Yamada Kyoko, Doi Shigehiro, Nakashima Ayumu, Kawaoka Koichiro, Ueno Toshinori, Doi Toshiki, Yokoyama Yukio, Arihiro Koji, Kohno Nobuoki, Masaki Takao
Department of Nephrology, Hiroshima University Hospital, 1-2-3 Kasumi, Minami-ku, Hiroshima, 734-8551, Japan.
Department of Regeneration and Medicine, Hiroshima University Hospital, Hiroshima, Japan.
Clin Exp Nephrol. 2015 Oct;19(5):830-7. doi: 10.1007/s10157-014-1070-2. Epub 2014 Dec 11.
Chronic kidney disease patients share clinical and pathological features with the general aging population. Increased oxidative DNA damage, accumulation of cell cycle-arrested cells and decreased Klotho expression are assumed to be age-related factors that are reportedly linked to kidney disease. This study sought to determine the association between these age-related factors and renal damage in patients with IgA nephropathy (IgAN).
We performed a cross-sectional analysis of 71 patients who were diagnosed with IgAN by renal biopsy. Expression of 8-hydroxydeoxyguanosine (8-OHdG, a marker of oxidative DNA damage), p16 (a marker of cell cycle-arrest) and Klotho (an anti-aging protein) were evaluated by immunohistochemical staining of renal biopsy samples. We correlated the changes in expression of these markers with Lee's pathologic grades and the Oxford classification. We also investigated the independent association between these markers and interstitial fibrosis using multiple linear regression analysis.
8-OHdG and p16 increased but Klotho decreased with progression of pathologic grade. Expression of 8-OHdG and p16 increased with the deterioration of mesangial hypercellularity and segmental glomerulosclerosis. In addition, p16 increased but Klotho decreased with progression of tubular atrophy/interstitial fibrosis. In univariate regression analysis, age, body mass index, systolic blood pressure, urinary protein excretion and expression of 8-OHdG, p16 and Klotho showed significant correlations with interstitial fibrosis. Multivariable regression analyses revealed that aging, increased renal expression of p16 and decreased expression of Klotho were independently correlated with interstitial fibrosis.
The age-related factors might play important roles in the development of IgAN.
慢性肾脏病患者与一般老年人群具有共同的临床和病理特征。氧化DNA损伤增加、细胞周期停滞细胞的积累以及Klotho表达降低被认为是与年龄相关的因素,据报道这些因素与肾脏疾病有关。本研究旨在确定这些与年龄相关的因素与IgA肾病(IgAN)患者肾损伤之间的关联。
我们对71例经肾活检诊断为IgAN的患者进行了横断面分析。通过对肾活检样本进行免疫组织化学染色,评估8-羟基脱氧鸟苷(8-OHdG,氧化DNA损伤的标志物)、p16(细胞周期停滞的标志物)和Klotho(一种抗衰老蛋白)的表达。我们将这些标志物表达的变化与Lee病理分级和牛津分类进行了关联分析。我们还使用多元线性回归分析研究了这些标志物与间质纤维化之间的独立关联。
随着病理分级的进展,8-OHdG和p16升高而Klotho降低。8-OHdG和p16的表达随着系膜细胞增多和节段性肾小球硬化的恶化而增加。此外,随着肾小管萎缩/间质纤维化的进展,p16升高而Klotho降低。在单变量回归分析中,年龄、体重指数、收缩压、尿蛋白排泄以及8-OHdG、p16和Klotho的表达与间质纤维化显著相关。多变量回归分析显示,衰老、肾脏p16表达增加和Klotho表达降低与间质纤维化独立相关。
与年龄相关的因素可能在IgAN的发生发展中起重要作用。