Ana Rita Couto1,2†
Bruna Parreira1,2†
Deborah M. Power3Luís Pinheiro4
João Madruga Dias5,6Irina Novofastovski7Iris Eshed8
Piercarlo Sarzi-Puttini9Nicola Pappone10
Fabiola Atzeni11
Jorrit-Jan Verlaan12Jonneke Kuperus13
Amir Bieber7
Pasquale Ambrosino14David Kiefer15Muhammad Asim Khan16Reuven Mader7,17,18
Xenofon Baraliakos18
Jácome Bruges-Armas1,2*Diffuse Idiopathic Skeletal Hyperostosis (DISH) and Ossification of the Posterior Longitudinal Ligament (OPLL) are common disorders characterized by the ossification of spinal ligaments. The cause for this ossification is currently unknown but a genetic contribution has been hypothesized. Over the last decade, many studies on the genetics of ectopic calcification disorders have been performed, mainly on OPLL. Most of these studies were based on linkage analysis and case control association studies. Animal models have provided some clues but so far, the involvement of the identified genes has not been confirmed in human cases. In the last few years, many common variants in several genes have been associated with OPLL. However, these associations have not been at definitive levels of significance and evidence of functional significance is generally modest. The current evidence suggests a multifactorial aetiopathogenesis for DISH and OPLL with a subset of cases showing a stronger genetic component.
The spine is a columnar structure composed of bony vertebrae interconnected by intervertebral discs and supported by ligaments, such as the anterior and posterior longitudinal ligaments, ligament nuchae and ligamentum flavum. The spinal canal, enclosed within the foramen of the vertebrae, contains the spinal cord. In the intervertebral spaces, the canal is protected by the ligament flavum posteriorly and the posterior longitudinal ligament anteriorly. Spinal stenosis consists in the reduction of the area of the spinal canal, leading to motor neuron deficits and related neurological symptoms, depending on the location of the stenosis (Bai et al., 2022). In the elderly population, the most common cause of spinal cord impairment is the degenerative cervical myelopathy (DCM). DCM can be secondary to osteoarthritic degeneration or to ligamentous ossifications such as the Ossification of the Posterior Longitudinal Ligament (OPLL) or the ossification of the Ligament Flavum (OLF) (Nouri et al., 2015). OPLL, frequently in association with DISH, can result in various degrees of neurological complications that can range from a slowly progressive painless myelopathy to a rapid progression of a neurological deficit even after minor injury (Takayuki et al., 2021; Prabhu et al., 2022). The physical and socioeconomic burden of disability associated with DCM is expected to grow evenly, due to the ageing population (Badhiwala et al., 2020). It is thus crucial to improve the diagnosis and assessment of disorders involved in DCM for early detection and swift intervention.
This review will focus on genetic studies of the ossification of the anterior and posterior longitudinal ligaments, the Diffuse Idiopathic Skeletal Hyperostosis (DISH) [MIM: 106400] and the Ossification of the Posterior Longitudinal Ligament (OPLL) [MIM: 602475], respectively. A short outline of DISH, OPLL and OLF can be seen in Table 1. These conditions may co-occur in some patients suggesting possible common etiopathogenic factors (Nouri et al., 2015; Takayuki et al., 2021). The objective was to collect and present evidences that supports a genetic foundation, based on the following observations: 1) familial aggregation reports, 2) animal models, 3) associated genetic variants and 4) genetics of associated disorders.
Table 1. Brief characterization, main symptoms and epidemiology of DISH, OPLL and OLF.
Reports of familial DISH are scarce. Beardwell, A. in 1969 (Beardwell, 1969), describes a family with Ankylosing Vertebral Hyperostosis (AVH), by the third decade, with many family members also presenting tylosis (punctuate hyperkeratosis). As demonstrated by the author, the X-ray of the affected family members showed ossification of paraspinal distribution, mainly in the lower thoracic region and also some osteophytosis and marginal sclerosis of the sacroiliac joints.
Another report of familial DISH, described 2 families; one had 4 siblings showing AVH by the fourth decade and two other family members had probably AVH. The second family was dentified after hip surgery of two sisters aged 71 and 82 years. The proband had five daughters, two of them affected by AVH and other two with a mild phenotype, classified as possible AVH (Abiteboul et al., 1985). An unusual DISH-like phenotype was described in a family with severe cervical disease lacking the extensive dorsal involvement (Gorman et al., 2005).
In Azores region, twelve families were identified presenting early onset (third decade) of DISH and/or Chondrocalcinosis (CC). The affected members had a pyrophosphate arthropathy showing exuberant axial and peripheral enthesopathic calcifications, meaning calcification of the connective tissues in the attachments of tendons or ligaments to the bones, in joints other than the spine (Bruges-Armas et al., 2006). Genetic studies in these families suggest that the phenotype DISH/CC is polygenic and influenced by the interaction of several, small-effect gene variants and possibly by unidentified environmental factors (Couto et al., 2017; Parreira et al., 2020). Similar cases, of patients with CPPD and/or CC and DISH, were mentioned in other studies (Okazaki et al., 1976), also showing familial aggregation (van der Korst et al., 1974; Bruges-Armas et al., 2006).
A postmortem examination of a skeleton allowed the diagnosis of DISH and ankylosing spondylitis in the same patient (Jordana et al., 2009). An extensive radiographic survey on several members of the Medici family (15th–17th century), demonstrated that DISH, rheumatoid arthritis and uric acid gout affected several family members (Fornaciari et al., 2009; Fornaciari and Giuffra, 2013). A study of 13 royal Egyptian mummies detected ossifications at the anterior aspects of the spines in five male mummies but only four fulfilled the criteria for DISH (Saleem and Hawass, 2014).
The cause of OPLL is unclear but people of Asian heritage, have a higher likelihood of developing this condition (Choi et al., 2011). Familial aggregation of cervical OPLL was first demonstrated in a study assessing 347 families (Terayama, 1989); the relative risk of first degree relatives came to have OPLL was five times greater than expected in the general population. Another study shows a prevalence of 27% with a relative risk seven times that of the general population (Tanikawa et al., 1986). Other OPLL familial cases included the report of familial thoracic OPLL in Caucasian siblings (Tanabe et al., 2002) (Terayama, 1989).
The mode of inheritance for OPLL is still poorly defined due to the absence of large families, late onset of the disorder, environmental effects and sex differences (Koga et al., 1998). However, segregation studies shows that OPLL have both autosomal dominant (Tanikawa et al., 1986) and autosomal recessive (Hamanishi et al., 1995) patterns of inheritance. As discussed later, ectopic ossification resembling OPLL, as seen in the tiptoe walking mouse (ttw) or also called tiptoe walking of Yoshimura (twy), is inherited as an autosomal recessive disease with complete penetrance (Ikegawa et al., 2007).
The study of mouse strain models and the progress of strategies to find genetic mutations, affecting the mineralization pattern, have permitted the discovery of many genes and proteins to be evaluated.
Some of the earliest genetic studies were performed on genes belonging to Major Histocompatibility complex, specifically Human Leucocyte Antigens (HLA) (Brewerton et al., 1973; Schlosstein et al., 1973), but this association was never confirmed.
In a small study, polymorphisms of the Collagen Type I Iα1 (COL1A1), and Vitamin D Receptor (VDR) were investigated, but the authors concluded that these genes do not seem to be related to DISH etiology (Havelka et al., 2002). One more study, investigated polymorphisms of the collagen 6A1 gene (COL6A1) in Czech and Japanese DISH patients and the polymorphism, in intron 32, was associated with the disorder in Japanese patients but failed the association test with DISH Czech patients (Table 2). However, the authors suggested that COL6A1 could be related to ectopic bone formation in spinal ligaments (Tsukahara et al., 2005). Due to the possible common aetiopathogenesis of OPLL and DISH, a genotyping study (intron 6; −4) on the COL11A2 gene was performed, and no significant difference was observed between both cohorts (Havelka et al., 2001). Jun et al (Jun and Kim, 2012) described that two polymorphisms in the FGF2 gene were associated with DISH (Table 2). Another study identified a genetic variant in the PPP2R2D gene significantly associated with a phenotype characterized by DISH and CC. It was proposed that PPP2R2D may contribute to the development of this disorder (Parreira et al., 2020). Although these variants are significantly associated with DISH, the direct evidence for pathogenicity is lacking.
Table 2. Genes and genetic variants associated with DISH. The protein physiological function is also mentioned. Gene function was obtained from GeneCards database.
Many genetic studies of OPLL have been performed and it is now well established that genetic factors are implicated in its etiology (Terayama, 1989) (Table 3). In the same way as DISH, the initial genetic studies of OPLL were performed on HLA and the possible association is much discussed in the literature (Sakou et al., 1991; Yamaguchi, 1991; Matsunaga et al., 1999). Very close to the HLA region on the chromosome 6 is COL11A2 and common variants of this gene have been associated with OPLL (Koga et al., 1998; Maeda et al., 2001a). The polymorphism in intron 6 (-4A) seems to confer protection to OPLL furthermore, it was proven that this polymorphism of COL11A2 affects the splicing of exon 6 in cells obtained from spinal ligaments from OPLL patients (Maeda et al., 2001b).
Table 3. Genes and genetic variants associated with OPLL predisposition. The protein physiological function is also mentioned. Protein function was obtained from GeneCards database.
According to Nakamura et al. (1999) the deletion of T, 11 nucleotides upstream of the splice acceptor site of intron 20 (IVS20-11delT) of ENPP1 is associated with OPLL. However, He et al. (2013) described that the polymorphism TT genotype of C973T and IVS15-14T as well as the wild type IVS20 (lack of deletion) were related with disease severity. Another study found a polymorphism (IVS15-14T-- > C) in ENPP1 gene associated with OPLL susceptibility and severity (Koshizuka et al., 2002). Interestingly, in one study the authors found that the ENPP1 variant (IVS20-11delT) and the SNP (A861G) in the leptin receptor gene (LEPR) were more frequent in OPLL patients affected in the thoracic spine compared to patients whose OPLL was restricted to cervical spine. The authors suggested that the two variants (IVS20-11delT and A861G) are associated with more extensive OPLL, but not with frequency of its occurrence (Tahara et al., 2005).
The COL6A1 gene is intensely associated to OPLL and polymorphisms in this gene are considered useful markers of OPLL (Tanaka et al., 2003; Kong et al., 2007; Wang et al., 2018a). However this association is not always confirmed in all the studies performed (Furushima et al., 2002; Liu et al., 2010). Polymorphisms in COL6A1 gene were associated with DISH in the Japanese population (Tsukahara et al., 2005) suggesting that COL6A1 may contribute in pathological ectopic ossification.
Positive associations of BMP2, an important regulator of bone metabolism, with OPLL were found with the SNPs rs3178250 (Wang et al., 2008), rs2273073 (Chen et al., 2008; Yan et al., 2013) and rs1949007 (Chen et al., 2008) (Table 3). Yan et al. (2013), confirmed that the SNP rs227373 in the BMP2 gene is associated with the higher level of Smad4 protein expression and with activity of alkaline phosphatase. On the other hand, according to Kim et al. (2014a) the SNPs rs2273073 and rs1949007, in Korean patients, are not associated with OPLL. Other study (Liu et al., 2010), performed in Chinese Han population, also failed to show association between BMP2 gene and OPLL. A genome-wide linkage study performed with 214 OPLL affected sib-pairs identified a chromosome region (20p12), linked with OPLL (Karasugi et al., 2013). This region contains 25 genes, of which two are good candidates: Jagged 1 (JAG1), which is involved in endochondral bone formation (Nobta et al., 2005) and BMP2. Furthermore, deleterious coding variants of BMP2 in peripheral blood samples was recently demonstrated (Chen et al., 2016). Three other polymorphisms (rs996544, rs965291 and rs1116867) were screened in Han Chinese subjects and the authors found that rs1116867 and rs965291 were related with the manifestation and extend of OPLL (Yan et al., 2010).
Other bone morphogenetic protein genes have been associated with OPLL; two SNPs in BMP-9 were found to be associated with OPLL: rs75024165 and rs34379100 (Ikuma et al., 2022). BMP-4 SNPs rs17563 (Mader et al., 2013; Cudrici et al., 2021), rs76335800 and a specific haplotype, TGGGCTT (Mader et al., 2013), were identified as risk factors for developing OPLL in the Chinese population. Furushima et al. (Ramos et al., 2015) also confirmed the association of BMP-4 with OPLL, in a large scale screening study, in which only BMP-4 reached criteria of suggestive evidence of linkage. In a recent study, BMP-4 has even been proposed as a new therapeutic option for treating bone diseases due to its role on a RUNX2/CHRDLI/BMP4 pathway. Several SNPs in gene RUNX2 have also been associated with OPLL (Liu et al., 2010; Chang et al., 2017).
Another important gene with contradictory results is TGFβ1, that according to Kamiya et al. (2001), is genetically associated to OPLL (869T > C; rs1982073). However, Han et al. (2013) showed that the SNP previously associated with OPLL (rs1982073) and the SNP located in the promoter region (rs1800469) are not associated with OPLL in Korean populations. Interestingly, in the chondrocytes of adjacent cartilaginous areas and in the ossified matrix of OPLL the TGF-β1 gene is overexpressed. The same authors tested the association between rs1982073 and the radiological appearance of OPLL, and they verified that SNP rs1982073 is associated to the specific area of the ossified lesion, and not to the onset of OPLL. The “C” allele could be a risk factor for patients with OPLL in cervical, thoracic, and/or lumbar spine (Kawaguchi et al., 2003).
In relation to ossification of the ligamentum flavum several genes and loci have been associated with thoracic Ossification of Ligamentum Flavum (OLF) (Kong et al., 2007; Liu et al., 2010; Qu et al., 2017; Qu et al., 2021).
The presence of OSL has been described in association with numerous diseases of diverse etiologies. The type of disorders, the main pathways affected and the consequences, including the main anomalies identified in laboratory analysis, are outlined in Figure 1.
Figure 1. Disorders associated with a higher prevalence of OSL. GH: growth hormone, PTH: parathormone, IGF-A: insulin growth factor 1, HGA: homogentisic acid.
The OSL associated disorders can be of endocrine, nutritional or metabolic nature. The main endocrine associated disorders—diabetes mellitus, acromegaly and hypoparathyroidism—are characterized by disturbances in the metabolism of glucose, growth hormone (GH), and parathyroid hormone (PTH), leading to hypocalcemia, hyperphosphatemia, hyperglycemia and hyperinsulinemia. These endocrine anomalies are often linked to obesity, which can also have a strong genetic basis. The excessive intake of fluoride and vitamin A leads to OSL resembling DISH. Disturbances in mineral metabolism namely phosphorus phosphatase and calcium can also originate disorders that have been reported in association with OSL: familial hypocalciuric hypercalcemia, hypophosphatemic rickets and hypophosphatasia.
Table 4 lists a subset of DISH and OPLL cases originated by monogenic disorders. With the exception of alkaptonuria, characterized by the levels of Homogentisic acid, all of the other disorders are directly involved in calcium and phosphate homeostasis. As expected, genes related in hypophosphatemic rickets and hypophosphatasia are directly involved in phosphate homeostasis. However, the reports of OSL are not related to all types of hypophosphatasia disorders. Saito et al. (2011), reported a case of OPLL with hypophosphatemic rickets/osteomalacia caused by a splice donor site mutation in the ENPP1 gene. Cases of hypoparathyroidism associated with changes similar to DISH are also reported in the literature (Lambert and Becker, 1989; Unverdi et al., 2009; John and Suthar, 2016). The genes GNAS, GCM2 and PTH, closely related to hypoparathryroidism, play a role in both calcium and phosphorus metabolism. According to what we know, there is only one case described of a patient with DISH and familial hypocalciuric hypercalcemia (FHH). The patient, a 45-year-old diabetic woman, have hypercalcemia secondary to FHH and developed dysphagia because of external esophageal compression from DISH. According to the authors, the relationship between FHH and DISH remains unproven (Rivas and Lado-Abeal, 2013). Acromegaly is a rare condition of high elevated somatic growth and distorted proportions arising from hypersecretion of growth hormone (GH) and insulin-like growth factor 1 (IGF-1) due to adenomas and pathogenic pituitary secretion (Ben-Shlomo and Melmed, 2008). According to Altomonte et al. (1992), GH levels may act as bone promoting factors in DISH.
Table 4. Monogenic disorders previously associated with OSL. Lack of inheritance means that it is still unconfirmed.
The etiology of “risk-factor” OSL disorders is complex, and determined by the interaction of inherited and environmental factors, such as age, smoking, alcohol consumption, diet and physical inactivity. These factors, as already know, effect type 2 diabetes mellitus (T2D) and obesity, two of the known risk factor for developing DISH. Even though heterogeneous, there are some monogenic forms of these OSL disorders; see Table 5 for more details. Diabetes mellitus is considered to be a heterogeneous group of disorders having as a main characteristic persistent hyperglycemia (Pillai and Littlejohn, 2014). Obesity is considered a complex and a multifactorial disease, however there are monogenic cases reported that are related to mutations in genes of the leptin/melanocortin system involved in food intake regulation (Huvenne et al., 2016). It is interesting to see that genetic variants in LEPR gene, as occurs in the ZFR murine model, can cause obesity, hypercholesterolemia, hyperinsulinemia, hyperlipidemia and also ossification of spinal ligaments, similar to human OPLL (Okano et al., 1997). Furthermore, there are studies reporting increased levels of serum leptin in female patients with OPLL (Ikeda et al., 2011) (Feng et al., 2018) as well as in DISH patients (Tenti et al., 2017). The osteogenic effects of leptin/leptin receptor (LepR) in conjunction with mechanical stress, on the ossification of the posterior ligament, through its interaction with osteogenic markers such as osteopontin, osteocalcin and RUNX2, were also recently shown (Chen et al., 2018). It is also pertinent to mention that ENPP1 is a predisposition gene for both obesity and type 2 diabetes. The importance of leptin/LEPR in disorders such as DISH, with an important metabolic association, remain to be revealed.
Table 5. Complex disorders previously associated with OSL. AD stands for Autosomal Dominant, AR for Autosomal Recessive. Lack of inheritance means that it is not confirmed.
The co-existence of DISH with other rheumatic disorders was first reported in 1950 by Forestier and Rotes Querol (Forrestier, 1950). Subsequent studies indicate, in some cases that up to 50% of DISH patients also have OPLL proposing that they share common etiopathogenic factors. Simultaneous OPLL and OLF are also very common in the literature (Li et al., 2012; Onishi et al., 2016). In addition, the co-existence of the three OSL disorders—DISH; OPLL and OLF has also been described in the literature (Guo et al., 2011). The association of DISH with psoriatic arthritis in the literature (Ben-Shlomo and Melmed, 2008) is common but studies concluded that is a side effect of retinoids treatment (Bologna et al., 1991). Other rheumatic diseases co-existing with DISH include: hyperostosis frontalis interna (Arlet et al., 1978; Mazières et al., 1978; Ciocci et al., 1985; Fukunishi et al., 1987; Fukunishi and Hosokawa, 1988), CPPD and/or CC (Resnick et al., 1978a; Bruges-Armas et al., 2006), gout (Resnick et al., 1978a; Littlejohn and Hall, 1982; Constantz, 1983; Fornaciari et al., 2009), rheumatoid arthritis (Resnick et al., 1978a; Resnick et al., 1978b; Forster et al., 1981; Mata et al., 1995), osteoarthritis (Resnick et al., 1978a), Heberden and Bouchard nodes (Schlapbach et al., 1992) and Paget’s disease (Mazières et al., 1978; Morales et al., 1993).
DISH and Ankylosing Spondylitis (AS) generally have a distinct radiographic appearance but sometimes, possibly in the early disease stages, they are difficult to distinguish radiologically (Williamson and Reginato, 1984; Olivieri et al., 1987; Olivieri et al., 1989; Rillo et al., 1989; Troise Rioda and Ferraccioli, 1990; Olivieri, 1991; Passiu et al., 1991; Maertens et al., 1992; Tishler and Yaron, 1992; Jattiot et al., 1995; Moreno et al., 1996; Kozanoglu et al., 2002; Jordana et al., 2009; Wooten, 2009; Macia-Villa et al., 2016; Kuperus et al., 2018). OPLL has also been observed in patients with AS but this coexistence is probably coincidental (Kim et al., 2007). Chondrocalcinosis, is characterized by the deposition of calcium containing crystals in synovial membranes, articular cartilage and, sometimes it can also affect periarticular soft tissues. Curiously, in some patients, the deposition of calcium crystals—hydroxyapatite or CPPD—can also occur in the spinal ligaments (Resnick and Pineda, 1984; Muthukumar et al., 2000) but this is usually difficult to differentiate from ossification (Ehara et al., 1998). ANKH is the only monogenic cause identified for CC (Table 6); a recent study described a gain-of-function mutation in the gene TNFRSF11B, which resulted in early-onset osteoarthritis and CC (Ramos et al., 2015). A recently described hereditary autosomal recessive ectopic mineralization syndrome in patients with arterial Calcification due to deficiency of CD73 (ACDC), was the result of a loss of function mutations in the 5′-nucleoside Ecto (NT5E) gene. These patients had erosive peripheral arthropathy and axial enthesopathic calcifications, resembling DISH although with decreased disc space height and the presence of large intervertebral disk calcifications (Cudrici et al., 2021). The similarities to both DISH and AS of the outcome of spine imaging of ACDC patients are noteworthy.
Table 6. Rheumatic disorders previously seen coexisting with OSL. AD stands for Autosomal Dominant, AR for Autosomal Recessive. Lack of inheritance means that it is not confirmed.
The existence of a small number of family reports, with early-onset and exuberant phenotypes, in which the genetic cause was not identified and most of the times was not even investigated, raises the possibility that there are some cases of monogenic DISH and OPLL. There are possibly three main types of OSL: A sporadic form, a type that is secondary to associated metabolic disorders and a hereditary type. It is now clear that most OSL cases do not follow a simple, single gene Mendelian inheritance pattern, but instead are multifactorial disorders developing in individuals with a genetic predisposition from a variety of genetic variants in different genes.
The existence of spontaneous and manipulated animal models for both DISH and OPLL could facilitate the identification of causal human genetic factors. It seems probable that the human phenotype of OPLL and DISH are likely to be caused by mutations in genes that underlie the animal models for these disorders. As far as we know, there are no reports of SLC29A1 (ENT1 mice model for DISH) human gene mutations in association with DISH. The association of ENPP1 with OPLL susceptibility (31, 47–49) is still unsubstantiated (50). Interestingly, in one study the authors found that the combination of variants in ENPP1 and LEPR genes was associated with the location and extension of OPLL (51). An interesting report about hypophosphatemic rickets in an OPLL patient due to a homozygous mutation in the ENPP1 gene (53), substantiates the likely importance of this gene in the etiopathogenic mechanism of OSL.
The case of the ank mouse has been quite different. In humans, analysis in the ANKH gene has identified several mutations that segregate with CC phenotype but only in a very limited subset of pedigrees. The co-coexistence of spinal ossification with CC is well supported in the literature (10, 12, 13), indicating a strong genetic link between these disorders. The genetic confirmation between spinal ossification and CC comes from two animal models—twy and ankh mice—the mouse models for OPLL and CC, develop spinal ossification and hydroxyapatite arthropathy. Both genes, ENPP1 and ANKH, regulate PPi levels thus having an essential role in bone mineralization and soft tissue calcification. The association of ENPP1 variants with Chondrocalcinosis, is considered a minor determinant of the disease (58, 59).
Three different genetic variants in COL6A1 have been associated with both DISH and OPLL. Results from these studies are inconsistent due to the type of variant associated, the lack of explanation of the pathogenic mechanism and the low numbers of individuals studied. Further progress in investigation of DISH requires a concerted approach, similar to the ones used to target the genetic basis of OPLL. In the latter case linkage studies, candidate gene association studies and even genome wide association studies were performed and revealed that OPLL is genetically heterogenous. Despite all the studies, and the large number of genes that have been associated with OSL, most of the associations are still inconsistent because genetic variants were localized in non-coding regions. Several genes involved many potential low risk effects in OSL inheritance, so there is insufficient power and analysis for their detection.
The higher prevalence of OSL in patients with endocrine, nutritional and metabolic disorders made us wonder if the known genetic cause for these associated disorders could help to clarify the putative genetic pathways involved in the etiology of OSL. The ectopic calcification occurring is most probably predisposed by the balance between the expression of specific genes that act directly or indirectly on the phosphorus to calcium ratio. The crucial role of angiogenesis in DISH etiology has also been suggested, as it might be the common pathogenic background of some conditions included in metabolic syndrome. Nonetheless, there are several case reports of patients with monogenic metabolic disorders with the occurrence of DISH and OPLL.
A validated set of classification criteria for diseases characterized by ectopic mineralization of spinal tissues is of utmost importance for genetic studies so homogeneous phenotype groups can be established for investigation. This is particularly important in DISH because this disease is characterized by the ossification of the anterior spinal ligaments and generalized symmetrical enthesopathic calcifications, which may well be among the first manifestations of the disease or the main evidence of the disease in a subset of patients. At this time, DISH disease is requiring a validated set of criteria to robustly describe and establish homogeneous cohorts of patients. A more comprehensive designation of DISH, including patients with early phase disease, are clearly indispensable for genetic studies (Mader et al., 2013). On the other hand, great advances have been made in understanding the presentation of different types of OPLL.
Taken together the collected evidence suggests OSL has a heterogeneous genetic basis. The rapid advance in methods for genetic studies has brought new and interesting insights into ectopic calcification, and is providing confirmation about the importance of genes for the regulation of Pi/PPi levels, which control mineralization. Future genome-scale approaches will contribute to pinpoint susceptibility genes. However, to provide sufficient analytical power, the number of patients needs to be enlarged and the clinical/radiological disease classification, especially in DISH patients, needs substantial improvement. International collaborations are essential to increase sample size and overcome analytical challenges caused by the genetic heterogeneity of these complex diseases of calcification.
BP and AC wrote the manuscript; all the authors provided critical revision and contributed to the final version of the manuscript.
The present publication was funded by Fundação Ciência e Tecnologia, IP national support through CHRC (UIDP/04923/2020).
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Keywords: ossification, genetics, ectopic calcification, diffuse idiopathic skeletal hyperostosis, ossification of posterior longitudinal ligament
Citation: Couto AR, Parreira B, Power DM, Pinheiro L, Madruga Dias J, Novofastovski I, Eshed I, Sarzi-Puttini P, Pappone N, Atzeni F, Verlaan J-J, Kuperus J, Bieber A, Ambrosino P, Kiefer D, Khan MA, Mader R, Baraliakos X and Bruges-Armas J (2022) Evidence for a genetic contribution to the ossification of spinal ligaments in Ossification of Posterior Longitudinal Ligament and Diffuse idiopathic skeletal hyperostosis: A narrative review. Front. Genet. 13:987867. doi: 10.3389/fgene.2022.987867
Received: 06 July 2022; Accepted: 16 September 2022;
Published: 07 October 2022.
Edited by:
Jordi Pérez-Tur, Institute of Biomedicine of Valencia (CSIC), SpainReviewed by:
Michael G. Fehlings, Toronto Western Hospital, CanadaCopyright © 2022 Couto, Parreira, Power, Pinheiro, Madruga Dias, Novofastovski, Eshed, Sarzi-Puttini, Pappone, Atzeni, Verlaan, Kuperus, Bieber, Ambrosino, Kiefer, Khan, Mader, Baraliakos and Bruges-Armas. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jácome Bruges-Armas, YnJ1Z2VzYXJtYXNAZ21haWwuY29t
†These authors have contributed equally to this work
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