Department of Nephrology, The Royal Melbourne Hospital, 300 Grattan St, Parkville, Victoria, 3050, Australia.
Department of Medicine (RMH), The University of Melbourne, Parkville, Victoria, Australia.
BMC Nephrol. 2020 Jul 16;21(1):279. doi: 10.1186/s12882-020-01928-0.
Vascular calcification (VC) is well described in large- and medium-sized vessels in patients with chronic kidney disease (CKD), especially in those with end-stage kidney disease (ESKD) on dialysis. Medial calcification is particularly prevalent in this population and contributes to arterial stiffness and increased cardiovascular mortality and morbidity. Apart from in the setting of calciphylaxis, few studies have assessed skin and subcutaneous calcification and associations with abnormalities of bone and mineral metabolism in patients with CKD.
We performed a single-centre observational study to evaluate incisional skin tissue samples from three anatomical sites in patients with different stages of CKD undergoing elective surgery. We compared these samples to skin samples of a control cohort without CKD. Staining for calcification was performed with von Kossa method. A subgroup of skin samples were assessed by RT-PCR for upregulation of pro-calcific gene transcripts for tissue non-specific alkaline phosphatase (TNAP) and Runt-related transcription factor 2 (RUNX2).
Forty-five patients were evaluated, 34 with CKD (including ESKD) and 11 control patients. VC was identified in 15 skin samples (13 CKD/ESKD and 2 controls). VC was present in the dermal and subcutaneous tissues of the neck, abdomen and arm samples. Two different histological types of VC were identified: speckled medial calcification and internal elastic lamina calcification. Presence of perieccrine calcification was identified in 14 samples, 10 with concurrent VC. There were no significant differences in serum parathyroid hormone, phosphate or calcium in patients with or without VC. Expression of TNAP or RUNX2 was not increased in samples from patients with ESKD or those with histological evidence of calcification.
This study reports the novel finding of dermal and subcutaneous calcification in multiple anatomical locations in 38% of patients with advanced CKD/ESKD undergoing elective surgery but free from calciphylaxis.
血管钙化(VC)在慢性肾脏病(CKD)患者的大、中血管中已有详细描述,尤其是在接受透析的终末期肾病(ESKD)患者中。这种人群中普遍存在中层钙化,导致动脉僵硬和心血管死亡率和发病率增加。除了钙化磷灰石症外,很少有研究评估 CKD 患者的皮肤和皮下钙化以及与骨和矿物质代谢异常的关系。
我们进行了一项单中心观察性研究,以评估接受择期手术的不同 CKD 阶段患者三个解剖部位的切口皮肤组织样本。我们将这些样本与无 CKD 的对照组皮肤样本进行比较。采用 von Kossa 法对钙化进行染色。皮肤样本的亚组通过 RT-PCR 评估组织非特异性碱性磷酸酶(TNAP)和 runt 相关转录因子 2(RUNX2)的促钙化基因转录本的上调。
共评估了 45 例患者,34 例为 CKD(包括 ESKD),11 例为对照组患者。15 例皮肤样本中发现 VC(13 例 CKD/ESKD 和 2 例对照组)。VC 存在于颈部、腹部和手臂样本的真皮和皮下组织中。确定了两种不同类型的 VC:点状中层钙化和内弹性膜钙化。在 14 例样本中发现了周围细胞钙化,其中 10 例同时存在 VC。VC 患者与无 VC 患者的血清甲状旁腺激素、磷酸盐或钙无显著差异。ESKD 患者或有组织学钙化证据的患者样本中 TNAP 或 RUNX2 的表达没有增加。
本研究报告了一项新发现,即在接受择期手术的 38%的晚期 CKD/ESKD 患者的多个解剖部位存在皮肤和皮下钙化,但无钙化磷灰石症。