{"title":"婴儿小头畸形:土耳其的一项回顾性队列研究。","authors":"Gonca Keskindemirci, Öykü Özbörü Aşkan, Burak Selver, Alev Bakır Kayı, Gülbin Gökçay","doi":"10.4274/jcrpe.galenos.2024.2023-5-3","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Microcephaly (MC) is a clinical finding mostly reflecting deficiency of brain growth. The aim of this retrospective cohort study was to assess risk factors and follow-up features of children with MC.</p><p><strong>Methods: </strong>Children’s personal health records (n=7580) followed between 2002 and 2020 in the Unit of a Well Child Clinic were assessed retrospectively. The case group comprised children with MC. MC was defined as head circumference (HC) standard deviation score (SDS) value ≤-2 SDS. Age and sex-matched children with normal HC were selected as the control group.</p><p><strong>Results: </strong>Children with MC (n=49) had more disadvantaged sociodemographic characteristics, such as young maternal and paternal age and low maternal and paternal education. Breastfeeding was more common among controls (n=98). Resolution of MC was observed in 26 (53.1%) children with MC, whether it was mild (HC SDS between -2 and -2.9) or severe (HC SDS ≤3). Children with persistent MC had poorer developmental milestones than controls and cases with resolution. Sociodemographic features or developmental milestones in mild and severe MC did not differ.</p><p><strong>Conclusion: </strong>These results suggest that the use of a definition of MC of ≤-2 SDS would be appropriate in order not to miss cases on follow-up. Greater sociodemographic equality may prevent some cases of MC. Further studies are needed evaluating socioeconomic factors on MC.</p>","PeriodicalId":48805,"journal":{"name":"Journal of Clinical Research in Pediatric Endocrinology","volume":" ","pages":"168-176"},"PeriodicalIF":1.5000,"publicationDate":"2024-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11590720/pdf/","citationCount":"0","resultStr":"{\"title\":\"Microcephaly in Infants: A Retrospective Cohort Study from Turkey\",\"authors\":\"Gonca Keskindemirci, Öykü Özbörü Aşkan, Burak Selver, Alev Bakır Kayı, Gülbin Gökçay\",\"doi\":\"10.4274/jcrpe.galenos.2024.2023-5-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Microcephaly (MC) is a clinical finding mostly reflecting deficiency of brain growth. The aim of this retrospective cohort study was to assess risk factors and follow-up features of children with MC.</p><p><strong>Methods: </strong>Children’s personal health records (n=7580) followed between 2002 and 2020 in the Unit of a Well Child Clinic were assessed retrospectively. The case group comprised children with MC. MC was defined as head circumference (HC) standard deviation score (SDS) value ≤-2 SDS. Age and sex-matched children with normal HC were selected as the control group.</p><p><strong>Results: </strong>Children with MC (n=49) had more disadvantaged sociodemographic characteristics, such as young maternal and paternal age and low maternal and paternal education. Breastfeeding was more common among controls (n=98). Resolution of MC was observed in 26 (53.1%) children with MC, whether it was mild (HC SDS between -2 and -2.9) or severe (HC SDS ≤3). Children with persistent MC had poorer developmental milestones than controls and cases with resolution. Sociodemographic features or developmental milestones in mild and severe MC did not differ.</p><p><strong>Conclusion: </strong>These results suggest that the use of a definition of MC of ≤-2 SDS would be appropriate in order not to miss cases on follow-up. Greater sociodemographic equality may prevent some cases of MC. 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引用次数: 0
摘要
目的:小头畸形(MC)是一种临床表现,主要反映大脑发育不良。我们的研究旨在评估MC患儿的风险因素和随访特征:方法:回顾性评估2002年至2020年期间在健康儿童门诊部随访的儿童个人健康记录(n=7580)。病例组包括 MC 患儿(49 人)。年龄和性别匹配、头围正常的儿童为对照组(98 名)。MC的定义是头围SDS值≤-2 SDS:在这项回顾性队列研究中,MC患儿的社会人口学特征更为不利,如母亲和父亲年龄较小、母亲和父亲受教育程度较低。对照组中母乳喂养率较高。在26名患有MC的儿童中,无论是轻度(头围SDS在-2和-2.9之间)还是重度(头围SDS≤3),都观察到了MC症状的缓解。与对照组和症状缓解的病例相比,患有持续性 MC 的儿童发育里程碑较差。轻度和重度MC患儿的社会人口学特征或发育里程没有统计学差异:根据我们的研究结果,使用头围≤2 SDS来定义MC是合适的,这样可以避免在随访中遗漏病例。一些 MC 病例可以通过减少不平等来预防。还需要进一步研究评估社会经济因素对 MC 的影响。
Microcephaly in Infants: A Retrospective Cohort Study from Turkey
Objective: Microcephaly (MC) is a clinical finding mostly reflecting deficiency of brain growth. The aim of this retrospective cohort study was to assess risk factors and follow-up features of children with MC.
Methods: Children’s personal health records (n=7580) followed between 2002 and 2020 in the Unit of a Well Child Clinic were assessed retrospectively. The case group comprised children with MC. MC was defined as head circumference (HC) standard deviation score (SDS) value ≤-2 SDS. Age and sex-matched children with normal HC were selected as the control group.
Results: Children with MC (n=49) had more disadvantaged sociodemographic characteristics, such as young maternal and paternal age and low maternal and paternal education. Breastfeeding was more common among controls (n=98). Resolution of MC was observed in 26 (53.1%) children with MC, whether it was mild (HC SDS between -2 and -2.9) or severe (HC SDS ≤3). Children with persistent MC had poorer developmental milestones than controls and cases with resolution. Sociodemographic features or developmental milestones in mild and severe MC did not differ.
Conclusion: These results suggest that the use of a definition of MC of ≤-2 SDS would be appropriate in order not to miss cases on follow-up. Greater sociodemographic equality may prevent some cases of MC. Further studies are needed evaluating socioeconomic factors on MC.
期刊介绍:
The Journal of Clinical Research in Pediatric Endocrinology (JCRPE) publishes original research articles, reviews, short communications, letters, case reports and other special features related to the field of pediatric endocrinology. JCRPE is published in English by the Turkish Pediatric Endocrinology and Diabetes Society quarterly (March, June, September, December). The target audience is physicians, researchers and other healthcare professionals in all areas of pediatric endocrinology.