Genetic testing for diagnosing neurodevelopmental disorders and epilepsy: a systematic review and meta-analysis
Abstract Background Identifying the genetic causes of neurodevelopmental disorders (NDDs) and epilepsy is crucial for effective treatment and genetic counseling. Our objective was to determine the diagnostic yield of chromosomal microarray (CMA) and next-generation sequencing (NGS) methods—including...
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2025-07-01
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| Online Access: | https://doi.org/10.1186/s13643-025-02896-y |
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| author | Yu-Ming Chang Yen-Ta Huang Pei-Chun Lai |
| author_facet | Yu-Ming Chang Yen-Ta Huang Pei-Chun Lai |
| author_sort | Yu-Ming Chang |
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| description | Abstract Background Identifying the genetic causes of neurodevelopmental disorders (NDDs) and epilepsy is crucial for effective treatment and genetic counseling. Our objective was to determine the diagnostic yield of chromosomal microarray (CMA) and next-generation sequencing (NGS) methods—including targeted sequencing (TS), whole-exome sequencing (WES), and whole-genome sequencing (WGS)—in individuals with NDDs or epilepsy. Methods We systematically searched PubMed, Embase, and the Cochrane Library through August 31, 2024. Two reviewers independently screened studies and extracted data. We included studies with ≥ 10 patients (probands) diagnosed with an NDD or epilepsy who underwent CMA, TS, WES, WGS, or WES reanalysis. Methodological quality was assessed using the Newcastle–Ottawa Scale (NOS). Random-effects meta-analysis was performed to pool diagnostic yield percentages. Subgroup analyses were conducted by test modality, disorder subtype, and clinical features. Results A total of 416 studies (124,937 participants) met inclusion criteria. Pooled analysis showed significantly higher diagnostic yields with NGS methods compared to CMA (31.1% vs 14.8% in NDD cohorts; 28.7% vs 13.3% in epilepsy cohorts). Within NGS, WES had a higher yield than targeted gene panels (35.3% vs. 23.2% for NDDs; 34.2% vs. 24.0% for epilepsy). Diagnostic yields increased over time in more recent studies. Patients with certain clinical features had particularly high yields: NDDs with dysmorphic features (54.7%), syndromic presentations (37.6%), or co-occurring epilepsy (35.6%), and epilepsy with early onset (32.3%), epileptic encephalopathy (34.7%), or drug-resistant seizures (25.4%). Quality assessment using NOS revealed that the majority of included studies were of good to very good methodological quality. Conclusions Despite substantial between-study heterogeneity and variability in study designs that may limit the certainty of our pooled estimates, and potential publication bias, our results demonstrate that NGS-based tests—particularly WES and WGS—provide markedly higher diagnostic yields in patients with NDDs or epilepsy compared to CMA, supporting their use as first-line genetic tests. Patients with dysmorphism, syndromic NDD, early-onset or refractory epilepsy, and epileptic encephalopathy achieve above-average diagnostic yields, highlighting the value of comprehensive genetic testing in these subgroups. Systematic review registration PROSPERO CRD42024555664. |
| format | Article |
| id | doaj-art-e4ddaa0f697e477ab1e1f05ab5124dd4 |
| institution | Kabale University |
| issn | 2046-4053 |
| language | English |
| publishDate | 2025-07-01 |
| publisher | BMC |
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| series | Systematic Reviews |
| spelling | doaj-art-e4ddaa0f697e477ab1e1f05ab5124dd42025-08-20T03:45:48ZengBMCSystematic Reviews2046-40532025-07-0114111110.1186/s13643-025-02896-yGenetic testing for diagnosing neurodevelopmental disorders and epilepsy: a systematic review and meta-analysisYu-Ming Chang0Yen-Ta Huang1Pei-Chun Lai2Department of Genetic and Genomic Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung UniversityDepartment of Surgery, College of Medicine, National Cheng Kung University Hospital, National Cheng Kung UniversityDepartment of Pediatrics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung UniversityAbstract Background Identifying the genetic causes of neurodevelopmental disorders (NDDs) and epilepsy is crucial for effective treatment and genetic counseling. Our objective was to determine the diagnostic yield of chromosomal microarray (CMA) and next-generation sequencing (NGS) methods—including targeted sequencing (TS), whole-exome sequencing (WES), and whole-genome sequencing (WGS)—in individuals with NDDs or epilepsy. Methods We systematically searched PubMed, Embase, and the Cochrane Library through August 31, 2024. Two reviewers independently screened studies and extracted data. We included studies with ≥ 10 patients (probands) diagnosed with an NDD or epilepsy who underwent CMA, TS, WES, WGS, or WES reanalysis. Methodological quality was assessed using the Newcastle–Ottawa Scale (NOS). Random-effects meta-analysis was performed to pool diagnostic yield percentages. Subgroup analyses were conducted by test modality, disorder subtype, and clinical features. Results A total of 416 studies (124,937 participants) met inclusion criteria. Pooled analysis showed significantly higher diagnostic yields with NGS methods compared to CMA (31.1% vs 14.8% in NDD cohorts; 28.7% vs 13.3% in epilepsy cohorts). Within NGS, WES had a higher yield than targeted gene panels (35.3% vs. 23.2% for NDDs; 34.2% vs. 24.0% for epilepsy). Diagnostic yields increased over time in more recent studies. Patients with certain clinical features had particularly high yields: NDDs with dysmorphic features (54.7%), syndromic presentations (37.6%), or co-occurring epilepsy (35.6%), and epilepsy with early onset (32.3%), epileptic encephalopathy (34.7%), or drug-resistant seizures (25.4%). Quality assessment using NOS revealed that the majority of included studies were of good to very good methodological quality. Conclusions Despite substantial between-study heterogeneity and variability in study designs that may limit the certainty of our pooled estimates, and potential publication bias, our results demonstrate that NGS-based tests—particularly WES and WGS—provide markedly higher diagnostic yields in patients with NDDs or epilepsy compared to CMA, supporting their use as first-line genetic tests. Patients with dysmorphism, syndromic NDD, early-onset or refractory epilepsy, and epileptic encephalopathy achieve above-average diagnostic yields, highlighting the value of comprehensive genetic testing in these subgroups. Systematic review registration PROSPERO CRD42024555664.https://doi.org/10.1186/s13643-025-02896-yNeurodevelopmental disorderEpilepsyNext-generation sequencingChromosomal microarrayGenetic testDiagnostic yield |
| spellingShingle | Yu-Ming Chang Yen-Ta Huang Pei-Chun Lai Genetic testing for diagnosing neurodevelopmental disorders and epilepsy: a systematic review and meta-analysis Systematic Reviews Neurodevelopmental disorder Epilepsy Next-generation sequencing Chromosomal microarray Genetic test Diagnostic yield |
| title | Genetic testing for diagnosing neurodevelopmental disorders and epilepsy: a systematic review and meta-analysis |
| title_full | Genetic testing for diagnosing neurodevelopmental disorders and epilepsy: a systematic review and meta-analysis |
| title_fullStr | Genetic testing for diagnosing neurodevelopmental disorders and epilepsy: a systematic review and meta-analysis |
| title_full_unstemmed | Genetic testing for diagnosing neurodevelopmental disorders and epilepsy: a systematic review and meta-analysis |
| title_short | Genetic testing for diagnosing neurodevelopmental disorders and epilepsy: a systematic review and meta-analysis |
| title_sort | genetic testing for diagnosing neurodevelopmental disorders and epilepsy a systematic review and meta analysis |
| topic | Neurodevelopmental disorder Epilepsy Next-generation sequencing Chromosomal microarray Genetic test Diagnostic yield |
| url | https://doi.org/10.1186/s13643-025-02896-y |
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