Pichler Karin, Karall Daniela, Kotzot Dieter, Steichen-Gersdorf Elisabeth, Rümmele-Waibel Alexandra, Mittaz-Crettol Laureane, Wanschitz Julia, Bonafé Luisa, Maurer Kathrin, Superti-Furga Andrea, Scholl-Bürgi Sabine
Clinic for Pediatrics I, Inherited Metabolic Disorders, Medical University of Innsbruck, Anichstrasse 35, A-6020 Innsbruck, Austria.
Department of Pediatrics, Division of Neonatology, Pediatric Intensive Care and Neuropediatrics, Medical University of Vienna, Waehringer Guertel 18-20, A-1090 Vienna, Austria.
Sci Rep. 2016 Sep 30;6:34017. doi: 10.1038/srep34017.
Multicentric osteolysis, nodulosis and arthropathy (MONA) spectrum disorder is a rare inherited progressive skeletal disorder caused by mutations in the matrix metalloproteinase 2 (MMP2) gene. Treatment options are limited. Herein we present successful bisphosphonate therapy in three affected patients. Patients were treated with bisphosphonates (either pamidronate or zoledronate) for different time periods. The following outcome variables were assessed: skeletal pain, range of motion, bone densitometry, internal medical problems as well as neurocognitive function. Skeletal pain was dramatically reduced in all patients soon after initiation of therapy and bone mineral density increased. Range of motion did not significantly improve. One patient is still able to walk with aids at the age of 14 years. Neurocognitive development was normal in all patients. Bisphosphonate therapy was effective especially in controlling skeletal pain in MONA spectrum disorder. Early initiation of treatment seems to be particularly important in order to achieve the best possible outcome.
多中心骨质溶解、结节病和关节病(MONA)谱系障碍是一种罕见的遗传性进行性骨骼疾病,由基质金属蛋白酶2(MMP2)基因突变引起。治疗选择有限。在此,我们报告了三例受累患者接受双膦酸盐治疗成功的案例。患者接受了不同时间段的双膦酸盐(帕米膦酸盐或唑来膦酸盐)治疗。评估了以下结果变量:骨骼疼痛、活动范围、骨密度测定、内科问题以及神经认知功能。治疗开始后不久,所有患者的骨骼疼痛均显著减轻,骨密度增加。活动范围没有显著改善。一名患者在14岁时仍需借助辅助器具行走。所有患者的神经认知发育均正常。双膦酸盐治疗在控制MONA谱系障碍的骨骼疼痛方面尤其有效。为了获得最佳结果,早期开始治疗似乎尤为重要。