Search Results

You are looking at 1 - 1 of 1 items for

  • Author: Juha Kere x
Clear All Modify Search
Tian Cheng Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden

Search for other papers by Tian Cheng in
Google Scholar
PubMed
Close
,
Elisabet Einarsdottir Department of Gene Technology, School of Engineering Sciences in Chemistry, Biotechnology and Health, Royal Institute of Technology, Stockholm, Sweden

Search for other papers by Elisabet Einarsdottir in
Google Scholar
PubMed
Close
,
Juha Kere Department of Biosciences and Nutrition (BioNut), Karolinska Institutet, Stockholm, Sweden
Folkhälsan Research Center, Helsinki, Finland

Search for other papers by Juha Kere in
Google Scholar
PubMed
Close
, and
Paul Gerdhem Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institutet, Stockholm, Sweden
Department of Reconstructive Orthopaedics, Karolinska University Hospital, Stockholm, Sweden

Search for other papers by Paul Gerdhem in
Google Scholar
PubMed
Close

Purpose

  • 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.

Methods

  • 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).

Results

  • 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).

Conclusion

  • 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.

Open access