Spinal manifestations of DISH consist of craniocaudally oriented paravertebral and paradiscal bone JAK inhibitor formation and osteophytes with a predilection for the anterior longitudinal ligament. Spinal ossifications can be extensive and may lead to esophageal stenosis or neurological disorders. Controversy exists about the implications of vertebral ossifications for the mechanical stability of the spine. It has been suggested that the fused segments are more prone to fracture
even after minimal trauma [6]. On the other hand, different studies have shown consistently higher bone mineral density (BMD) in patients with hyperostosis, implying a lower fracture risk [7–9]. All of these previous studies were performed with dual energy X-ray absorptiometry (DXA), which measures two-dimensional areal BMD as a sum of all attenuating tissues in the beam projection. Flowing ossifications may lead to overestimation of BMD values by DXA, limiting evaluation of fracture risk in these patients. It is not clear what BMD to expect in trabecular bone when measurement is performed using quantitative computed tomography (QCT), which allows separate measurement of trabecular bone and cortical bone of the spine in three dimensions, not 4SC-202 molecular weight influenced by surrounding osteophytes. Knowledge of fragility fractures
and BMD in association with DISH is limited. The goals of this study were to evaluate the prevalence selleck inhibitor of DISH in association with presence and absence of vertebral fractures and to analyze BMD determined by DXA and QCT in relation to vertebral DISH and fractures. Materials and method Study participants A total of 342 participants were randomly selected from 5,995 men 65 years or older participating in the prospective multicenter, observational Osteoporotic Fractures in Men (MrOS)
Study; details of MrOS have been published previously [10, 11]. The baseline examinations were performed 4-Aminobutyrate aminotransferase from March 2000 to April 2002 at six clinical centers in the United States: Birmingham, AL; Minneapolis, MN; Palo Alto, CA; Pittsburgh, PA; Portland, OR; and San Diego, CA. Briefly, the inclusion criteria included: (1) ability to walk, (2) absence of bilateral hip replacement, (3) ability to provide self-reported data, (4) residence near a clinical site for the duration of the study, (5) absence of a medical condition that would result in imminent death, and (6) ability to understand and sign an informed consent. The protocol and consent forms for MrOS were approved by the institutional review boards at each of the participating institutions. All participants provided written informed consent. Imaging and image analysis Lateral radiographs of the thoracic and lumbar spine were available in all 342 participants at baseline. Thoracic radiographs were centered at T7 and lumbar radiographs at L3.