Cheng Tian, Einarsdottir Elisabet, Kere Juha, Gerdhem Paul
Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden.
Department of Gene Technology, School of Engineering Sciences in Chemistry, Biotechnology and Health, Royal Institute of Technology, Stockholm, Sweden.
EFORT Open Rev. 2022 May 31;7(6):414-421. doi: 10.1530/EOR-22-0026.
Idiopathic scoliosis is the most common spinal deformity and affects 1-3% of children and adolescents. Idiopathic scoliosis may run in families and the purpose of this systematic review was to describe the degree of heritability.
We searched Medline, Web of Science and EMBASE for family and twin studies reporting heritability estimates for idiopathic scoliosis, or studies from which heritability estimates could be calculated. Reference lists were screened for additional papers. We followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. The protocol was registered at PROSPERO (registration number: CRD42022307329).
The literature search identified 1134 reports. After full-text screening, nine eligible reports were included for data extraction. Seven were twin studies containing between 5 and 526 pairs, and two were family studies with 1149 and 2732 individuals, respectively. Quality was 'good' in four studies and 'fair' in five studies. In general, studies with radiograph-confirmed diagnosis reported higher heritability estimates than studies with self-reported diagnosis. Population-based twin studies reported lower heritability estimates than clinic-based twin studies. Family-based studies reported higher heritability estimates than twin studies. Pairwise concordance for scoliosis ranged from 0.11 to 1.00 in monozygotic twins and from 0 to 1.0 in dizygotic twins. A meta-analysis of three studies resulted in a narrow sense heritability estimate of 0.57 (95% CI: 0.29-0.86).
Twin and family studies indicate a hereditary component in idiopathic scoliosis, but study heterogeneity is large, and the degree of the heritability is uncertain. Nevertheless, known genetic variants associated with idiopathic scoliosis can still only explain a minor part of heritability.
特发性脊柱侧凸是最常见的脊柱畸形,影响1%至3%的儿童和青少年。特发性脊柱侧凸可能具有家族遗传性,本系统评价的目的是描述其遗传度。
我们检索了Medline、科学网和EMBASE,查找报告特发性脊柱侧凸遗传度估计值的家族和双生子研究,或可计算遗传度估计值的研究。对参考文献列表进行筛查以寻找其他论文。我们遵循系统评价和Meta分析的首选报告项目指南。该方案已在国际前瞻性系统评价注册库(PROSPERO)注册(注册号:CRD42022307329)。
文献检索共识别出1134篇报告。经过全文筛选,纳入9篇符合条件的报告进行数据提取。7篇为双生子研究,包含5至526对双生子,2篇为家族研究,分别涉及1149人和2732人。4项研究质量为“良好”,5项研究质量为“中等”。总体而言,经X线片确诊的研究报告的遗传度估计值高于自我报告诊断的研究。基于人群的双生子研究报告的遗传度估计值低于基于临床的双生子研究。基于家族的研究报告的遗传度估计值高于双生子研究。单卵双生子脊柱侧凸的成对一致性范围为0.11至1.00,双卵双生子为0至1.0。对3项研究进行的Meta分析得出狭义遗传度估计值为0.57(95%CI:0.29 - 0.86)。
双生子和家族研究表明特发性脊柱侧凸存在遗传因素,但研究异质性较大,遗传度程度尚不确定。然而,已知的与特发性脊柱侧凸相关的基因变异仍只能解释遗传度的一小部分。