Nemours/Alfred I. duPont Hospital for Children, Wilmington, DE, United States.
Medical Genetics Service, HCPA, Dep. Genetics, UFRGS, INAGEMP, Porto Alegre, Brazil.
Mol Genet Metab. 2018 Sep;125(1-2):44-52. doi: 10.1016/j.ymgme.2018.04.011. Epub 2018 May 17.
To explore the correlation between glycosaminoglycan (GAG) levels and mucopolysaccharidosis (MPS) type, we have evaluated the GAG levels in blood of MPS II, III, IVA, and IVB and urine of MPS IVA, IVB, and VI by tandem mass spectrometry. Dermatan sulfate (DS), heparan sulfate (HS), keratan sulfate (KS; mono-sulfated KS, di-sulfated KS), and the ratio of di-sulfated KS in total KS were measured. Patients with untreated MPS II had higher levels of DS and HS in blood while untreated MPS III had higher levels of HS in blood than age-matched controls. Untreated MPS IVA had higher levels of KS in blood and urine than age-matched controls. The ratio of blood di-sulfated KS/total KS in untreated MPS IVA was constant and higher than that in controls for children up to 10 years of age. The ratio of urine di-sulfated KS/total KS in untreated MPS IVA was also higher than that in age-matched controls, but the ratio in untreated MPS IVB was lower than controls. ERT reduced blood DS and HS in MPS II, and urine KS in MPS IVA patients, although GAGs levels remained higher than the observed in age-matched controls. ERT did not change blood KS levels in MPS IVA. MPS VI under ERT still had an elevation of urine DS level compared to age-matched controls. There was a positive correlation between blood and urine KS in untreated MPS IVA patients but not in MPS IVA patients treated with ERT. Blood and urine KS levels were secondarily elevated in MPS II and VI, respectively. Overall, measurement of GAG levels in blood and urine is useful for diagnosis of MPS, while urine KS is not a useful biomarker for monitoring therapeutic efficacy in MPS IVA.
为了探讨糖胺聚糖(GAG)水平与黏多糖贮积症(MPS)类型之间的相关性,我们通过串联质谱法评估了 MPS II、III、IVA 和 IVB 患者的血液以及 MPS IVA、IVB 和 VI 患者的尿液中的 GAG 水平。我们测量了硫酸皮肤素(DS)、硫酸乙酰肝素(HS)、硫酸角质素(KS;单硫酸化 KS、双硫酸化 KS)以及双硫酸化 KS 与总 KS 的比值。未治疗的 MPS II 患者的血液 DS 和 HS 水平较高,而未治疗的 MPS III 患者的血液 HS 水平较年龄匹配的对照组高。未治疗的 MPS IVA 患者的血液和尿液中的 KS 水平高于年龄匹配的对照组。未治疗的 MPS IVA 患者的血液中二硫酸化 KS 与总 KS 的比值保持不变,且高于年龄匹配的对照组的儿童患者。未治疗的 MPS IVA 患者的尿液中二硫酸化 KS 与总 KS 的比值也高于年龄匹配的对照组,但未治疗的 MPS IVB 患者的比值低于对照组。ERT 降低了 MPS II 患者的血液 DS 和 HS,以及 MPS IVA 患者的尿液 KS,但 GAG 水平仍高于年龄匹配的对照组。ERT 未改变 MPS IVA 患者的血液 KS 水平。接受 ERT 的 MPS VI 患者的尿液 DS 水平仍高于年龄匹配的对照组。未治疗的 MPS IVA 患者的血液和尿液 KS 之间存在正相关,但接受 ERT 的 MPS IVA 患者之间无此相关性。未治疗的 MPS IVA 患者的血液和尿液 KS 水平分别升高。总的来说,血液和尿液 GAG 水平的测量有助于 MPS 的诊断,而尿液 KS 不是监测 MPS IVA 治疗效果的有用生物标志物。
Mol Genet Metab. 2018-5-17
Mol Genet Genomic Med. 2018-11
Mol Genet Metab. 2013-6-21
Mol Genet Metab Rep. 2019-2-5
Mol Genet Metab. 2010-9-17
Mol Ther Methods Clin Dev. 2025-7-30
Int J Mol Sci. 2025-5-21
Int J Mol Sci. 2025-5-2
Mol Ther Methods Clin Dev. 2025-3-14
Ital J Pediatr. 2024-10-8
J Inherit Metab Dis. 2018-3-19
Mol Genet Metab. 2017-12-13
Mol Genet Metab. 2017
Nihon Masu Sukuriningu Gakkai Shi. 2014
Mol Genet Metab. 2015-2