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CNV “Double Whammies” May Account for Variable Neuropsychiatric Phenotypes

22 February 2010. Copy number variants (CNVs) have promised to account for some of the heritability for psychiatric diseases not captured in genomewide association studies (GWASs). While there is little question that these genetic deletions and duplications contribute significantly to disease risk, clear mechanistic conclusions have been difficult to draw because several CNVs studied so far are associated with a wide range of phenotypes.

The authors of a new Nature Genetics paper on a 16p12.1 microdeletion associated with developmental delay say their results suggest that some of the striking phenotypic variation seen in previous CNV studies—whether in the form of distinct clinical features or severity of illness—may be explained by a “two-hit” model: a given CNV may predispose individuals for a neuropsychiatric phenotype, and also exacerbate phenotypic expression or introduce distinct clinical features in conjunction with a second CNV.

In a meta-analysis carried out last year (Itsara et al., 2009), members of the team directing the new study—led by Evan Eichler of the University of Washington, with collaborators at the University of California-San Diego, Harvard, and the University of Auckland, among other institutions—identified the 520 kb deletion in question in five individuals affected by autism or schizophrenia, but there was insufficient statistical power to definitively implicate the CNV in those disorders.

To take a closer look at this CNV, co-first authors Santhosh Girirajan of the University of Washington and Jill Rosenfeld of Signature Genomic Laboratories, Spokane, Washington, and their colleagues assembled large discovery and replication cohorts, with a combined total of more than 20,000 cases of intellectual disability or developmental delay and nearly 15,000 controls. They also studied a smaller schizophrenia cohort of about 3,000 patients and compared it to the same 15,000 controls.

In this study, they found that the 16p12.1 CNV was significantly enriched in the cases of developmental delay, being found in 42 cases versus eight controls (P = 1.18 x 10-4). There was no significant association between the CNV and schizophrenia in the smaller cohort, but the authors could not rule out insufficient statistical power underlying this result.

As in previous CNV studies, the cases exhibited a gamut of phenotypes: the most common observations were developmental delay, speech delay, and craniofacial and skeletal anomalies, but medical records also revealed retarded growth, microcephaly, cardiac defects, seizures, psychiatric diagnoses, and more.

An added burden
However, cases were not only more likely to carry the 16p21.1 deletion; they were six times more likely than controls, including controls carrying some >500 kb CNV other than the 16p21.1 deletion, to carry “double hits”: a second CNV >500 kb or some other significant chromosomal abnormality. Compared to the general population, cases were 60-fold more likely to carry these double hits.

Two-hit carriers had more “severe or distinct” phenotypes than those who carried just the 16p21.1 deletion, say the authors. One case carried the 16p21.1 CNV plus a 22q13 terminal deletion that has been associated with Phelan-McDermid syndrome, featuring autism spectrum disorders and macrocephaly (Phelan et al., 2001; Durand et al., 2007). However, this case exhibited microcephaly and no autistic features (at two years, three months of age). Another case carrying a second deletion hit at 5q15q23.2, which has been associated with craniofacial features and benign intestinal polyps (Lindgren et al., 1992), exhibited more severe craniofacial and cognitive phenotypes than had been reported for the 5q15q23.2 deletion alone. A carrier of an 848 kb duplication on 14q32.1, who also carried a mutation in the BRAF gene consistent with a diagnosis of cardiofaciocutaneous syndrome (CFCS), exhibited a “diverse range of severe clinical features including craniofacial anomalies; complete agenesis of the corpus callosum; renal and cardiac defects; and Hirschsprung disease,” a far more severe clinical picture than that so far described for either CFCS or a case of a de novo 14q32.1 reported in association with schizophrenia (Xu et al., 2008).

Revisiting chromosome 1
Members of the research team are no strangers to the phenotypic puzzles posed by CNVs. In 2008, Eichler and coauthor Heather Mefford, both at Washington, led a study of patients with a 1.35 mb deletion or reciprocal duplication in a region of 1q21.1 spanning seven genes (Mefford et al., 2008; also see SRF related news story and Q&A with Eichler and Mefford). Patients in that study carrying the 1q21.1 deletion had mild to moderate developmental delay accompanied by dysmorphic features, and those carrying the duplication exhibited learning disabilities, mental retardation, or autism. However, a broad spectrum of other phenotypes—skeletal, facial, cardiac, ocular, neurological—that displayed no syndromic pattern led the authors to conclude that the observations “dispel the notion that rare copy-number variants will necessarily follow the one gene- (or one rearrangement-) one disease model.”

In light of the high incidence of two genetic hits in the 16p21.1 carriers in the current study, the researchers re-examined 25 cases carrying the 1q21.1 deletion, and found a 40-fold enrichment for a second large CNV in that group. Again the phenotypes were highly variable, “ranging from severe neurological deficit and craniofacial abnormalities to severe schizophrenia without cognitive impairment.”

An additional analysis of eight other syndromic and non-syndromic genomic disorders revealed that carriers of the 16p21.1 deletion ranked highest for second hits, followed closely by other CNVs for which variable phenotypes have been reported (e.g., 15q13.3, 16p11.2, and 22q11.2). The researchers found an inverse correlation between de novo CNVs and a second, with 16p12.1 as a case in point. Only a single de novo 16p12.1 deletion has been reported, but this CNV had the highest likelihood of the presence of a second hit in inherited CNV cases.

Though the current study focuses on double CNV hits, the authors offer a broad definition of their model, in which “[t]he second hit could potentially be another CNV, a disruptive single-base-pair mutation in a phenotypically related gene or an environmental event that influences the phenotype.” Overall, they write, “Our ‘two-hit’ model might...help to explain the significant comorbidity that exists among cognitive impairment, schizophrenia, and autism, and the underlying phenotypic variability reported for several recurrent deletions.”—Pete Farley.

Reference:
Girirajan S, Rosenfeld JA, Cooper GM, Antonacci F, Siswara P, Itsara A, Vives L, Walsh T, McCarthy SE, Baker C, Mefford HC, Kidd JM, Browning SR, Browning BL, Dickel DE, Levy DL, Ballif BC, Platky K, Farber DM, Gowans GC, Wetherbee JJ, Asamoah A, Weaver DD, Mark PR, Dickerson J, Garg BP, Ellingwood SA, Smith R, Banks VC, Smith W, McDonald MT, Hoo JJ, French BN, Hudson C, Johnson JP, Ozmore JR, Moeschler JB, Surti U, Escobar LF, El-Khechen D, Gorski JL, Kussmann J, Salbert B, Lacassie Y, Biser A, McDonald-McGinn DM, Zackai EH, Deardorff MA, Shaikh TH, Haan E, Friend KL, Fichera M, Romano C, Gécz J, DeLisi LE, Sebat J, King MC, Shaffer LG, Eichler EE. A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nat Genet. 2010 Feb 14. Abstract

 
Comments on News and Primary Papers
Comment by:  Ben Pickard
Submitted 25 February 2010 Posted 25 February 2010

In their Nature Genetics paper, Girirajan et al....  Read more


View all comments by Ben Pickard
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