Researchers discover a new form of hereditary osteoporosis

Researchers discover a new form of hereditary osteoporosis
Bone health of the study participants was evaluated by radiographs (A, B) and bone biopsy samples (C, D). The patients had in childhood e.g. recurrent forearm fractures (A) and spinal compression fractures (B). Histological evaluation of the bone biopsies showed (C) that bone structure (green) especially in the cortical bone was abnormally fragile and osteoporotic. More detailed evaluation of the bone biopsies showed that the degree of bone mineralization was reduced and the bone tissue was porous (D), leading to reduced bone strength. Credit: Outi Mäkitie Lab

A research group headed by Professor Outi Mäkitie, University of Helsinki, identified in families with childhood-onset osteoporosis disease-causing mutations in a gene that had previously not been connected with the skeletal system or osteoporosis.

"Through extensive genetic research, we identified a underlying osteoporosis in two Finnish families with several affected family members. In collaboration with Dutch and American researchers, we found four additional families with mutations in the same gene resulting in either osteoporosis – as in the Finnish patients – or an even more serious disease associated with severe short stature and disturbed bone development," Mäkitie explains.

"Mutations of the gene SGMS2 were identified as the cause of the disease. SGMS2 encodes an enzyme involved in sphingolipid metabolism; mutations lead to changes in the enzyme function and – through mechanisms so far partially unknown – a serious disturbance of bone metabolism and mineralisation," says Minna Pekkinen, Ph.D., one of the principal investigators in the study.

Mutation carriers had, since childhood, suffered fractures in their limbs and spine even as a result of minor injuries. Certain study subjects also presented , transient facial nerve paralysis being a particularly common one, which, according to Mäkitie, may be one of the distinctive features of this form of osteoporosis.

The examination of bone samples collected from three patients demonstrated that their bone tissue differed from normal : the number of bone cells was atypical and bone mineralisation was disturbed. The changes were particularly clear in the cortical bone – the outer layer of bone – the region with the most abundant expression of the SGMS2 gene.

"This gene finding of ours is very important, as it significantly increases understanding of the mechanisms underlying osteoporosis and opens new avenues for the development of osteoporosis diagnostics and drug therapies," Mäkitie states.

Osteoporosis is characterised by low bone mineral density and deteriorated bone microstructure, expressed as increased bone fragility and proneness to fractures. According to current knowledge, are among the key factors that determine bone strength. However, researchers have so far identified only a handful of genes with a significant effect on the risk of bone loss whose cause familial osteoporosis.

Mäkitie's research group, active at the University of Helsinki, the New Children's Hospital of the Hospital District of Helsinki and Uusimaa and the Folkhälsan Research Centre, is investigating the causes of childhood-onset osteoporosis and, in particular, gene defects that predispose individuals to osteoporosis. Previously, the group identified one new form of (Laine CM et al. NEJM 2013).

More information: Minna Pekkinen et al. Osteoporosis and skeletal dysplasia caused by pathogenic variants in SGMS2, JCI Insight (2019). DOI: 10.1172/jci.insight.126180

Christine M. Laine et al. WNT1 Mutations in Early-Onset Osteoporosis and Osteogenesis Imperfecta, New England Journal of Medicine (2013). DOI: 10.1056/NEJMoa1215458

Citation: Researchers discover a new form of hereditary osteoporosis (2019, February 25) retrieved 25 February 2024 from
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