Clinical and biochemical characterization of a patient with prolidase deficiency, a rare disorder of collagen metabolism

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Troy K. Coody , Irene De Biase , Julie M. Porter , Marzia Pasquali , Brian J. Shayota
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引用次数: 0

Abstract

Prolidase deficiency (PD) is an autosomal recessive inborn error of metabolism, with an estimated incidence of 1 per 1.25 million births. Prolidase is critical for the turnover of proline and hydroxyproline-rich proteins, such as collagen. Collagen metabolism is essential for matrix regeneration during cellular proliferation and complex bodily functions such as wound healing and immunological cell differentiation. PD clinical manifestations include persistent skin ulcerations and poor wound healing, hypertelorism, high arched palate, depressed nasal bridge, micrognathia, splenomegaly, intellectual disability, recurring infections, and hematological abnormalities. Biochemically, a diagnosis of PD is supported by increased urinary excretion of glycyl-proline and other proline-containing iminopeptides detected by amino acid analysis. There are no current targeted therapies, but suggested interventions have included topical proline-glycine ointment, manganese supplementation, topical and oral steroids, and immunomodulation with monoclonal antibodies.
Here, we describe a 30-year-old patient with PD whose clinical course has been characterized by recurrent skin ulcerations/cysts with secondary scarring, recurrent infections, anemia, thrombocytopenia, lymphopenia, elevated liver enzymes, hirsutism, and seemingly unrelated papillary thyroid cancer. Skin manifestations were particularly severe due to the added complication of a diagnosis of hidradenitis suppurativa. Quantitative analysis of amino acids and related compounds revealed markedly elevated glycyl-proline in urine and plasma. To further characterize the biochemical phenotype, untargeted metabolomic analysis was sent on both plasma and urine. An increase was noted in several metabolites from the prolidase-dependent dipeptide recycling pathways. A better understanding of the pathophysiological mechanisms involved in prolidase deficiency may prove useful as different therapeutic approaches are being considered.
1例罕见的胶原代谢紊乱——蛋白酶缺乏症的临床及生化特征分析
脯氨酸酶缺乏症(PD)是一种常染色体隐性遗传的先天性代谢错误,估计发病率为每125万新生儿中有1例。脯氨酸酶对脯氨酸和富含羟基脯氨酸的蛋白质(如胶原蛋白)的转化至关重要。在细胞增殖和复杂的身体功能,如伤口愈合和免疫细胞分化过程中,胶原代谢对基质再生至关重要。PD的临床表现包括持续性皮肤溃疡和伤口愈合不良、远端肥大、上颚高弓、鼻桥凹陷、小颌、脾肿大、智力残疾、反复感染和血液系统异常。从生化角度看,尿中甘氨酸-脯氨酸和其他含有脯氨酸的亚胺肽的排泄量增加,可以通过氨基酸分析来诊断PD。目前尚无靶向治疗,但建议的干预措施包括外用脯氨酸-甘氨酸软膏、锰补充剂、外用和口服类固醇以及单克隆抗体免疫调节。在这里,我们描述了一位30岁的PD患者,其临床过程的特征是复发性皮肤溃疡/囊肿伴继发性瘢痕形成,复发性感染,贫血,血小板减少,淋巴细胞减少,肝酶升高,多毛和看似无关的甲状腺乳头状癌。由于化脓性汗腺炎的附加并发症,皮肤表现特别严重。氨基酸和相关化合物的定量分析显示,尿和血浆中甘氨酸显著升高。为了进一步表征生化表型,对血浆和尿液进行了非靶向代谢组学分析。来自脯氨酸酶依赖性二肽循环途径的几种代谢物增加。更好地了解与脯氨酸酶缺乏症有关的病理生理机制可能会被证明是有用的,因为正在考虑不同的治疗方法。
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来源期刊
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports Biochemistry, Genetics and Molecular Biology-Endocrinology
CiteScore
4.00
自引率
5.30%
发文量
105
审稿时长
33 days
期刊介绍: Molecular Genetics and Metabolism Reports is an open access journal that publishes molecular and metabolic reports describing investigations that use the tools of biochemistry and molecular biology for studies of normal and diseased states. In addition to original research articles, sequence reports, brief communication reports and letters to the editor are considered.
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