Literature DB >> 24843807

Diffuse idiopathic skeletal hyperostosis: A review.

Fábio A Nascimento1, Luana Antunes Maranha Gatto2, Roberto Oliver Lages3, Heraldo Mello Neto4, Zeferino Demartini5, Gelson Luis Koppe6.   

Abstract

BACKGROUND: Diffuse idiopathic skeletal hyperostosis (DISH) is a systemic noninflammatory disease characterized by ossification of the entheses.
METHODS: This paper reviews the etiopathogenesis, epidemiology, clinical features, differential diagnosis, and treatment of DISH, based on current available literature.
RESULTS: Exact prevalence and incidence of DISH remains undetermined. Many external and genetic factors have been reported as being contributors to the pathogenesis of DISH. Current theories focus on the pathologic calcification of the anterior longitudinal ligament of the spine as the main physiopathological mechanism of disease. Clinical features are variable from monoarticular sinovitis to airway obstruction, and can be associated to systemic conditions. Comorbidities include obesity, hypertension, diabetes mellitus, hyperinsulinemia, dyslipidemia, and hyperuricemia according to a number of reports.
CONCLUSIONS: DISH is a disease which involves the calcification of the anterior longitudinal ligament of the spine and can be associated with numerous clinical presentations and comorbidities.

Entities:  

Keywords:  Anterior Longitudinal Ligament; Forestier's disease; diffuse idiopathic skeletal hyperostosis

Year:  2014        PMID: 24843807      PMCID: PMC4023007          DOI: 10.4103/2152-7806.130675

Source DB:  PubMed          Journal:  Surg Neurol Int        ISSN: 2152-7806


INTRODUCTION

Forestier's disease was first described by Jacques Forestier and his student Jaume Rotes-Querol in 1950 under the name “senile ankylosing vertebral hyperostosis”.[8] However, it is now known that this disease is neither limited to the spine nor to older subjects. In 1976, Resnick and Niwayama coined the term “diffuse idiopathic skeletal hyperostosis” (DISH), which is currently widely utilized. Independently of how this condition is named, it consists in a systemic noninflammatory disease characterized by ossification of the entheses – the bony attachment of tendons, ligaments, and joint capsules.[17]

ETIOPATHOGENESIS

While the cause of DISH remains unclear, mechanical factors (such as the location of the aorta contributing to the development of bony bridging on specific sites), genetic factors (HLA genes), environmental exposures (fluoride, vitamin A/retinol), drugs (isotretinoin, etretinate, acitretin and other vitamin A derivatives), and metabolic conditions have been hypothesized to be relevant [Table 3].[457151921]
Table 3

Etiopathogenesis of DISH

Criteria to diagnose diffuse idiopathic skeletal hyperostosis according to Resnick and Niwayama Epidemiology of DISH-it increases in older males: Variable factors Etiopathogenesis of DISH Although many external and genetic factors have been reported as being contributors of the pathogenesis of DISH, most of the current theories focus on the pathologic calcification of the anterior longitudinal ligament of the spine. The majority of these theories postulate that this process is due to the abnormal growth and function of the osteoblasts in the osteoligamentary binding.[2] However, it is important to clarify that not all authors accept the association between pathologic calcification and increased bone mineral density.[6]

EPIDEMIOLOGY

In terms of epidemiology of DISH, it varies in numerous reports – the absence of a consensus about the exact definition of the disease certainly contributes to not being able to determine its exact epidemiology. However, there are a few well-designed studies that try to estimate its prevalence. Holton et al. assessed 298 men aged older than 65 years from the general population. It was found that the prevalence of this disease (using Resnick's definition) in this age group was 42%.[9] Another study from the 1990s postulates that its prevalence is higher than 10% in patients over 70 years.[3] Furthermore, Weinfeld analyzed the data from two large American Midwest metropolitan hospital populations. It was concluded that the prevalence of DISH in this Anglo-Saxon population over 50 years of age is 25% in males and 15% in females. At 70 years of age, there is a 35% and 26% increase in prevalence, respectively.[22] Although the exact prevalence and incidence remains undetermined, it is well known that DISH is more frequent in men, and the incidence increases with age [Table 2] – mainly affecting patients over the age of 40 years.
Table 2

Epidemiology of DISH-it increases in older males: Variable factors

CLINICAL FEATURES

Various signs and symptoms have been described in patients suffering from DISH, such as polyarticular pain, neck/thoracic/lumbar/extremity pain, acute monoarticular sinovitis, limited range of spinal motion, dysphagia, increased susceptibility to unstable spinal fractures, and different degrees of airway obstruction [Table 5].[23] The frequency and quality of complaints among these subjects varies by the site of the pathologic ossification. In contrast, many individuals who are diagnosed with DISH (visible ossifications on imaging studies acquired for other medical reasons) may be completely asymptomatic. Although DISH affects selectively the spine (with predilection to its thoracic portion – the hallmark of the disease is considered to be the ossification of the anterolateral aspect of the thoracic spine) [Figures 1–3], it is important to emphasize that this condition is not limited to the spine and has often been reported to involve multiple peripheral locations as well (extraspinal entheseal ossfications). These include periarticular hyperostosis of the hands, pelvis, knees, elbows, etc., The enthesophytes seen in DISH must be differentiated from osteophytes due to osteoarthritis and from syndesmophytes due to spondyloarthritis [Table 4]. Some of the features that help differentiate DISH from other pathologic structures are: Developing from joints that are rarely affected by osteoarthritis, such as shoulder, elbow, and metacarpophalangeal joints; developing from bone that is distant from the bone–cartilage junction; affecting distinctive entheses such as the calcaneal spur, quadriceps tendon, among others.[1213]
Table 5

Clinical features of DISH

Figure 1

Sagittal cervical CT scan – Bone window

Figure 3

Same CT scan in 3D reconstruction

Table 4

Pathologic calcification of DISH

Sagittal cervical CT scan – Bone window CT scan from the same patient demonstrating hyperostosis and anterior cervical fusion Same CT scan in 3D reconstruction Pathologic calcification of DISH Clinical features of DISH The most commonly used classification criteria were defined by Resnick and Niwayama and required following anterolateral ossifications of at least four contiguous thoracic vertebral segments, preservation of the intervertebral disk spaces, and absence of apophyseal joint degeneration or sacroiliac inflammatory changes [Table 1].[16]
Table 1

Criteria to diagnose diffuse idiopathic skeletal hyperostosis according to Resnick and Niwayama

Despite the fact that the presence of constitutional and metabolic abnormalities is not mandatory for making a formal diagnosis of DISH, it is known that systemic conditions are associated with DISH in varying degrees. These comorbidities include obesity, hypertension, diabetes mellitus, hyperinsulinemia, dyslipidemia, and hyperuricemia, according to a number of reports.[101218] Additionally, two recent studies showed that these patients have a higher incidence of risk factors for stroke, higher prevalence of metabolic syndrome, and a higher risk for future coronary events.[1114]

DIFFERENTIAL DIAGNOSIS

The most common conditions that may also present with bony excrescences, similar to those related to DISH, are Spondylosis Deformans and Ankylosing Spondylitis. The former disease is by far the most common of the disorders to be considered in the differential diagnosis of DISH. Spondylosis Deformans, however, does not affect the anterior longitudinal ligament in the thoracic spine, and that is how one can differentiate these two conditions. The latter disease shares some features seen with DISH, such as a preponderance in males and an association with ligamentous ossification and syndesmophytes. One may distinct these two conditions by noting that in Ankylosing Spondylitis, the bony bridges are slender, vertical, and involve the outer margin of the annulus fibrosus and do not involve the anterior longitudinal ligament. In addition, erosions and bony ankylosis of the sacroiliac and apophyseal joints are not seen in DISH.

TREATMENT

Therapy for DISH is based on symptomatic and empiric treatment. There have been no well-designed studies evaluating the effectiveness of any therapy in this disease. In general, physical therapy, analgesics, sedation, antiinflammatory drugs, and muscle relaxants, associated with appropriate diet, have all been successful in managing the majority of patients with DISH.[120] Even though few articles until now have focused on indications for surgery, it is generally accepted that surgery is indicated for patients with severe symptoms (such as airway obstruction and/or dysphagia) in whom conservative approach has failed.
  22 in total

Review 1.  Calcium deposition and associated chronic diseases (atherosclerosis, diffuse idiopathic skeletal hyperostosis, and others).

Authors:  Fabiola Atzeni; Piercarlo Sarzi-Puttini; Maorizio Bevilacqua
Journal:  Rheum Dis Clin North Am       Date:  2006-05       Impact factor: 2.670

2.  Senile ankylosing hyperostosis of the spine.

Authors:  J FORESTIER; J ROTES-QUEROL
Journal:  Ann Rheum Dis       Date:  1950-12       Impact factor: 19.103

3.  Radiographic and pathologic features of spinal involvement in diffuse idiopathic skeletal hyperostosis (DISH).

Authors:  D Resnick; G Niwayama
Journal:  Radiology       Date:  1976-06       Impact factor: 11.105

4.  Extraspinal tendon and ligament calcification associated with long-term therapy with etretinate.

Authors:  J J DiGiovanna; R K Helfgott; L H Gerber; G L Peck
Journal:  N Engl J Med       Date:  1986-11-06       Impact factor: 91.245

5.  Patients with diffuse idiopathic skeletal hyperostosis do not have increased peripheral bone mineral density and geometry.

Authors:  Prisca Eser; Harald Bonel; Michael Seitz; Peter M Villiger; Daniel Aeberli
Journal:  Rheumatology (Oxford)       Date:  2010-02-15       Impact factor: 7.580

6.  The role of growth factors in degenerative joint disorders.

Authors:  R W Moskowitz; B Boja; C W Denko
Journal:  J Rheumatol Suppl       Date:  1991-02

Review 7.  New developments in our understanding of DISH (diffuse idiopathic skeletal hyperostosis).

Authors:  Piercarlo Sarzi-Puttini; Fabiola Atzeni
Journal:  Curr Opin Rheumatol       Date:  2004-05       Impact factor: 5.006

8.  [Forestier disease and metabolism disorders. A prospective controlled study of 25 cases].

Authors:  N Troillet; J C Gerster
Journal:  Rev Rhum Ed Fr       Date:  1993-04

9.  Cervical spondylosis and dysphagia.

Authors:  B C Umerah; B K Mukherjee; O Ibekwe
Journal:  J Laryngol Otol       Date:  1981-11       Impact factor: 1.469

Review 10.  Diffuse idiopathic skeletal hyperostosis (Forestier-Rotes-Querol disease): what's new?

Authors:  Bernard Mazières
Journal:  Joint Bone Spine       Date:  2013-04-06       Impact factor: 4.929

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  17 in total

1.  Diffuse idiopathic skeletal hyperostosis with cervical myelopathy.

Authors:  Aria Nouri; Michael G Fehlings
Journal:  CMAJ       Date:  2017-03-13       Impact factor: 8.262

2.  Subjects with diffuse idiopathic skeletal hyperostosis have an increased burden of coronary artery disease: An evaluation in the COPDGene cohort.

Authors:  Sytse F Oudkerk; Firdaus A A Mohamed Hoesein; Willem PThM Mali; F Cumhur Öner; Jorrit-Jan Verlaan; Pim A de Jong; Gregory L Kinney; John Hokanson; David Lynch; Edwin K Silverman; Matthew J Budoff; Elizabeth A Regan
Journal:  Atherosclerosis       Date:  2019-05-30       Impact factor: 5.162

3.  Diffuse idiopathic skeletal hyperostosis and isotretinoin in cystic acne.

Authors:  Sizheng Zhao; Nicola J Goodson
Journal:  BMJ Case Rep       Date:  2015-06-23

4.  Diffuse idiopathic skeletal hyperostosis (DISH) of the elbow: a controlled radiological study.

Authors:  Christine Beyeler; Sergio R Thomann; Niklaus J Gerber; Christine Kunze; Daniel Aeberli
Journal:  BMC Musculoskelet Disord       Date:  2015-05-16       Impact factor: 2.362

5.  Prevalence of Diffuse Idiopathic Skeletal Hyperostosis in Patients with Spinal Disorders.

Authors:  Hiromitsu Toyoda; Hidetomi Terai; Kentaro Yamada; Akinobu Suzuki; Sho Dohzono; Tomiya Matsumoto; Hiroaki Nakamura
Journal:  Asian Spine J       Date:  2017-02-17

6.  Surgical treatment of diffuse idiopathic skeletal hyperostosis of cervical spine with dysphagia - Case report.

Authors:  Mikołaj Dąbrowski; Adam Sulewski; Jacek Kaczmarczyk; Łukasz Kubaszewski
Journal:  Ann Med Surg (Lond)       Date:  2020-07-14

7.  Prevalence of diffuse idiopathic skeletal hyperostosis among elderly subjects referred for radiological investigation in tertiary hospital at Oman.

Authors:  Srinivasa Rao Sirasanagandla; Humoud Al Dhuhli; Ahmed Al Abri; Ahmed Salmi; Sathish Kumar Jayapal; Crosetto Sara; Sanjay Jaju
Journal:  Anat Cell Biol       Date:  2018-09-28

8.  Anterior longitudinal ligament in diffuse idiopathic skeletal hyperostosis: Ossified or displaced?

Authors:  Jonneke S Kuperus; Esther J M Smit; Behdad Pouran; Robbert W van Hamersvelt; Marijn van Stralen; Peter R Seevinck; Constantinus F Buckens; Ronald L A W Bleys; Harrie H Weinans; F Cumhur Oner; Pim A de Jong; Jorrit-Jan Verlaan
Journal:  J Orthop Res       Date:  2018-05-24       Impact factor: 3.494

9.  Total knee arthroplasty in a case of diffuse idiopathic skeletal hyperostosis; challenges in ligament balancing and deformity correction.

Authors:  Anoop Jhurani; Piyush Agarwal; Mukesh Aswal; Vishal Gupta
Journal:  J Orthop Case Rep       Date:  2019

10.  Severe hip joint motion restriction in a patient with diffuse idiopathic skeletal hyperostosis: A case report.

Authors:  Wonho Lee; Wook Ro Kim; Min Cheol Chang
Journal:  Medicine (Baltimore)       Date:  2018-05       Impact factor: 1.889

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