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

被引:36
作者
Totonchy, Mariam B. [1 ,2 ]
Tamura, Deborah [1 ]
Pantell, Matthew S. [2 ,3 ]
Zalewski, Christopher [4 ]
Bradford, Porcia T. [5 ]
Merchant, Saumil N. [6 ]
Nadol, Joseph [6 ]
Khan, Sikandar G. [1 ]
Schiffmann, Raphael [7 ]
Pierson, Tyler Mark [7 ]
Wiggs, Edythe [7 ]
Griffith, Andrew J. [4 ]
DiGiovanna, John J. [1 ]
Kraemer, Kenneth H. [1 ]
Brewer, Carmen C. [4 ]
机构
[1] NCI, Dermatol Branch, Bethesda, MD 20892 USA
[2] NIH, Clin Res Training Programme, Bethesda, MD 20892 USA
[3] NIA, Lab Epidemiol Demog & Biometry, Bethesda, MD 20892 USA
[4] Natl Inst Deafness & Other Commun Disorders, Otolaryngol Branch, Bethesda, MD 20892 USA
[5] NCI, Genet Epidemiol Branch, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[6] Harvard Univ, Dept Otol & Laryngol, Massachusetts Eye & Ear Infirm, Sch Med, Boston, MA 02114 USA
[7] NINDS, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
xeroderma pigmentosum; sensorineural hearing loss; neurodegeneration; photosensitivity; DNA repair; COCKAYNE-SYNDROME; TRICHOTHIODYSTROPHY; DISEASE; MANIFESTATIONS; ABNORMALITIES; PHENOTYPE; SYMPTOMS; MUTATION; DEAFNESS; DAMAGE;
D O I
10.1093/brain/aws317
中图分类号
R74 [神经病学与精神病学];
学科分类号
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 epsilon 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.
引用
收藏
页码:194 / 208
页数:15
相关论文
共 45 条
  • [1] American National Standards Institute, 2003, ANSI S3.1-1999
  • [2] American National Standards Institute, 2004, S361996 ANSI
  • [3] Neurological symptoms and natural course of xeroderma pigmentosum
    Anttinen, Anu
    Koulu, Leena
    Nikoskelainen, Eeva
    Portin, Raija
    Kurki, Timo
    Erkinjuntti, Matti
    Jaspers, Nicolaas G. J.
    Raams, Anja
    Green, Michael H. L.
    Lehmann, Alan R.
    Wing, Jonathan F.
    Arlett, Colin F.
    Marttila, Reijo J.
    [J]. BRAIN, 2008, 131 : 1979 - 1989
  • [4] Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair
    Bradford, Porcia T.
    Goldstein, Alisa M.
    Tamura, Deborah
    Khan, Sikandar G.
    Ueda, Takahiro
    Boyle, Jennifer
    Oh, Kyu-Seon
    Imoto, Kyoko
    Inui, Hiroki
    Moriwaki, Shin-Ichi
    Emmert, Steffen
    Pike, Kristen M.
    Raziuddin, Arati
    Plona, Teri M.
    DiGiovanna, John J.
    Tucker, Margaret A.
    Kraemer, Kenneth H.
    [J]. JOURNAL OF MEDICAL GENETICS, 2011, 48 (03) : 168 - 176
  • [5] Ocular Manifestations of Trichothiodystrophy
    Brooks, Brian P.
    Thompson, Amy H.
    Clayton, Janine A.
    Chan, Chi-Chao
    Tamura, Deborah
    Zein, Wadih M.
    Blain, Delphine
    Hadsall, Casey
    Rowan, John
    Bowles, Kristen E.
    Khan, Sikandar G.
    Ueda, Takahiro
    Boyle, Jennifer
    Oh, Kyu-Seon
    DiGiovanna, John J.
    Kraemer, Kenneth H.
    [J]. OPHTHALMOLOGY, 2011, 118 (12) : 2335 - 2342
  • [6] Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage?
    Brooks, P. J.
    Cheng, Tsu-Fan
    Cooper, Lori
    [J]. DNA REPAIR, 2008, 7 (06) : 834 - 848
  • [7] Darrat Ilaaf, 2007, Curr Opin Otolaryngol Head Neck Surg, V15, P358, DOI 10.1097/MOO.0b013e3282efa641
  • [8] Neuropathological findings in eight children with cerebro-oculo-facio-skeletal (COFS) syndrome
    DelBigio, MR
    Greenberg, CR
    Rorke, LB
    Schnur, R
    McDonaldMcGinn, DM
    Zackai, EH
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1997, 56 (10) : 1147 - 1157
  • [9] Shining a Light on Xeroderma Pigmentosum
    DiGiovanna, John J.
    Kraemer, Kenneth H.
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2012, 132 (03) : 785 - 796
  • [10] Cerebro-oculo-facio-skeletal syndrome as a human example for accelerated cochlear nerve degeneration
    Fish, JH
    Scholtz, AW
    Hussl, B
    Kreczy, A
    Schrott-Fischer, A
    [J]. OTOLOGY & NEUROTOLOGY, 2001, 22 (02) : 170 - 177