 3
Johnson V,
Swayze V,
Sato Y,
Andreasen N.
Fetal alcohol syndrome: craniofacial and central nervous system manifestations.
Am J Med Genetics
1996; 61: 329–339.
10.1002/(SICI)1096-8628(19960202)61:4<329::AID-AJMG6>3.0.CO;2-P CAS PubMed Web of Science® Google Scholar
- 4 Renier D, Arnaud E, Cinalli G, Sebag G, Zerah M, Marchac D. Prognosis for mental function in Apert's syndrome. J Neurosurg 1996; 85: 66–72.
- 5 Nopoulos P, Swayze V, Andreasen NC. Pattern of brain morphology in patients with schizophrenia and large cavum septi pellucidi. J Neuropsychiatry Clin Neurosci 1996; 8: 147–152.
- 6 Nopoulos P, Giedd J, Andreasen N, Rapoport J. Frequency and severity of enlarged cavum septi pellucidi in childhood-onset schizophrenia. Am J Psychiatry 1998; 155: 1074–1079.
- 7
Breeding L,
Cowan L,
Bodensteiner J,
Higgans W.
A magnetic resonance imaging study of prevalence and clinical associations in a pediatric population.
J Neuroimaging
1991; 1: 115–118.
10.1111/jon199113115 Google Scholar
- 8 Bodensteiner J, Schaefer G. Wide cavum septum pellucidum: a marker of disturbed brain development. Pediatr Neurol 1990; 6: 391–394.
- 9 Bodensteiner JG, Schaefer GB, Craft JM. Cavum septi pellucidi and cavum vergae in normal and developmentally delayed populations. J Child Neurol 1998; 13: 120–121.
- 10 Schaefer G, Bodensteiner J, Thompson J. Subtle anomalies of the septum pellucidum and neurodevelopmental deficits. Dev Med Child Neurol 1994; 36: 554–559.
- 11 Nopoulos P, Krie A, Andreasen NC. Enlarged cavum septi pellucidi in patients with schizophrenia: clinical and cognitive correlates. J Neuropsychiatry Clin Neurosci 2000; 12: 344–349.
- 12 Goodstein L. Intellectual impairment in children with cleft palates. J Speech Hear Res 1961; 4: 287–294.
- 13 Eliason M. Neuropsychological perspectives of cleft lip and palate. In: J Bardach, H Morris eds. Multidisciplinary Management of Cleft Lip and Palate. Philadelphia , PA : WB Saunders Company; 1990: 825–831.
- 14 Richman LC, Eliason M. Disorders of communication, developmental language disorders and cleft palate. In: CE Walker, MC Roberts eds. Handbook of Child Clinical Psychology-Revised. New York , NY : John Wiley & Sons; 1993.
- 15 Richman LC. Cognitive patterns and learning disabilities in cleft palate children with verbal deficits. J Speech Hear Res 1980; 23: 447–456.
- 16 Kommers M, Sullivan M. Written language skills of children with cleft palate. Cleft Palate J 1979; 16: 81–85.
- 17 Richman LC, Eliason MJ, Lindgren SD. Reading disability in children with cleft lip and/or palate. Cleft Palate J 1988; 25: 21–25.
- 18 Schutte BC, Bjork BC, Coppage KB, et al. A preliminary gene map for the Van der Woude syndrome critical region derived from 900 kb of genomic sequence at 1q32-q41. Genome Res 2000; 10: 81–94.
- 19 Wong FK, Karsten A, Larson O, et al. Clinical and genetic studies of Van der Woude syndrome in Sweden. Acta Odontologica Scandinavica 1999; 57: 72–76.
- 20 Wechsler D. Wechsler Adult Intelligence Scale-Revised, Manual. Cleveland , OH : The Psychological Corporation; 1981.
- 21 Nopoulos P, Berg S, VanDemark D, Richman L, Canady J, Andreasen NC. Cognitive dysfunction in adult males with non-syndromic clefts of the lip and/or palate. Neuro-psychologica (submitted for publication).
- 22 Harris G, Andreasen NC, Cizadlo T, et al. Improving tissue segmentation in MRI: a three-dimensional multispectral discriminant analysis method with automated training class selection. J Comput Assisted Tomogr 1999; 23: 144–154.
- 23 Magnotta VA, Andreasen NC, Schultz SK, et al. Quantitative in vivo measurement of gyrification in the human brain: changes associated with aging. Cereb Cortex 1999; 9: 151–160.
- 24 Shaw CM, Alvord EC. Cava septi pellucidi et vergae: their normal and pathological states. Brain 1969; 92: 213–224.
- 25 Lindgren S, DeRenzi E, Richman L. Cross national comparisons of developmental dyslexia in Italy and the United States. Child Dev 1985; 56: 1404–1417.
- 26
Schaefer GB,
Bodensteiner JB,
Buehler BA,
Lin A,
Cole TRP.
The neuroimaging features of Soto's syndrome.
Am J Med Genetics
1997; 68: 462–465.
10.1002/(SICI)1096-8628(19970211)68:4<462::AID-AJMG18>3.0.CO;2-Q CAS PubMed Web of Science® Google Scholar
- 27 Kwon JS, Shenton ME, Hirayasu Y, et al. MRI study of cavum septi pellucidi in schizophrenia, affective disorder, and schizotypal personality disorder. Am J Psychiatry 1998; 155: 509–515.
- 28 Kjaer I. Human prenatal craniofacial development related to brain development under normal and pathologic conditions [review]. Acta Odontologica Scandinavica 1995; 53: 135–143.
- 29 Sperber G. First year of life: prenatal craniofacial development. Cleft Palate-Craniofac J 1992; 29: 109–111.
- 30 Nopoulos P, Berg S, Canady J, Richman L, VanDemark D, Andreasen NC. Abnormal brain morphology in adult males with isolated clefts of the lip and/or palate: a preliminary analysis. Cleft Palate-Craniofac J 2000; 37: 441–446.
- 31 Wey PD, Neidich JA, Hoffman LA, LaTrenta GS. Midline defects of the orofaciodigital syndrome type VI (Varadi syndrome). Cleft Palate-Craniofac J 1994; 31: 397–400.
- 32 Schrander J, Schrander-Stumpel C, Berg J, Frias JL. Opitz BBBG syndrome: new family with late-onset, serious complications. Clin Genetics 1995; 48(2): 76–79.
- 33 Mitnick R, Bello J, Shprintzen R. Brain anomalies in velocardio-facial syndrome. Am J Med Genetics 1994; 54: 100–106.
- 34 Tsukamoto H, Sakai N, Taniike M, et al. Case of ring chromosome 7: the first report of neuropathological findings. Am J Med Genetics 1993; 46: 632–635.
- 35 Lewis R. A survey of the intelligence of cleft palate children in Ontario. Cleft Palate Bull 1961; 11: 83–85.
- 36 Munson S, May A. Are cleft palate persons of subnormal intelligence Educ Res J 1955; 48: 617–622.
- 37 Ceponiene R, Hukki J, Cheour M, Haapanen ML, Ranta R, Naatanen R. Cortical auditory dysfunction in children with oral clefts: relation with cleft type. Clin Neurophysiol 1999; 110: 1921–1926.