Research Article | Open Access
Fang Fang, Minxia Ge, Jun Liu, Zengyu Zhang, Hong Yu, Shuilong Zhu, Liwei Xu, Lina Shao, "Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder", Behavioural Neurology, vol. 2021, Article ID 4150926, 6 pages, 2021. https://doi.org/10.1155/2021/4150926
Association between Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and Risk of Childhood Autism Spectrum Disorder
Objective. Genetic factors play an important role in the development of autism spectrum disorder (ASD). This case-control study was to determine the association between childhood ASD and single nucleotide polymorphisms (SNPs) rs3746599 in the DUSP15 gene, rs7794745 in the CNTNAP2 gene, and rs251379 in the PCDHA gene in a Chinese Han population. Methods. Genotypes of SNPs were examined in DNA extracted from blood cells from 201 children with ASD and 200 healthy controls. The Children Autism Rating Scale (CARS) was applied to evaluate the severity of the disease and language impairment. The relationship between SNPs and the risk of ASD or the severity of the disease was determined by logistic regression and one-way ANOVA. Results. The genotype G/G of rs3746599 in the DUSP15 gene was significantly associated with a decreased risk of ASD (odds ratio , 95% confidence interval (CI): 0.42-0.99, ). The T allele of rs7794745 in the CNTNAP2 gene was associated with an increased risk of ASD (, 95% CI: 1.01-1.77, ). The SNP rs251379 was not associated with ASD. Though none of the SNPs examined were associated with ASD severity, rs7794745 was associated with severity of language impairment. Conclusions. Our findings suggest that both rs3746599 in the DUSP15 gene and rs7794745 in the CNTNAP2 gene are associated with risk of childhood ASD, and rs7794745 is also related to the severity of language impairment in autistic children from a Chinese Han population.
Autism spectrum disorder (ASD) is a neurodevelopmental disorder that presents with social and communicative deficits and repetitive behaviors. With increased attention and improved diagnoses, the prevalence of the disease has been increasing in China . The wide prevalence of this disease brings huge economic burdens to families and society. Early diagnosis and intervention are essential to improve the efficacy of treatment. Though the etiology of the disease has not been fully elucidated, genetic factors have been implicated as important risk factors in the pathogenesis of ASD [2, 3]. One of the most common types of genetic variants, single nucleotide polymorphisms (SNPs), in certain genes may impact the susceptibility to ASD. Identification and validation of these ASD-related SNPs will assist in the development of early diagnoses and more efficient treatments.
Dual-specificity phosphatase 15 (DUSP15) is a member of the family of dual-specificity phosphatases possessing the ability to dephosphorylate both phosphoserine/threonine and phosphotyrosine residues. The DUSP15 gene was shown to regulate myelination in oligodendrocytes and their differentiation and development . Myelination control and axon support by oligodendrocytes are essential for the normal functions of complex neural cellular networks . Pathology of oligodendrocytes has been correlated with ASD. Patients with ASD were found to have fewer oligodendrocytes in the amygdala compared to typically developing controls . In addition, the intronic SNP rs3746599 in the DUSP15 gene has been identified as a risk factor for childhood ASD .
The CNTNAP2 gene product is a member of the neurexin superfamily of proteins that are highly expressed throughout the brain and spinal cord and facilitate cell–cell interactions in the nervous system . By interacting with transient axonal protein 1, the CNTNAP2 protein at the juxtaparanodal region stimulates myelinating glial cells to organize ion channels in the underlying axonal membrane . Independent studies have demonstrated a positive correlation between mutations in CNTNAP2 and susceptibility for ASD [10–13]. Transgenic mice lacking Cntnap2 display striking similarity to the core deficits in behavioral and cognitive functions observed in patients with ASD . The intronic SNP rs7794745 in the CNTNAP2 gene was reported to be a risk factor for ASD in some studies [15–17], but not others [18, 19].
The protocadherins (PCDH) are the cadherin superfamily of calcium-dependent cell adhesion molecules which include the nonclustered genes and the α, β, and γ clustered genes [20, 21]. The PCDHα (PCDHA) is composed of 15 large, variable region exons arrayed in tandem and a constant region composed of 3 exons . The PCDHA and other PCDHs mediate homophilic matching between different cell types for the formation and function of complex neural networks . The PCDHA protein is localized at the specific synaptic junctions and thus plays an important role in specific synaptic connections . Impaired neuronal connectivity due to altered synapses has been attributed to cognitive deficits . This protein is also important for appropriate innervation of target brain areas by serotonergic projections . Abnormal serotonin signaling has been associated with the development of ASD [25, 26]. Furthermore, the SNP rs251379, localized in the introns of the PCDHA1-12 genes, has been reported to be correlated with the risk of ASD . Taken together, these findings imply that the PCDHA is a possible susceptibility gene for ASD.
Previous studies suggest that DUSP15, CNTNAP2, and PCDHA are important in maintaining the functional connectome of the brain and optimal information processing in complex neural networks. It is noted that the aforementioned SNPs in these genes have only been individually studied in different populations. Due to the wide ranges of disease presentations caused by varied genetic and environmental factors, findings for ASD-related SNPs need to be corroborated in individual ethnic populations. The objective of this study was to determine the relationship between childhood ASD and the SNPs rs3746599 in DUSP15, rs7794745 in CNTNAP2, and rs251379 in PCDHA in a Chinese Han population. Related SNPs may serve as candidate biomarkers for the diagnosis of ASD in the future studies.
2. Patients and Methods
A total of 201 autistic children and 200 age- and gender- matched healthy children were enrolled in this study from 2012 to 2016 [28–30]. The severity of ASD was evaluated using the Children Autism Rating Scale (CARS). There are 14 domains to evaluate individual behaviors and a 15th domain for general impressions in CARS. Each domain is scored from one to four. A higher score indicates a more severe symptom of the domain. Autistic children with total were classified as mild/moderate, and total were classified as severe. The language communication domain scores in CARS were used to evaluate the severity of language impairment in autistic children. This study was approved by the Medical Ethics Committee of Zhejiang Xiaoshan Hospital. Informed consent was obtained from parents or guardians of all children.
Genotypes were analyzed in DNA extracted from blood cells using a TaqMan probe-based approach. The probes were designed and synthesized by Applied Biosystems (Beijing, China). Real-time PCR was conducted following the manufacturer’s protocol, described previously .
For statistical analysis of all SNP frequencies, the Hardy-Weinberg equilibrium was examined using the test. Logistic regression analysis was applied to examine the association between SNPs and the risk of childhood ASD or severity of the disease. Odds ratios (ORs) and 95% confidence intervals (CIs) were calculated. One-way ANOVA was applied to analyze the difference in language communication domain scores among the SNPs of interest. Group-wise comparisons were made using the Tukey test. Statistical analyses were performed using the SAS 9.3 software (SAS Institute Inc., Cary, NC). A value < 0.05 was considered to be significant.
Genotype distributions of rs3746599 in DUSP15, rs7794745 in CNTNAP2, and rs251379 in PCDHA were all consistent with the Hardy-Weinberg equilibrium in both case and control groups (Table 1).
Results from logistic regression analysis showed that the G/G genotype of rs3746599 in DUSP15 (, 95% confidence interval , ) was significantly associated with decreased risk of childhood ASD. There was no significant difference in allele frequency of rs3746599 in autistic children compared to healthy controls (Table 2). The T/T genotype of rs7794745 in CNTNAP2 was marginally associated with an increased risk of ASD (, , ). The T allele was significantly associated with an increased risk of ASD (, , ) (Table 2). Neither genotype nor allele distributions of rs251379 in PCDHA were significantly associated with risk of childhood ASD (Table 2).
OR: odds ratio; CI: confidence interval.
The relationship between these SNPs and childhood ASD was further analyzed using dominant and recessive models of inheritance for rs3746599 in DUSP15, rs7794745 in CNTNAP2, and rs251379 in PCDHA. No significant association between these SNPs and risk of ASD was observed in any of these models (Table 3).
OR: odds ratio; CI: confidence interval.
Children affected with ASD were classified into mild/moderate and severe groups based on CARS scores. There were 122 children with mild-to-moderate ASD and 79 with severe ASD. Logistic regression analysis showed that there was no significant association between the presence of these SNPs and the severity of childhood ASD (Table 4).
OR: odds ratio; CI: confidence interval.
The association between the SNPs and the severity of language impairment was further examined in autistic children. Our results indicated that the genotype A/A was associated with a significantly lower language communication domain score compared to the T/T or T/A genotypes of rs7794745 in CNTNAP2. There was no significant difference in language communication domain score among genotypes of rs3746599 in DUSP15 or rs251379 in PCDHA (Table 5).
Different letter indicates significant difference among the genotypes of the same SNP group.
ASD is a multifactorial disease caused by both genetic and environmental factors. Our current study determined the association between three SNPs and childhood ASD in a Chinese Han population. The results showed that the SNP rs3746599 in the DUSP15 gene and rs7794745 in the CNTNAP2 gene, but not rs251379 in PCDHA, were risk factors for childhood ASD. Although none of the SNPs were associated with severity of the disease, rs7794745 in CNTNAP2 was significantly associated with severity of language impairment.
As a key regulator for oligodendrocyte differentiation and myelin production, the DUSP15 gene plays an important role in the development and function of the nervous system . The rs3746599 SNP in the DUSP15 gene was predicted to be within the conserved transcription factor binding site and thus influence the binding ability of transcription factors and, consequentially. gene expression . A previous study determined an association between the DUSP15 SNP rs3746599 and childhood ASD in a Chinese Han population. A total of 255 autistic children and 427 healthy controls were enrolled in the case-control study. SNP rs3746599 genotypes were examined by Sanger sequencing. Their results showed that SNP rs3746599 was significantly associated with childhood ASD under allelic, additive, and dominant models . Using the same ethnic population from a different region in China, our data also showed that SNP rs3746599 in DUSP15 was significantly associated with ASD. Taken together, results from both studies indicate that DUSP15 is a susceptibility gene for ASD and that SNP rs3746599 is a potential marker that might be used in screening for ASD in this population.
Several groups have studied the association between rs7794745 in the CNTNAP2 gene and the risk of ASD. An Iranian case-control study analyzed rs7794745 genotypes and frequencies in a total of 200 autistic patients and 260 healthy individuals. The genotype frequencies of AA, AT, and TT were 35.3%, 50.7%, and 13.8% in controls and 32%, 68%, and 0% in autistic patients, respectively. SNP rs7794745 in CNTNAP2 was significantly associated with ASD in this population . A significant association between the T allele of rs7794745 and the increased risk of high functioning ASD was reported in the case-control study from a European group . A Brazilian group examined CNTNAP2 rs7794745 and rs2710102 in 210 patients with ASD and 200 healthy individuals. Their results revealed a significantly higher frequency of the TT allele of rs7794745 in ASD patients compared to controls . Consistent with this finding, this study found a significant association between the T allele of rs7794745 and increased risk of ASD in a Chinese Han population in this study. Another study in the same Chinese Han population showed a significant correlation between ASD and haplotype T-A (rs7794745-rs10500171, ) or haplotype A-T-A (rs10244837-rs7794745-rs10500171) of the CNTNAP2 gene . However, several other studies reported no significant association between rs7794745 and the risk of ASD [18, 19].
The role of the PCDHA SNP rs251379 in the development of ASD was also evaluated in this study. No significant association between rs251379 and ASD was observed. In contrast to this finding, a previous study examined the genetic association of PCDHA with ASD in a cohort of 841 families that included a total of 3211 individuals. Among 14 PCDHA SNPs examined, rs251379 was one of the five SNPs significantly associated with ASD . This result suggests more study is needed to validate rs251379 in the PCDHA gene as a risk factor for ASD in a Chinese population.
Language impairment is a common sign of ASD. The severity of language impairment was based on the scores of the language communication domain in the CARS. This study determined the correlation between three SNPs and severity of language impairment in children with ASD. Our results revealed that only rs7794745, but not rs3746599 or rs251379, was significantly associated with severity of language impairment. Several independent studies reported the effects of the rs7794745 SNP in the CNTNAP2 gene on the brain activities of vocal communication and language processing in healthy individuals [35–38]. Homozygous risk allele of rs7794745 was associated with significant reductions in grey and white matter volume and fractional anisotropy in several regions . All these findings suggest that the impact of rs7794745 on brain structure and brain activities during language processing may contribute to the severity of language impairment observed in this study. More studies are needed to elucidate the mechanisms accounting for the effect of rs7794745 on language impairment in patients with ASD.
Our study finds that the DUSP15 rs3746599 and CNTNAP2 rs7794745, but not PCDHA rs251379, are associated with the risk of childhood ASD in a Chinese Han population. In addition, rs7794745 in CNTNAP2 was significantly associated with severity of language impairment in autistic children.
The datasets used during the current study are available from the corresponding author on reasonable request.
This wok was presented in part at the 19th WCP World Congress of Psychiatry Meeting, August 2019, Lisbon, Portugal (Jun Liu; Zengyu Zhang; Hong Yu; Jiangying Kong; Zhuo Liu (2019) Association of Genetic Variants in DUSP15, CNTNAP2, and PCDHA Genes and the Risk of Autism Spectrum Disorder) (doi:10.26226/morressier.5d1a036257558b317a13f861).
Conflicts of Interest
The authors have declared no conflicts of interests with respect to the research, authorship, and/or publication of this article.
We are also grateful for the technical assistance from Drs. Jiangying Kong and Zhuo Liu. This work was supported by grants from the Science Technology Department of Zhejiang Province (LGF19H090004) and Xiaoshan District Science and Technology Bureau of Hangzhou City (2018220 and 2019215).
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