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弹性假黄瘤患者的血浆无机焦磷酸和碱性磷酸酶

Plasma inorganic pyrophosphate and alkaline phosphatase in patients with pseudoxanthoma elasticum.

作者信息

Sánchez-Tévar Ana María, García-Fernández María, Murcia-Casas Belén, Rioja-Villodres José, Carrillo Juan Luis, Camacho Marta, Van Gils Matthias, Sánchez-Chaparro Miguel Angel, Vanakker Olivier, Valdivielso Pedro

机构信息

Lipid and Arteriosclerosis Laboratory, Centro de Investigaciones Médico-Sanitarias (CIMES), University of Málaga, Málaga, Spain.

Department of Physiology, Instituto de Investigación Biomédica de Málaga (IBIMA), University of Málaga, Málaga, Spain.

出版信息

Ann Transl Med. 2019 Dec;7(24):798. doi: 10.21037/atm.2019.12.73.

Abstract

BACKGROUND

Inorganic pyrophosphate (PPi) plays a major role inhibiting dystrophic calcification. The aim was to analyze levels of PPi in patients having pseudoxanthoma elasticum (PXE), and controls as well as the enzymes who regulate the PPi plasma concentration.

METHODS

We collected fasting blood samples from PXE patients and age- and sex-matched controls in ethylenediamine tetraacetic acid (EDTA) and citrate-theophylline-adenosine-dipyridamole (CTAD) containing tubes. We measured PPi, ENPP1 mass and activity, alkaline phosphatase (AP) and tissue non-specific alkaline phosphatase (TNAP), CD73 and Human Platelet Factor-4 (CXCL4).

RESULTS

PPi in EDTA and CTAD samples were lower in PXE subjects than in controls (1.11±0.26 1.43±0.41 µM/L and 0.35±0.15 0.61±0.18 µM/L respectively, P<0.05). TNAP and liver TNAP activities were also higher in PXE than in controls (80.3±27.0 63.3±16.4 UI/L and 25.6±14.9 12.9±9.2 UI/L respectively, P<0.05). ENPP1 mass and activity as well as CD73 were almost identical. There was a weak but significant inverse correlation between TNAP activity and PPi levels (Pearson correlation -0.379, P<0.05) in both groups.

CONCLUSIONS

High TNAP activity seems to contribute to low plasma levels of PPi in subjects with PXE, reinforcing the idea that pharmacological reduction of TNAP activity may help to reduce dystrophic calcification in PXE patients.

摘要

背景

无机焦磷酸(PPi)在抑制营养不良性钙化中起主要作用。目的是分析弹性假黄瘤(PXE)患者、对照组以及调节PPi血浆浓度的酶的PPi水平。

方法

我们从PXE患者以及年龄和性别匹配的对照组中采集空腹血样,血样采集于含有乙二胺四乙酸(EDTA)和枸橼酸盐 - 茶碱 - 腺苷 - 双嘧达莫(CTAD)的试管中。我们测量了PPi、ENPP1的质量和活性、碱性磷酸酶(AP)和组织非特异性碱性磷酸酶(TNAP)、CD73和人血小板因子4(CXCL4)。

结果

PXE受试者的EDTA和CTAD样本中的PPi低于对照组(分别为1.11±0.26对1.43±0.41μM/L和0.35±0.15对0.61±0.18μM/L,P<0.05)。PXE患者的TNAP和肝脏TNAP活性也高于对照组(分别为80.3±27.0对63.3±16.4 UI/L和25.6±14.9对12.9±9.2 UI/L,P<0.05)。ENPP1的质量和活性以及CD73几乎相同。两组中TNAP活性与PPi水平之间均存在微弱但显著的负相关(Pearson相关性为 -0.379,P<0.05)。

结论

高TNAP活性似乎导致PXE患者血浆PPi水平降低,这强化了药理学降低TNAP活性可能有助于减少PXE患者营养不良性钙化的观点。

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本文引用的文献

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5
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J Invest Dermatol. 2018 Aug;138(8):1862-1870. doi: 10.1016/j.jid.2018.02.023. Epub 2018 Mar 6.
7
Oral administration of pyrophosphate inhibits connective tissue calcification.
EMBO Mol Med. 2017 Nov;9(11):1463-1470. doi: 10.15252/emmm.201707532.
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J Invest Dermatol. 2017 Nov;137(11):2336-2343. doi: 10.1016/j.jid.2017.06.006. Epub 2017 Jun 23.
10
Inherited Arterial Calcification Syndromes: Etiologies and Treatment Concepts.
Curr Osteoporos Rep. 2017 Aug;15(4):255-270. doi: 10.1007/s11914-017-0370-3.

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