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本文引用的文献

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Gender differences in the prevalence and severity of bone disease in thalassaemia.地中海贫血症骨病患病率和严重程度的性别差异。
Pediatr Endocrinol Rev. 2008 Oct;6 Suppl 1:116-22.
2
Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations.人脯氨酰二肽酶及脯氨酰二肽酶缺乏症:参与脯氨酸循环的酶的特性及其突变影响概述
Amino Acids. 2008 Nov;35(4):739-52. doi: 10.1007/s00726-008-0055-4. Epub 2008 Mar 14.
3
Prolidase-dependent regulation of collagen biosynthesis.胶原生物合成的脯氨酰肽酶依赖性调节。
Amino Acids. 2008 Nov;35(4):731-8. doi: 10.1007/s00726-008-0051-8. Epub 2008 Mar 5.
4
Serum prolidase activity in postmenopausal osteoporosis.绝经后骨质疏松症患者的血清脯氨酰肽酶活性
Minerva Med. 2007 Dec;98(6):647-51.
5
The role of prolidase activity in the diagnosis of uremic bone disease.脯氨酰二肽酶活性在尿毒症骨病诊断中的作用。
Ren Fail. 2006;28(4):271-4. doi: 10.1080/08860220600577726.
6
Antioxidant status in children with homozygous thalassemia.纯合子地中海贫血患儿的抗氧化状态
Indian Pediatr. 2005 Nov;42(11):1141-5.
7
Pathogenesis of osteoporosis: concepts, conflicts, and prospects.骨质疏松症的发病机制:概念、争议与展望。
J Clin Invest. 2005 Dec;115(12):3318-25. doi: 10.1172/JCI27071.
8
Prolidase deficiency and the biochemical assays used in its diagnosis.脯氨酰肽酶缺乏症及其诊断中使用的生化检测方法。
Anal Biochem. 2006 Feb 15;349(2):165-75. doi: 10.1016/j.ab.2005.10.018. Epub 2005 Oct 27.
9
A new automated colorimetric method for measuring total oxidant status.一种用于测量总氧化剂状态的新型自动比色法。
Clin Biochem. 2005 Dec;38(12):1103-11. doi: 10.1016/j.clinbiochem.2005.08.008. Epub 2005 Oct 7.
10
Beta-thalassemia.β地中海贫血
N Engl J Med. 2005 Sep 15;353(11):1135-46. doi: 10.1056/NEJMra050436.

重型地中海贫血患者的脯肽酶活性和氧化状态。

Prolidase activity and oxidative status in patients with thalassemia major.

机构信息

Department of Pediatrics, Harran University School of Medicine, Sanliurfa, Turkey.

出版信息

J Clin Lab Anal. 2010;24(1):6-11. doi: 10.1002/jcla.20361.

DOI:10.1002/jcla.20361
PMID:20087956
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6647656/
Abstract

AIM

Prolidase is a specific imidodipeptidase involved in collagen degradation. The increase in the enzyme activity is believed to be correlated with the increased intensity of collagen degradation. The study aimed to evaluate the relationship between prolidase activity and oxidative status in patients with thalassemia major.

METHODS

Comparison was made between 87 patients diagnosed with thalassemia major and 33 healthy children of similar age and gender. Mean age of the subjects was 7.5+/-4.3 years in the group of patients with thalassemia major and 8.9+/-3.1 years in the control group. Serum prolidase activity was measured spectrophotometrically. Oxidative status was determined using total oxidant status (TOS), total antioxidant capacity (TAC), and oxidative stress index (OSI) measurement.

RESULTS

Prolidase activity was significantly increased in patients with thalassemia major (53.7+/-8.7 U/l) compared to the control group (49.2+/-7.2 U/l, P<0.001). TOS was significantly increased in the patient group (5.31+/-3.14 mmol H2O2 equiv./l) compared to the control group (3.49+/-2.98 mumol H2O2 equiv./l) and the OSI was also significantly increased in the patient group (3.86+/-3.28 arbitrary unit) compared to the control group (2.53+/-2.70 arbitrary unit) (P<0.0001 and P<0.001, respectively), while there were no significant differences between the patient (1.61+/-0.30 mumol Trolox equiv./l) and control (1.64+/-0.33 mumol Trolox equiv./l) groups with respect to TAC.

CONCLUSION

Significant increases in prolidase activity in patients with thalassemia major may constitute a key parameter in demonstrating a disorder of the collagen metabolism.

摘要

目的

脯肽酶是一种参与胶原降解的特异性二肽酶。该酶活性的增加被认为与胶原降解强度的增加有关。本研究旨在评估地中海贫血患者中脯肽酶活性与氧化状态之间的关系。

方法

比较了 87 例确诊的地中海贫血患者和 33 名年龄和性别相匹配的健康儿童。地中海贫血组患者的平均年龄为 7.5+/-4.3 岁,对照组为 8.9+/-3.1 岁。采用分光光度法测定血清脯肽酶活性。通过总氧化剂状态(TOS)、总抗氧化能力(TAC)和氧化应激指数(OSI)测定来确定氧化状态。

结果

与对照组(49.2+/-7.2 U/l,P<0.001)相比,地中海贫血患者的脯肽酶活性明显升高(53.7+/-8.7 U/l)。与对照组(3.49+/-2.98 mumol H2O2 equiv./l)相比,患者组的 TOS 明显升高(5.31+/-3.14 mmol H2O2 equiv./l),OSI 也明显升高(3.86+/-3.28 任意单位)与对照组(2.53+/-2.70 任意单位)相比(P<0.0001 和 P<0.001),而患者组(1.61+/-0.30 mumol Trolox equiv./l)与对照组(1.64+/-0.33 mumol Trolox equiv./l)之间的 TAC 无显著差异。

结论

地中海贫血患者脯肽酶活性的显著增加可能构成胶原代谢紊乱的一个关键参数。