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2012 年对色素性干皮病 1971-1971 年的听觉分析:听力功能、对阳光的敏感和 DNA 修复预测神经退行性变。

Auditory analysis of xeroderma pigmentosum 1971-2012: hearing function, sun sensitivity and DNA repair predict neurological degeneration.

机构信息

Dermatology Branch, National Cancer Institute, Bethesda, MD 20892, USA.

出版信息

Brain. 2013 Jan;136(Pt 1):194-208. doi: 10.1093/brain/aws317.

Abstract

To assess the role of DNA repair in maintenance of hearing function and neurological integrity, we examined hearing status, neurological function, DNA repair complementation group and history of acute burning on minimal sun exposure in all patients with xeroderma pigmentosum, who had at least one complete audiogram, examined at the National Institutes of Health from 1971 to 2012. Seventy-nine patients, aged 1-61 years, were diagnosed with xeroderma pigmentosum (n = 77) or xeroderma pigmentosum/Cockayne syndrome (n = 2). A total of 178 audiograms were included. Clinically significant hearing loss (>20 dB) was present in 23 (29%) of 79 patients. Of the 17 patients with xeroderma pigmentosum-type neurological degeneration, 13 (76%) developed hearing loss, and all 17 were in complementation groups xeroderma pigmentosum type A or type D and reported acute burning on minimal sun exposure. Acute burning on minimal sun exposure without xeroderma pigmentosum-type neurological degeneration was present in 18% of the patients (10/55). Temporal bone histology in a patient with severe xeroderma pigmentosum-type neurological degeneration revealed marked atrophy of the cochlear sensory epithelium and neurons. The 19-year mean age of detection of clinically significant hearing loss in the patients with xeroderma pigmentosum with xeroderma pigmentosum-type neurological degeneration was 54 years younger than that predicted by international norms. The four frequency (0.5/1/2/4 kHz) pure-tone average correlated with degree of neurodegeneration (P < 0.001). In patients with xeroderma pigmentosum, aged 4-30 years, a four-frequency pure-tone average ≥10 dB hearing loss was associated with a 39-fold increased risk (P = 0.002) of having xeroderma pigmentosum-type neurological degeneration. Severity of hearing loss parallels neurological decline in patients with xeroderma pigmentosum-type neurological degeneration. Audiometric findings, complementation group, acute burning on minimal sun exposure and age were important predictors of xeroderma pigmentosum-type neurological degeneration. These results provide evidence that DNA repair is critical in maintaining neurological integrity of the auditory system.

摘要

为了评估 DNA 修复在维持听力功能和神经完整性方面的作用,我们检查了所有患有着色性干皮病的患者的听力状况、神经功能、DNA 修复互补组和最小阳光暴露下急性灼伤的病史,这些患者均在 1971 年至 2012 年期间在国立卫生研究院接受了至少一次完整的听力测试。共有 79 名年龄在 1-61 岁的患者被诊断为着色性干皮病(n = 77)或着色性干皮病/Cockayne 综合征(n = 2)。共纳入 178 次听力测试。79 名患者中有 23 名(29%)存在临床显著听力损失(>20dB)。在 17 名患有着色性干皮病型神经退行性变的患者中,13 名(76%)出现听力损失,且所有 17 名患者均属于着色性干皮病 A 型或 D 型互补组,并报告最小阳光暴露下急性灼伤。在没有着色性干皮病型神经退行性变的情况下,18%的患者(10/55)存在最小阳光暴露下急性灼伤。一名严重着色性干皮病型神经退行性变患者的颞骨组织学检查显示耳蜗感觉上皮和神经元明显萎缩。患有着色性干皮病型神经退行性变的患者中,临床显著听力损失的 19 年平均检出年龄比国际标准预测的早 54 岁。四个频率(0.5/1/2/4kHz)纯音平均与神经退行性变程度相关(P<0.001)。在 4-30 岁的着色性干皮病患者中,四个频率纯音平均≥10dB 听力损失与 39 倍的着色性干皮病型神经退行性变风险增加相关(P=0.002)。听力损失的严重程度与着色性干皮病型神经退行性变患者的神经衰退程度平行。听力测试结果、互补组、最小阳光暴露下的急性灼伤和年龄是着色性干皮病型神经退行性变的重要预测因素。这些结果提供了证据,表明 DNA 修复对于维持听觉系统的神经完整性至关重要。

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