Longitudinal course of circulating miRNAs in a patient with hypophosphatasia and asfotase alfa treatment: a case report

被引:1
作者
Hadzimuratovic, Benjamin [1 ,2 ,3 ]
Haschka, Judith [1 ,2 ,3 ]
Hackl, Matthias [4 ]
Diendorfer, Andreas B. [4 ]
Mittelbach, Andreas [5 ]
Feurstein, Julia [1 ,2 ,3 ]
Zwerina, Jochen [1 ,2 ,3 ]
Resch, Heinrich [6 ,7 ]
Kocijan, Roland [1 ,2 ,3 ,7 ]
机构
[1] Hanusch Hosp, Ludwig Boltzmann Inst Osteol Hanusch Hosp OEGK, Med Dept 1, A-1140 Vienna, Austria
[2] Hanusch Hosp, AUVA Trauma Ctr Meidling, A-1140 Vienna, Austria
[3] Hanusch Hosp, Med Dept 1, A-1140 Vienna, Austria
[4] TAmiRNA GmbH, A-1110 Vienna, Austria
[5] Hanusch Hosp, Inst Phys Med & Rehabil, A-1140 Vienna, Austria
[6] St Vincent Hosp, Dept Internal Med 2, VINFORCE, A-1060 Vienna, Austria
[7] Sigmund Freud Univ, Med Fac Bone Dis, A-1020 Vienna, Austria
关键词
hypophosphatasia; HPP; micro-RNAs; miRNAs; ALP; asfotase alfa; enzyme replacement therapy; ERT; MICRORNAS; PAIN;
D O I
10.1093/jbmrpl/ziae107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hypophosphatasia (HPP) is characterized by low activity of tissue nonspecific alkaline phosphatase (TNSALP). The enzyme replacement therapy asfotase alfa has been approved for childhood-onset forms of HPP. MicroRNAs (miRNAs) have emerged as a novel disease biomarker, with potential application in therapy monitoring. Circulating miRNAs were analyzed at baseline, months 1, 2, 4, and 16 in a 49-yr-old woman with childhood-onset HPP, chronic musculoskeletal pain, and non-traumatic fractures prior to enzyme replacement therapy. Serum RNA was extracted and sequenced using miRNeasy Mini Kit (Qiagen, Germany), RealSeq Biosciences Kit (Santa Cruz, US) together with miND spike-in control kit (TAmiRNA, Austria) and Illumina NovaSeq 6000 SP1 flow cell (San Diego, US). Brief Pain Inventory Severity and Interference scores (BPI-S/BPI-I), fatigue severity scale (FSS), Patient Global Impression of Improvement (PGI-I), Western Ontario and McMaster university hip disability and osteoarthritis outcome score (WOMAC), fibromyalgia impact questionnaire (FIQ), 6-Minute Walking Test (6-MWT), chair-rise-test (CRT), and handgrip dynamometry (HD) were performed at baseline and different timepoints during the therapy. Out of >800 screened, 84 miRNAs were selected based on differences in expression profiles between 24 HPP patients and 24 healthy controls. Six miRNAs showed a clear graphic trend and were up- or downregulated by >= 50% reads per million (rpm). These included hsa-let-7i-5p (+50%), hsa-miR-1-3p (-66.66%), hsa-miR-1294 (+63.63%), hsa-miR-206 (-85.57%), hsa-miR-375-3p (-71.43%), and hsa-miR-624-5p (+69.44%). hsa-miR-1-3p and hsa-miR-206 were identified as muscle-specific miRNAs. hsa-mir-375-3p, which negatively regulates osteogenesis, was significantly downregulated. In terms of patient-reported outcomes, BPI-S, BPI-I, FSS, PGI-I, WOMAC, and FIQ showed a reduction by -58.62%, -68.29%, -33.33%, -75.00%, -63.29%, and -43.02%, respectively. 6-MWT improved by +33.89% and CRT by -44.46%. Mean hand grip strength of the right/left hand measured by HD improved by +12.50% and + 23.53%, respectively. miRNA profile changes during the therapy with asfotase alfa, accompanying improvements in functionality tests and quality of life scores.
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页数:11
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