Genotype-phenotype correlation in 22q11.2 deletion syndrome

The study included 142 individuals referred to the Behavioral Neurogenetics Center (BNC) at Schneider Children’s Medical Center, Petah-Tikva, Israel between January 2001 and December 2009. Mean age 16.1±9.7 years; 78 males (55%) and 64 (45%) females. Sources of referral were: (1) Individuals with FISH confirmed diagnosis of 22q11.2DS referred by clinical genetics departments in Israel; (2) Individuals clinically suspected of the presence of 22q11.2DS, referred by cardiologists, developmental pediatrics, psychiatrists and clinicians at a cleft palate unit.

The study protocol was approved by the Rabin Medical Center Review Board, Petah-Tikva, Israel and written informed consent was obtained from the study participants and their parents or guardians.

Study subjects and their parents underwent a comprehensive medical and developmental intake with a structured clinical checklist composed of the comprehensive multisystem possible clinical symptoms of 22q11.2DS and developmental history [2]. Subjects were referred to further medical evaluations that included cardiac check-up (including electrocardiography and echocardiography), assessment for the presence of typical facial features, evaluation of cleft anomalies (including multi-video fluoroscopy and video endoscopy) and blood calcium levels as previously described [13].

All subjects and their parents were interviewed by skilled clinicians, who were trained until they achieved satisfactory inter-rater reliability scores with the senior investigator (D.G.), using the Hebrew version of the Schedule for Affective Disorders and Schizophrenia for School-Aged Children, Present and Lifetime (K-SADS-PL) [14, 15]. Adults and their parents (when available) were interviewed with the Structured Clinical Interview for Axis I DSM-IV Disorders (SCID) [16]. The ADHD module from the K-SADS was added to the SCID to evaluate the presence of ADHD.

Cognitive evaluation was conducted with the age-appropriate versions of the Wechsler Intelligence Scale [17, 18].

FISH analysis for 22q11.2 deletion was performed according to standard procedures in the cytogenetic laboratory at the Raphael Recanati Genetics Institute, Rabin Medical Center, Israel, using the LSI TUPLE1 (HIRA) or N25 commercial probes (22q11.2) and the LSI ARSA as a sub-telomeric 22q13.3 control probe (Vysis Inc., Downers Grove, IL, USA).

DNA from venous blood was extracted using a commercial kit (Promega Corporation, Madison, WI, USA). All DNA samples were quantified by NanoDrop ND 1000 Spectrophotometer (NanoDrop Technologies, City, USA) and stored at −70°C.

MLPA is a PCR- based method designed to detect gene dosage abnormality by relative quantifications. The SALSA MLPA P250-A1 DiGeorge kit (MRC-Holland, Amsterdam, Netherlands) was used to identify copy number variations (CNVs) in the 22q11.2 region (30 probes) and in other chromosomal regions (4q35, 8p23, 9q34, 10p15, 17p13; 18 probes) according to manufacturer's instructions (http://​www.​mrc-holland.​com). PCR amplification products were separated by capillary electrophoresis using ABI-Prism 3100 Genetic Analyzer (Applied Biosystems, Foster City, CA) at the Hy Laboratories Ltd., Rehovot, Israel. The data were analyzed using the Coffalyser VBA analysis software V8 (http://​www.​mlpa.​com/​coffalyser).

Patients were tested for a deletion in 22q11.2 by the FISH technique as part of their routine workup upon admission to the BNC in order to establish the diagnosis of 22q11.2DS. The 22q11.2 deletion was detected in 109 of 140 subjects (77.8%) using either TUPLE1 (HIRA) or N25 commercial probes. The MLPA test was performed on all patients admitted to the BNC with suspected diagnosis of 22q11.2DS, irrespective of their FISH status, as a confirmatory test to FISH and as a tool for determining the deletion location and boundaries. Using the MLPA P250-A1 DiGeorge kit, a 22q11.2 deletion was detected in 110 (77.5%) of the 142 individuals examined. Duplications were not detected in any of the subjects. Additional probes outside 22q11.2 contained in this kit (from chromosomes 4q34, 8p23, 9q34.3, 10p15, 17p13.3 and 22q13) did not reveal additional CNVs (either deletions or duplications), using a criterion of 'more than one consecutive probe showing significant deviation from the normal values'. A detailed graphical representation of the MLPA analysis for 110 individuals with deletions is depicted in Figure 1. Most subjects (97/110; 88.2%) showed a similar pattern of deletion spanning molecular probes from CLTCL1 to LZTR1 representing the 3Mb TDR.

The deletions in 13 individuals (11.8%) differed from TDR and thus were referred to as non-TDR deletions. Four subjects had a 1.5Mb deletion located between CLTCL1 and DGCR8 probes (LCR A-B), four other subjects had a deletion between CLTCL1 and PCQAP (LCR A-C) and a larger deletion extending from CLTCL1 to HIC2 (LCR A-D+) was identified in 4 individuals (Figure 2). One individual (VC901) carried a short (~1Mb) deletion between LCR B and D+.

There was high agreement between the FISH and MLPA results. All patients identified by FISH (N=109) were confirmed by MLPA, but MLPA identified an additional individual with a 22q11.2 deletion (VC901, Figure 1, 2). This deletion could not be identified by FISH since its starting point is distal to the FISH N25 and TUPLE1 probes (Figure 2). All individuals that were found to be non-deleted by MLPA (N=30) were also FISH negative.

Since the P-250 MLPA kit lacks sufficient probes in the proximal end of the deletion we used the RT qPCR technique as a supplementary method. We studied the deletion status in the proximal breakpoint using SYBR Green labeled PRODH probe and the VPREB1 probe as a control [11]. It was found that the PRODH gene was hemizygously deleted in most (68/71; 95.8%) subjects tested. Out of 3 deletions that did not contain the PRODH gene two were LCR A-D (~3Mb) and one was LCR A-B (1.5Mb).

Tables 1 and 2 summarize the cumulative physical and psychiatric data of the 110 subjects with 22q11.2 deletions grouped according to the type of deletion. There are 97 individuals with TDR and 13 individuals divided into four groups of different types of non-TDR deletions. The small number of individuals in each of the different non-TDR deletions and the inherent variability of the clinical data preclude rigorous statistical analysis. However, it can be seen that there are no large differences between the groups in terms of physical and psychiatric manifestations typical to the 22q11.2DS. It is of note that hypocalcemia was present in 27.7% (28/101) of individuals with 3Mb and larger deletions and in none (0/8) of the individuals with the smaller proximal deletions (1.5 and 2Mb) (Table 1).

Table 3 gives a detailed description of the clinical data of each the 13 non-TDR subjects. Individuals with the 1.5Mb deletion (LCR A-B) exhibited fewer cardiovascular anomalies compared to the other non-TDR subjects (1/4, 25% vs. 8/9, 88.9%; p=0.052).

Patient VC901 carried a distal LCR B-D+ deletion located between ZNF74 and HIC2 probes (Figure 2). We elaborate below on the clinical features of this patient because she carried a rare deletion with only two other similar cases in the literature [19, 20] and may allow studying the impact of the deleted genes in this patient on its particular phenotype. Patient VC901 was referred to our clinic at the age of 10 years as a suspected 22q11.2DS by a trained speech therapist based on her physical and neuropsychiatric profile. FISH analysis using the N25 probe failed to detect a deletion in this individual. Patient VC901 was born with ventricular septal defect (VSD) that was corrected by surgery, cleft lip and palate, retrognathia, hypernasal speech, and short stature (below the third percentile for height, weight and head circumference). The facial features share some similarities with 22q11.2DS (see Figure 3). She has a broad square face, hypotelorism, narrow nasal base and broad nasal bridge, overhanging nasal tip, deviated nasal tip (state post cleft lip repair), short philtrum, narrow mouth, chin dimple and broad neck. Already at the age of 5 years she was diagnosed with dysgraphia and dyscalculia. Results on Wechsler testing at the age of 10 years were: full scale IQ 59 (verbal IQ 69, performance IQ 55). Psychiatric assessment at the age 13 years conducted by K-SADS indicated that Patient VC901 is suffering from severe anxiety disorders including generalized and separation anxiety disorders and specific and social phobias. In addition Patient VC901 was coping with ADHD, predominantly inattentive type. She also exhibited bizarre behaviors which were diagnosed as subthreshold psychotic symptoms. On second evaluation at the age of 20 years Patient VC901 was diagnosed with psychotic disorder not otherwise specified, marked by delusions of reference and recurrent episodes in which she threatened to stab her parents with a knife, with a Positive and Negative Syndrome Scale (PANSS) score of 89. Her cognitive performance showed some improvement compared to the first evaluation with full scale IQ score 67 (verbal IQ 73, performance IQ 65).

In 32 (22.5%) of 142 subjects referred to the BNC with suspicion of 22q11.2DS no deletions were detected either by MLPA or by FISH. To illustrate the problematic diagnosis of subjects showing some 22q11.2DS-like phenotype but with no apparent deletion we selected 12 individuals with the most pronounced clinical manifestations typical to 22q11.2DS and present them in Table 4.

Interestingly, it appears that the variety and severity of the clinical symptoms in these subjects are very similar to those found in confirmed 22q11.2DS patients.

We identified 5 types of 22q11.2 deletions. According to the results of the specific MLPA kit used, the proximal starting point for all deletions, except one, was located in the CLTCL1 gene probe, near LCR A (Figure 2). The distal breakpoints of the deletions were located in LCRs B, C, D and D+ thus determining the size and location of the deletions. Ninety seven out of 110 individuals (88.2%) carried the typical ~3Mb deletion (LCR A-D) consistent with frequencies found in other studies (77–88.7%) [20, 21, 24‐27].

The largest deletion (LCR A-D+), a variant of the 3Mb deletions, was present in 3.63% of the subjects compared to 4.5-6.5% in previous reports [8, 24]. The prevalence of the proximal deletions of 1.5Mb (LCR A-B) and 2Mb (LCR A-C), each 3.63% in our subjects, varied largely in other studies [20, 21, 24‐27], probably due to different sample sizes and resolution of the mapping methods used.

Studying the genotype-phenotype relationship in 22q11.2DS is a formidable task. The difficulties are obvious: there are up to 200 possible clinical symptoms [4], the clinical variability is large even in individuals with the same type of deletion and the statistical power is low because most individuals harbor the common 3Mb TDR and only a few with other entities. Yet, it can potentially shed light on the role of the genes that contribute to the physical and psychiatric symptoms expressed in this disorder. The quantitative comparison between 97 individuals with TDR and those with four different types of nonTDR deletions along several physical and neuropsychiatric-cognitive parameters did not reveal statistically significant differences. This could be due to methodological limitations such as sample size, and the complexity of the genetic and epigenetic mechanisms governing the phenotype in 22q11.2DS. Our results are supported by most previous studies that could not demonstrate a correlation between the size and the location of the deletion and the clinical features of the subjects [24, 25, 28‐30]. However, Rauch et al. (2005) demonstrated a correlation between deletion characteristics and phenotypic expression by assessment of individuals with typical and atypical 22q11.2 deletions, showing that atypical CHD and mild dysmorphism are recognizable feature of atypical distal deletions [20]. Recently, a case-report of monozygotic twins differing in their deletion size and clinical expression was published, indicating a possible role of deletion characteristics for the phenotype [31].

In accordance with previous studies [32] hypocalcemia was found in 27.7% of patients with large deletions (3Mb, LCR A-D and LCR A-D+) but was absent in those carrying the proximal nested deletions (1.5 and 2Mb). Interestingly, neither was it observed in patients with distal nested deletions [33]. Although the number of cases is small, this observation may suggest that haploinsufficiency of genes both at the proximal and the distal part of 22q11.2 is required in order to cause hypocalcemia.

The presented clinical data of each individual carrying a non-TDR deletion are not in themselves informative but may be of help in the effort to build a common data base. More informed and educated conclusions could be made on this intriguing question by applying unified molecular methods for mapping the 22q11.2 deletion (high resolution methods such as CGH and SNP arrays and next generation sequencing) and using agreed clinical parameters and scoring system for characterizing the phenotype.

Before the era of molecular diagnosis patients were diagnosed as VCFS (22q11.2DS) solely based on their clinical symptoms. When molecular genetics methods were introduced it turned out that in about 20% of the patients classified as VCFS no deletion could be detected [20, 21] and the question of the etiology of their phenotype is still unknown. Interestingly, when we examined a subgroup of these individuals it appeared that the variety and severity of clinical symptoms in these subjects are very similar to those found in confirmed 22q11.2DS patients. Subjects may have been misdiagnosed because they had a combination of relatively common symptoms, such as cardiac anomalies and neuropsychiatric disorders, that when considered together phenocopy the 22q11.2DS. It is also possible that these patients do carry very small deletions or even point mutations which are below the resolution of the methods used or they have other microdeletion or microduplication syndromes.

Patient VC901 carries a rare, small deletion that does not include the nested proximal 1.5Mb region which harbors several important candidate genes, thought to be sufficient for producing the syndrome [34]. This case portrays the complexity of the molecular mechanisms controlling the 22q11.2DS phenotype, indicating the possibility of redundancy in causative genes. Since the "classical" candidate genes are not deleted in this person other candidate genes residing in the nested distal region may be responsible for the physical features and neuropsychiatric manifestations. For example, of the candidate genes that have been shown to be involved in cardiac malformations (HIRA, UFD1L, TBX1 and CRKL) [35‐39]CRKL is one that is located in the distal deletion region and has been found to affect cardiac neural crest derivatives in mice [36]. Its loss may be the causative event for the CHD in this case. In a similar manner, the neuropsychiatric phenotype may be affected by the deletion of PIK4CA and SNAP29 from the distal region which have been demonstrated to be associated with schizophrenia [40‐43], and not by the putative schizophrenia genes PRODH, COMT, DGCR8 and ZDHHC8. Another genetic mechanism that may affect the phenotype involves control elements in the deleted region that act by cis mechanisms on the expression of the non-deleted candidate genes as in the dosage-sensitive interaction between Tbx1and Crkl in mice [44].

The longitudinal neuropsychiatric follow-up of this patient has raised the intriguing question of whether multiple genes in the 22q11.2 region are responsible for the emergence of schizophrenia in 22q11.2DS patients. Her psychiatric developmental trajectory is typical of 22q11.2DS namely, anxiety and subthreshold positive psychotic symptoms during childhood evolving to a full psychotic disorder in adulthood. Yet her cognitive developmental trajectory is not typical, as her IQ scores did not decline and even improved a little during young adulthood, whereas in typical 22q11.2DS patients there is a cognitive decline especially of verbal IQ [45, 46]. This might suggest that the neuropsychiatric manifestations in 22q11.2DS are governed by several sets of genetic elements. It is tempting to speculate that genes such as PIK4CA and SNAP29 that are deleted in our patient may be involved in the emergence of psychotic "positive symptoms" while others, such as PRODH and COMT that are not deleted, play a role in the cognitive decline process.

Two other 22q11.2DS cases with similar distally nested deletion have been reported but they are not readily comparable to the present case because of the probands' young age. One was a patient with TOF and facial dysmorphology, last assessed at 9 months of age [19], and the other a 6 year-old with typical facial features, significant developmental delay and increased anxiety suggestive of possible early signs of psychiatric illness [20].