Osteogenesis Imperfecta Panel

Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous skeletal disorder characterized by frequent bone fractures with or without minimal trauma. Clinical signs of OI can range from mild to severe. In addition to bone fractures, patients may have scoliosis, bowing of long bones, short stature, blue sclera, hearing loss, dentin defects, muscle weakness or joint laxity. Bone fractures and bowing of long bones in osteogenesis imperfecta patients may occur prenatally in severe OI cases, and hearing loss may occur in ~50% of type I OI patients by 40-years-old (https://emedicine.medscape.com/article/947588-overview). The incidence is approximately 6/100,000 (van Dijk et al. 2012. PubMed ID: 21829228). Approximately 90% of clinically diagnosed OI is caused by pathogenic variants in the COL1A1 and COL1A2 genes, while ~10% is caused by pathogenic variants in the BMP1, CREB3L1, CRTAP, FKBP10, IFITM5, P3H1(also called as LEPRE1), PLOD2, PPIB, SEC24D, SERPINF1, SERPINH1, SP7, WNT1, TMEM38B NTRK1 and other undefined genes (van Dijk and Sillence. 2014. PubMed ID: 24715559; Valadares et al. 2014. PubMed ID: 25046257; Moosa et al. 2015. PubMed ID: 26467156; Caparros-Martin et al. 2017. PubMed ID: 28116328).

Genes Related to Autosomal Dominant OI: Pathogenic variants in the COL1A1, COL1A2, and IFITM5 genes cause autosomal dominant OI. More than 95% of pathogenic variants in the COL1A1 and COL1A2 genes are nucleotide substitutions or small deletions or insertions, 1% -2% of COL1A1 and COL1A2 pathogenic variants are larger deletions or insertions (van Dijk and Sillence. 2014. PubMed ID: 24715559; Steiner and Basel. 2019. PubMed ID: 20301472). Almost all perinatal lethal OI are caused by de novo variants in COL1A1 and COL1A2 (Steiner and Basel. 2019. PubMed ID: 20301472).

Genes Related to Autosomal Recessive OI: Pathogenic variants in the BMP1, CREB3L1, CRTAP, FKBP10, P3H1 (also called LEPRE1), PLOD2, PPIB, SEC24D, SERPINF1, SERPINH1, SP7, TMEM38B, TENT5A, MBTPS2, NBAS, SLC2A2, SPARC, TAPT1 and NTRK1 genes cause autosomal recessive OI.

Recently, pathogenic variants in TENT5A (Doyard. 2018. PubMed ID: 29358272), NBAS (Balasubramanian et al. 2017. PubMed ID: 27789416), SLC2A2 (Caparros-Martin et al. 2017. PubMed ID: 28116328), SPARC (Mendoza-Londono et al. 2015. PubMed ID: 26027498), and TAPT1 (Symoens et al. 2015. PubMed ID: 26365339) have been reported in a few patients with autosomal recessive osteogenesis imperfecta.

Pathogenic variants in the XYLT2 gene have been reported in patients with autosomal recessive Spondyloocular syndrome (Taylan et al. 2016. PubMed ID: 26987875), which is characterized by spinal and long bone fractures, osteoporosis, cataract, hearing impairment, cardiac septal defects, and learning difficulties.

Genes related to both autosomal dominant and autosomal recessive OI: WNT1 pathogenic variants mainly cause autosomal recessive OI, but WNT1 has also been reported to be associated with autosomal dominant OI in rare cases.

Pathogenic variants in LRP5 cause autosomal recessive osteoporosis-pseudoglioma syndrome, autosomal dominant Osteopetrosis, type1 and autosomal bone mineral density variability 1.

Genes Related to X-linked OI: Pathogenic variants in PLS3 cause X-linked Bone mineral density QTL18 osteoporosis.

Pathogenic variants in MBTPS2 were reported to be associated with X-linked osteogenesis imperfecta (Lindert et al. 2016. PubMed ID: 27380894).

See individual gene summaries for more information about molecular biology of gene products and spectra of pathogenic variants.

Pathogenic variants in COL1A1 and COL1A2 were found in 90% of individuals with Osteogenesis Imperfecta (OI) types I, II, III, or IV (Steiner and Basel. 2019. PubMed ID: 20301472). A recent study reported that COL1A1 and COL1A2 pathogenic variants were identified in 56% (14/35) and 44% (11/35) of the OI cases, respectively (Stephen et al. 2014. PubMed ID: 24668929).

Only one large homozygous deletion involving CREB3L1 was reported in a patient affected with autosomal recessive OI (Symoens et al. 2013. PubMed ID: 24079343).

CRTAP pathogenic variants were identified in 1 out of 10 clinically diagnosed autosomal recessive OI families (Caparrós-Martin et al. 2013. PubMed ID: 23613367).

In one publication, FKBP10 pathogenic variants were identified in 21 families affected with either autosomal recessive OI or Bruck syndrome (Schwarze et al. 2013. PubMed ID: 22949511). The pathogenic variant detection rate should be high, because all reported FKBP10 pathogenic variants are point variants or small deletions and insertions, which can be detected by sequencing.

So far, only two pathogenic IFITM5 variants have been reported (Guillén-Navarro et al. 2014. PubMed ID: 24478195). The clinical sensitivity should be high for patients with clinically diagnosed OI type V. The c.-14C>T IFITM5 pathogenic variant was found in almost all clinically diagnosed OI Type V patients tested (Lazarus et al. 2014. PubMed ID: 24674092; Human Gene Mutation Database).

P3H1 pathogenic variants were identified in 2 out of 10 clinically diagnosed autosomal recessive OI families (Caparrós-Martin et al. 2013. PubMed ID: 23613367).

SERPINF1 pathogenic variants were identified in 3 out of 10 clinically diagnosed autosomal recessive OI families (Caparrós-Martin et al. 2013. PubMed ID: 23613367).

SERPINH1 pathogenic variants were identified in 1 out of 30 individuals who tested negative for pathogenic variants in COL1A1, COL1A2, CRTAP and LEPRE1 (Christiansen et al. 2010. PubMed ID: 20188343).

So far, only one pathogenic SP7 pathogenic variant, a small deletion, has been reported (Lapunzina et al. 2010. PubMed ID: 20579626).

WNT1 pathogenic variants were reported in 5 out of 12 OI families in which no pathogenic variants in other OI-related genes were found (Keupp et al. 2013. PubMed ID: 23499309).

PLOD2 pathogenic variants were identified in 4 out of 6 clinically diagnosed, consanguineous, unrelated Egyptian families affected with Bruck syndrome type 2 (Puig-Hervás et al. 2012. PubMed ID: 22689593).

Recently, a homozygous missense variant in the NTRK1 gene has been reported in one patient from a consanguineous family with OI-related features (Caparros-Martin et al. 2017. PubMed ID: 28116328).

This test is performed using Next-Gen sequencing with additional Sanger sequencing as necessary.

This panel typically provides 99.9% coverage of all coding exons of the genes plus 10 bases of flanking noncoding DNA in all available transcripts along with other non-coding regions in which pathogenic variants have been identified at PreventionGenetics or reported elsewhere. We define coverage as ≥20X NGS reads or Sanger sequencing. PGnome panels typically provide slightly increased coverage over the PGxome equivalent. PGnome sequencing panels have the added benefit of additional analysis and reporting of deep intronic regions (where applicable).

Dependent on the sequencing backbone selected for this testing, discounted reflex testing to any other similar backbone-based test is available (i.e., PGxome panel to whole PGxome; PGnome panel to whole PGnome).