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结节病患者肾功能障碍时 1,25 二羟维生素 D 增加。

Increase of 1,25 dihydroxyvitamin D in sarcoidosis patients with renal dysfunction.

机构信息

Nephrology Center, Toranomon Hospital, Tokyo, Japan.

Nephrology Center, Toranomon Hospital Kajigaya, 1-3-1, Takatsu, Kawasaki, 212-0015, Kanagawa, Japan.

出版信息

Clin Exp Nephrol. 2019 Oct;23(10):1202-1210. doi: 10.1007/s10157-019-01760-3. Epub 2019 Jun 25.

DOI:10.1007/s10157-019-01760-3
PMID:31240503
Abstract

INTRODUCTION

In sarcoidosis, renal involvement includes hypercalcemia-related nephrocalcinosis and granulomatous tubulointerstitial nephritis. Hypercalcemia is thought to be due to increased production of 1,25 dihydroxyvitamin D (1-25D), but 1-25D levels have not been evaluated in sarcoidosis patients with renal dysfunction.

MATERIALS AND METHODS

We enrolled 9 sarcoidosis patients who underwent renal biopsy, and compared the serum 1-25D concentration and eGFR with those in 428 non-sarcoidosis patients who had renal dysfunction (stage 2 or higher CKD with an estimated glomerular filtration rate < 90).

RESULTS

Serum calcium and 1-25D levels were significantly higher in the sarcoidosis patients than in the non-sarcoidosis patients (p < 0.01 and p = 0.01, respectively). There was a positive correlation between 1-25D and eGFR in the patients without sarcoidosis (r = 0.693; p < 0.01). As the renal function of sarcoidosis patients was improved by steroid therapy, the serum 1-25D and adjusted serum calcium levels decreased to near the median values in non-sarcoidosis patients. On renal biopsy, CD68 staining was positive for tissue macrophages in all 8 patients who had tubulointerstitial nephritis (with or without typical granulomas), while Von Kossa staining showed calcification of tubules near or inside granulomas in 6 of these 8 patients.

CONCLUSION

While tissue macrophages promote development of tubulointerstitial nephritis and 1-25D overproduction in renal sarcoidosis, hypercalcemia secondary to elevation of 1-25D may be related to renal calcification and granuloma formation.

摘要

介绍

在结节病中,肾脏受累包括高钙血症相关的肾钙质沉着症和肉芽肿性肾小管间质性肾炎。高钙血症被认为是由于 1,25 二羟维生素 D(1-25D)的产生增加所致,但在肾功能障碍的结节病患者中尚未评估 1-25D 水平。

材料和方法

我们纳入了 9 名接受肾活检的结节病患者,并将其血清 1-25D 浓度和 eGFR 与 428 名患有肾功能障碍(2 期或更高 CKD,估计肾小球滤过率<90)的非结节病患者进行了比较。

结果

与非结节病患者相比,结节病患者的血清钙和 1-25D 水平显著升高(p<0.01 和 p=0.01)。在无结节病患者中,1-25D 与 eGFR 呈正相关(r=0.693;p<0.01)。随着类固醇治疗改善结节病患者的肾功能,血清 1-25D 和校正血清钙水平降低至接近非结节病患者的中位数。在肾活检中,所有 8 例存在肾小管间质性肾炎(伴有或不伴有典型肉芽肿)的患者的组织巨噬细胞 CD68 染色均为阳性,而在这 8 例患者中的 6 例,Von Kossa 染色显示肉芽肿附近或内部的肾小管钙化。

结论

虽然组织巨噬细胞促进了结节病的肾小管间质性肾炎和 1-25D 的过度产生,但继发于 1-25D 升高的高钙血症可能与肾钙化和肉芽肿形成有关。

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