Department of Gastroenterology, Erciyes University, Kayseri, Turkey.
Digestion. 2012;85(3):228-35. doi: 10.1159/000336358. Epub 2012 Mar 29.
The present study aimed to evaluate the micronucleus (MN), nucleoplasmic bridges (NPBs) and nuclear buds (NBUDs) in the mitogen-stimulated lymphocytes of patients with ulcerative colitis (UC). In addition, we assessed MN frequency in exfoliated colonic epithelial cells obtained from both the diseased and healthy colonic mucosa of patients.
The study was conducted in 22 newly diagnosed patients with UC and in 22 healthy controls. MN, NPB and NBUD values scored in binucleated (BN) cells were obtained from the mitogen-stimulated lymphocytes of patients and control subjects. In addition, the MN values in exfoliated epithelial cells obtained from the diseased and healthy colonic mucosa of patients were evaluated.
We found significantly higher MN, NPB and NBUD frequencies in the BN cells of patients with UC than in those of the control subjects (1.61 ± 0.75 vs. 0.89 ± 0.29, 3.93 ± 1.91 vs. 1.39 ± 1.10, and 1.55 ± 0.89 vs. 0.64 ± 0.48, p = 0.001). Also, a statistically significant difference was found between MN frequencies obtained from the diseased and healthy colonic mucosa of patients (1.07 ± 0.46 vs. 0.59 ± 0.21, p = 0.001). No significant relationship was found between age and MN frequency in patients with UC (r = 0.076, p = 0.735).
Increased MN, NPB and NBUD frequencies observed in both the lymphocytes and exfoliated colonic epithelial cells obtained from patients with UC may reflect genomic instability.
本研究旨在评估溃疡性结肠炎(UC)患者刺激淋巴细胞中的微核(MN)、核质桥(NPB)和核芽(NBUD),并评估从患者病变和正常结肠黏膜脱落的结肠上皮细胞中的 MN 频率。
本研究纳入 22 例新诊断的 UC 患者和 22 例健康对照者。从患者和对照者的刺激淋巴细胞中获取双核细胞(BN)的 MN、NPB 和 NBUD 值。此外,还评估了从患者病变和正常结肠黏膜脱落的上皮细胞中的 MN 值。
与对照组相比,UC 患者 BN 细胞中的 MN、NPB 和 NBUD 频率明显更高(1.61 ± 0.75 比 0.89 ± 0.29,3.93 ± 1.91 比 1.39 ± 1.10,1.55 ± 0.89 比 0.64 ± 0.48,p = 0.001)。此外,还发现患者病变和正常结肠黏膜的 MN 频率之间存在统计学差异(1.07 ± 0.46 比 0.59 ± 0.21,p = 0.001)。UC 患者的年龄与 MN 频率之间无显著相关性(r = 0.076,p = 0.735)。
UC 患者刺激淋巴细胞和脱落的结肠上皮细胞中 MN、NPB 和 NBUD 频率的增加可能反映了基因组不稳定性。