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

机译:1971年至2012年色素干皮症的听觉分析:听力功能太阳敏感性和DNA修复可预测神经系统退化

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摘要

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.
机译:为了评估DNA修复在维持听觉功能和神经系统完整性中的作用,我们检查了所有色素性干皮病患者的听力状况,神经功能,DNA修复补体组和在极少阳光照射下急性灼伤的病史,这些患者至少有一名听力图,于1971年至2012年在美国国立卫生研究院进行了检查。有79名1至61岁的患者被诊断患有色素性干皮病(n = 77)或色素性干皮病/ Cockayne综合征(n = 2)。总共包括178个听力图。 79例患者中有23例(29%)存在临床上明显的听力损失(> 20 dB)。在17例皮肤干燥性色素变性的神经系统疾病患者中,有13例(76%)发生了听力丧失,所有17例均属于A组或D型皮肤干燥性色素的补充组,并且在极少暴露于阳光下时出现急性灼伤。 18%的患者中出现了急性灼伤,暴露在最低限度的阳光下,而没有干性色素性皮肤病。患有严重干性色素干性皮肤型神经变性的患者的颞骨组织学表现为耳蜗感觉上皮和神经元明显萎缩。患有皮肤干燥色素性神经变性的干燥皮肤色素变性患者的19岁平均临床检测听力下降年龄比国际规范所预测的年龄低54岁。四个频率(0.5 / 1/2/4 kHz)的纯音平均值与神经变性程度相关(P <0.001)。在4至30岁的干性皮肤色素性皮肤病患者中,四频纯音平均≥10 dB听力损失会导致干性皮肤色素性皮肤病神经变性的风险增加39倍(P = 0.002)。严重的听力损失与干性色素性皮肤干燥性神经变性患者的神经功能下降平行。听力测验结果,补体组,在最低限度的阳光照射下急性灼伤和年龄是干性色素性皮肤型神经系统变性的重要预测指标。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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