Département de rhumatologie, université de Lille, 59000 Lille, France; PMOI, EA 4490, 59000 Lille, France.
Division de rhumatologie, département de médecine, CHU de Québec, université Laval, Québec, G1V4G2 QC, Canada.
Joint Bone Spine. 2018 Dec;85(6):693-699. doi: 10.1016/j.jbspin.2018.01.007. Epub 2018 Mar 2.
A finding of high bone mineral density (BMD) from routine dual-energy X-ray absorptiometry (DXA) screening is not uncommon. No consensus exists about the definition of high BMD, and T-score and/or Z-score cutoffs of ≥+2.5 or ≥+4 have been suggested. The many disorders that can result in high BMD are usually classified based on whether the BMD changes are focal vs. generalized or acquired vs. constitutional. In over half the cases, careful interpretation of the DXA report and images identifies the cause as an artefact (e.g., degenerative spinal disease, vascular calcifications, or syndesmophytes) or focal lesion (e.g., sclerotic bone metastasis or Paget's disease). Generalized acquired high BMD may be secondary to a diverse range of disorders such as fluorosis, diffuse bone sclerosis related to renal osteodystrophy, hematological diseases, and hepatitis C. Identification of the cause may require additional investigations such as imaging studies, serum tryptase assay, or serological tests for the hepatitis C virus. Finally, high BMD is a feature of many genetic diseases, most notably osteopetrosis and the disorders caused by mutations in the sclerostin gene SOST (sclerosing bone dysplasia and van Buchem disease) or in the LRP5 gene encoding the low-density lipoprotein receptor-related protein 5 (which is the Wnt co-receptor).
从常规双能 X 射线吸收法(DXA)筛查中发现高骨密度(BMD)并不罕见。目前尚不存在关于高 BMD 的定义共识,有人建议使用 T 评分和/或 Z 评分截断值≥+2.5 或≥+4。许多可导致高 BMD 的疾病通常基于 BMD 变化是局灶性与全身性、获得性与遗传性进行分类。在一半以上的情况下,仔细解读 DXA 报告和图像可识别出病因是人为因素(例如,退行性脊柱疾病、血管钙化或骨桥)或局灶性病变(例如,硬化性骨转移或 Pagets 病)。获得性全身性高 BMD 可能继发于多种疾病,如氟中毒、与肾性骨营养不良相关的弥漫性骨硬化、血液系统疾病和丙型肝炎。确定病因可能需要进一步检查,如影像学研究、血清胰蛋白酶检测或丙型肝炎病毒血清学检查。最后,许多遗传性疾病都有高 BMD 的特征,最常见的是骨硬化症和由 Sost 基因(SOST)突变引起的疾病(硬化性骨发育不良和范可尼骨发育不良)或低密度脂蛋白受体相关蛋白 5(LRP5)基因突变引起的疾病(编码 Wnt 共受体)。