用双能x线吸收测量法评估法布里病的骨质减少和骨质疏松。

IF 3.4 2区 医学 Q2 GENETICS & HEREDITY
Alyaa Shmara, Grace Lee, Mania Mgdsyan, Kathy Hall, Nadia Sadri, Angela Martin-Rios, Kelsey Valentine, Tatiana Kain, Madeleine Pahl, Lynda E Polgreen, Virginia Kimonis
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引用次数: 0

摘要

背景:法布里病(FD)是一种罕见的多系统溶酶体积存病,主要影响心脏和肾脏。FD的一个不被重视的表现是骨密度降低。目前,对于FD患者的常规骨密度评估以及骨质疏松和骨质减少的治疗尚无具体的指南。材料和方法:为了确定FD中低骨密度的频率,我们研究了双能x线吸收仪(DXA)扫描结果,该扫描结果是2008-2023年期间在加州大学欧文分校医学中心随访的25名个体的常规护理的一部分。收集了12名男性和13名女性腰椎和股骨颈的最新骨密度结果,以检查低骨密度的患病率。选择腰椎或股骨颈Z-和/或t -评分最低的患者进行分析。与DXA扫描结果同时(±9个月内)收集人口统计学因素、疾病和ERT状态以及其他实验室值,并使用Z-和t评分进行分析以评估相关性。在我们的队列中,平均年龄为51岁(中位数为56岁,范围为18-77岁)。对所有参与者的z -评分和绝经后女性和≥50岁男性的t -评分进行分析,并将其与疾病持续时间、BMI、肾功能(由eGFR测量)、血浆GL3、Lyso-GL3、钙、维生素D和碱性磷酸酶水平等各项指标相关联。这些参数与DXA扫描结果同步。结果:所有参与者的平均z分数为-1.2±1.3(范围为-4.6至1.6)。24%的参与者(n = 6)的z分数显著低于-2.0。结论:该队列的研究结果突出了FD中低骨密度的高患病率,以及低Z和T评分与Lyso-GL3水平升高和低钙水平之间的相关性。我们没有发现肾功能和维生素D水平的相关性。我们讨论法布里病骨质减少/骨质疏松的病因、预防和治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing osteopenia and osteoporosis with dual-energy x-ray absorptiometry studies in Fabry disease.

Background: Fabry disease (FD) is a rare multi-systemic lysosomal storage disease that affects the heart and kidneys most significantly. An underappreciated manifestation of FD is reduced bone mineral density. Currently, there are no specific guidelines for routine bone density assessments, and treatment of osteoporosis and osteopenia in FD.

Materials and methods: To ascertain the frequency of low bone mineral density in FD we studied dual-energy x-ray absorptiometry (DXA) scans obtained as part of routine care from a cohort of 25 individuals followed at the University of California-Irvine Medical Center for the period 2008-2023. The most recent BMD results for the lumbar spine and femoral neck were collected from 12 males and 13 females to examine the prevalence of low bone mineral density. The lowest Z- and/or T-scores of either lumbar spine or femoral neck were selected for analysis. Demographic factors, disease and ERT status, and other laboratory values were collected concurrently (within ± 9 months) with DXA scan results and were analyzed with Z- and T-scores to assess for correlations. In our cohort the mean age was 51 years (median 56 years, range 18-77 years). The Z-scores for all participants and T-scores from postmenopausal women and men ≥ 50-year-old were analyzed and correlated with various measures including disease duration, BMI, renal function (measured by eGFR), plasma GL3, Lyso-GL3, calcium, vitamin D, and alkaline phosphatase levels. These parameters were concurrent with DXA scan results.

Results: The average Z-score for all the participants was -1.2 ± 1.3 (range -4.6 to 1.6). Twenty-four percent of all participants (n = 6) had significantly low Z-scores ≤ -2.0. To identify the frequency of subjects with osteopenia, defined as T-score between -1.0 and -2.5 and osteoporosis defined as T-score < -2.5, T-scores were analyzed in postmenopausal women (n = 8) and men 50 years and older (n = 7). Of these 15 individuals, average T-score was -2.2 ± 1.3 (range -5.4 to 0.3), and 86.7% (n = 13) had abnormal results (osteopenia and osteoporosis), 53.3% (n = 8) had osteoporosis and 33.3% (n = 5) had osteoporosis. We found a significant difference in Z-scores between male (-1.98 ± 1.33) and female patients (-.45 ± 0.82) t (23) = 3.487 (p =  < 0.001). We did not find any differences in z-scores between different ethnic backgrounds. There was a strong negative correlation between Z-scores and Lyso-GL3 levels [r (15) = -.72, p = .001] and a moderate positive correlation between Z-scores and body mass index (BMI) [r (23) = .43, p = .033]. No correlation was found between Z-scores and calcium levels. There is a strong negative correlation between T-scores and Lyso-GL3 levels [r (8) = -.86, p = .001] and a negative correlation between T-scores and participants' ages at the time of DXA [r (13) = -.57, p = 0.028]. There is a positive correlation between T- scores and calcium levels [r (12) = .58, p = 0.030]. No significant correlation was observed between T-scores and BMI. There was no correlation between Z or T- scores and disease duration, duration of ERT use, renal function (measured by eGFR), GL3, creatinine, alkaline phosphatase levels, or their use of vitamin D or concomitant antiepileptic medications.

Conclusion: The findings of this cohort highlight the high prevalence of low bone mineral density in FD and correlations of low Z and T- scores with elevated levels of Lyso-GL3, and low calcium levels. We did not find correlations with renal function, and vitamin D levels. We discuss etiology, prevention, and treatment strategies for osteopenia/osteoporosis in Fabry disease.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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