Maggie Kettler, Brittany Simpson, Jareen Meinzen-Derr, Carrie Atzinger, Courtney Hannum, Daniel Choo, Lauren Buck, Lucy Marchesci
{"title":"CHARGE综合征患者听力损失的遗传和临床预测因素","authors":"Maggie Kettler, Brittany Simpson, Jareen Meinzen-Derr, Carrie Atzinger, Courtney Hannum, Daniel Choo, Lauren Buck, Lucy Marchesci","doi":"10.3766/jaaa.230055","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> CHARGE syndrome (CS) is a genetic disorder caused by pathogenic variants within chromodomain helicase DNA-binding protein 7 (<i>CHD7</i>). The classical presentation includes <i>c</i>oloboma, congenital <i>h</i>eart defects, <i>a</i>tresia of the choanae, <i>r</i>etardation of development, <i>g</i>enital hypoplasia, and <i>e</i>ar anomalies. Clinical presentation varies widely by type and severity. Structural anomalies of the ear cause hearing loss in 93 percent of individuals with CS. Factors to predict the type and degree of hearing loss among individual patients with CS have not been identified. Identifying factors would ensure patients receive early intervention and allow health care providers to accurately counsel on expectations. <b>Research Design:</b> To identify factors correlated with certain types and degrees of hearing loss, a retrospective chart review of 57 pediatric individuals with <i>CHD7</i> disease-causing variants from the CHARGE Center at Cincinnati Children's Hospital Medical Center was conducted. All data were manually extracted from participants' medical records, as well as the CHARGE Clinic REDcap database. Type and degree of hearing loss were compared to the type of <i>CHD7</i> variant and craniofacial anomalies. <b>Results:</b> Within our cohort, 97 percent of individuals experienced hearing loss (HL), with sensorineural (SNHL) being the most common type. Eighty-three percent experienced severe-to-profound HL in at least one ear, a higher prevalence than previously reported. Temporal bone scan results were available for 34 participants with HL, and structural anomalies were seen in 79 percent of individuals. Type of HL did correlate with <i>CHD7</i> variant type (n = 100, p = 0.002). The most striking relationship is an increased risk of SNHL with <i>CHD7</i> haploinsufficiency due to nonsense or frameshift variants. <b>Conclusions:</b> Regardless of the type or location of <i>CHD7</i> variant, patients with CS are at risk for HL and should undergo temporal bone analysis as part of their initial workup. Such findings continue to expand providers' understanding of CS and will improve the management of patients.</p>","PeriodicalId":50021,"journal":{"name":"Journal of the American Academy of Audiology","volume":" ","pages":"45-52"},"PeriodicalIF":1.2000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12181062/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genetic and Clinical Predictors of Hearing Loss Among Patients with CHARGE Syndrome.\",\"authors\":\"Maggie Kettler, Brittany Simpson, Jareen Meinzen-Derr, Carrie Atzinger, Courtney Hannum, Daniel Choo, Lauren Buck, Lucy Marchesci\",\"doi\":\"10.3766/jaaa.230055\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Objective:</b> CHARGE syndrome (CS) is a genetic disorder caused by pathogenic variants within chromodomain helicase DNA-binding protein 7 (<i>CHD7</i>). The classical presentation includes <i>c</i>oloboma, congenital <i>h</i>eart defects, <i>a</i>tresia of the choanae, <i>r</i>etardation of development, <i>g</i>enital hypoplasia, and <i>e</i>ar anomalies. Clinical presentation varies widely by type and severity. Structural anomalies of the ear cause hearing loss in 93 percent of individuals with CS. Factors to predict the type and degree of hearing loss among individual patients with CS have not been identified. Identifying factors would ensure patients receive early intervention and allow health care providers to accurately counsel on expectations. <b>Research Design:</b> To identify factors correlated with certain types and degrees of hearing loss, a retrospective chart review of 57 pediatric individuals with <i>CHD7</i> disease-causing variants from the CHARGE Center at Cincinnati Children's Hospital Medical Center was conducted. All data were manually extracted from participants' medical records, as well as the CHARGE Clinic REDcap database. Type and degree of hearing loss were compared to the type of <i>CHD7</i> variant and craniofacial anomalies. <b>Results:</b> Within our cohort, 97 percent of individuals experienced hearing loss (HL), with sensorineural (SNHL) being the most common type. Eighty-three percent experienced severe-to-profound HL in at least one ear, a higher prevalence than previously reported. Temporal bone scan results were available for 34 participants with HL, and structural anomalies were seen in 79 percent of individuals. Type of HL did correlate with <i>CHD7</i> variant type (n = 100, p = 0.002). The most striking relationship is an increased risk of SNHL with <i>CHD7</i> haploinsufficiency due to nonsense or frameshift variants. <b>Conclusions:</b> Regardless of the type or location of <i>CHD7</i> variant, patients with CS are at risk for HL and should undergo temporal bone analysis as part of their initial workup. 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引用次数: 0
摘要
目的:CHARGE综合征(CS)是一种由染色质解旋酶dna结合蛋白7 (CHD7)致病性变异引起的遗传性疾病。典型的表现包括结肠、先天性心脏缺陷、输卵管闭锁、发育迟缓、生殖器发育不全和子宫异常。临床表现因类型和严重程度而异。耳部结构异常导致93%的CS患者听力损失。预测单个CS患者听力损失类型和程度的因素尚未确定。确定因素将确保患者得到早期干预,并允许卫生保健提供者准确地就期望提供咨询。研究设计:为了确定与某些类型和程度的听力损失相关的因素,我们对来自辛辛那提儿童医院医学中心charge中心的57名CHD7致病变异儿童进行了回顾性研究。所有数据均手动从参与者的医疗记录以及CHARGE Clinic REDcap数据库中提取。将听力损失的类型和程度与CHD7变异类型和颅面异常进行比较。结果:在我们的队列中,97%的个体经历过听力损失(HL),其中感音神经性(SNHL)是最常见的类型。83%的患者至少有一只耳朵患有重度至重度HL,患病率高于先前报道。34名HL患者的颞骨扫描结果显示,79%的患者出现结构异常。HL类型与CHD7变异类型相关(n = 100, p = 0.002)。最显著的关系是由于无义或移码变异导致的CHD7单倍不足增加SNHL的风险。结论:无论CHD7变异的类型或位置如何,CS患者都有HLand的风险,应将颞骨分析作为其初始检查的一部分。这些发现继续扩大了提供者对CS的理解,并将改善患者的管理。
Genetic and Clinical Predictors of Hearing Loss Among Patients with CHARGE Syndrome.
Objective: CHARGE syndrome (CS) is a genetic disorder caused by pathogenic variants within chromodomain helicase DNA-binding protein 7 (CHD7). The classical presentation includes coloboma, congenital heart defects, atresia of the choanae, retardation of development, genital hypoplasia, and ear anomalies. Clinical presentation varies widely by type and severity. Structural anomalies of the ear cause hearing loss in 93 percent of individuals with CS. Factors to predict the type and degree of hearing loss among individual patients with CS have not been identified. Identifying factors would ensure patients receive early intervention and allow health care providers to accurately counsel on expectations. Research Design: To identify factors correlated with certain types and degrees of hearing loss, a retrospective chart review of 57 pediatric individuals with CHD7 disease-causing variants from the CHARGE Center at Cincinnati Children's Hospital Medical Center was conducted. All data were manually extracted from participants' medical records, as well as the CHARGE Clinic REDcap database. Type and degree of hearing loss were compared to the type of CHD7 variant and craniofacial anomalies. Results: Within our cohort, 97 percent of individuals experienced hearing loss (HL), with sensorineural (SNHL) being the most common type. Eighty-three percent experienced severe-to-profound HL in at least one ear, a higher prevalence than previously reported. Temporal bone scan results were available for 34 participants with HL, and structural anomalies were seen in 79 percent of individuals. Type of HL did correlate with CHD7 variant type (n = 100, p = 0.002). The most striking relationship is an increased risk of SNHL with CHD7 haploinsufficiency due to nonsense or frameshift variants. Conclusions: Regardless of the type or location of CHD7 variant, patients with CS are at risk for HL and should undergo temporal bone analysis as part of their initial workup. Such findings continue to expand providers' understanding of CS and will improve the management of patients.
期刊介绍:
The Journal of the American Academy of Audiology (JAAA) is the Academy''s scholarly peer-reviewed publication, issued 10 times per year and available to Academy members as a benefit of membership. The JAAA publishes articles and clinical reports in all areas of audiology, including audiological assessment, amplification, aural habilitation and rehabilitation, auditory electrophysiology, vestibular assessment, and hearing science.