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成人 ENPP1 缺乏症的临床表现和负担。

Clinical presentation and burden of ENPP1 deficiency in adults.

机构信息

Musculoskeletal Center Würzburg, University Hospital Würzburg, Brettreichstr. 11, 97074 Würzburg, Germany.

出版信息

Arch Pediatr. 2024 Sep;31(4S1):4S33-4S36. doi: 10.1016/S0929-693X(24)00155-6.

Abstract

While the clinical consequences of severe ENPP1 deficiency leading to the rare disorders generalized arterial calcification of infancy (GACI) and autosomal recessive hypophosphatemic rickets type 2 (ARHR2) are well defined and understood, much less is known about how this evolves into adulthood and how moderate ENPP1 deficiency can first manifest in adulthood. Moreover, growing evidence substantiates an association of genetic variants in the ENPP1 gene with a wide range of further clinical manifestations including early-onset osteoporosis, osteoarthritis, and different forms of spinal ligament calcifications, i.e., diffuse idiopathic skeletal hyperostosis (DISH) and ossification of the posterior/anterior longitudinal ligament (OPLL/OALL). Furthermore, conditions with primarily extraskeletal signs and symptoms such as Cole disease, coagulopathies, and metabolic syndrome can seemingly result from ENPP1 variants. The causality and the pathophysiology behind these different clinical presentations appear complex and require further research, especially since the coincidence of these different phenotypes is rarely described and available evidence suggests that part of the aforementioned manifestations may result from ENPP1 effects beyond the catalytic activity of processing ATP to AMP and inorganic pyrophosphate (PPi). Growing awareness of the additional ENPP1-related manifestations across the lifespan will advance our understanding of this complex condition and help to standardize diagnostic approaches and develop individually tailored treatment concepts.

摘要

尽管严重的 ENPP1 缺乏导致罕见疾病全身性动脉钙化症(GACI)和常染色体隐性低磷性佝偻病 2 型(ARHR2)的临床后果已经得到明确和理解,但对于这种疾病如何发展到成年期以及中度 ENPP1 缺乏症如何首先在成年期表现出来,人们知之甚少。此外,越来越多的证据证实,ENPP1 基因中的遗传变异与广泛的进一步临床表现有关,包括早发性骨质疏松症、骨关节炎和不同形式的脊柱韧带钙化,即弥漫性特发性骨肥厚(DISH)和后/前纵韧带骨化(OPLL/OALL)。此外,主要有骨骼外表现和症状的疾病,如科尔病、凝血障碍和代谢综合征,似乎也可以由 ENPP1 变异引起。这些不同临床表现背后的因果关系和病理生理学似乎很复杂,需要进一步研究,特别是因为这些不同表型的同时发生很少被描述,并且现有证据表明,上述部分表现可能是由于 ENPP1 除了将 ATP 转化为 AMP 和无机焦磷酸(PPi)的催化活性之外的作用所致。对整个生命周期中额外的与 ENPP1 相关表现的认识不断提高,将有助于我们理解这种复杂的疾病,并有助于标准化诊断方法和制定个体化的治疗方案。

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