Hypodontia as a risk marker for epithelial ovarian cancer - A case-controlled study

被引:40
作者
Chalothorn, Leigh A.
Beeman, Cynthia S. [1 ]
Ebersole, Jeffrey L. [2 ]
Kluemper, G. Thomas [1 ]
Hicks, Preston [1 ]
Kryscio, Richard J. [3 ]
DeSimone, Christopher P. [2 ]
Modesitt, Susan C. [4 ]
机构
[1] Univ Kentucky, Div Orthodont, Lexington, KY USA
[2] Univ Kentucky, Ctr Oral & Hlth Res, Lexington, KY USA
[3] Univ Kentucky, Dept Biostat, Coll Publ Hlth, Lexington, KY USA
[4] Univ Virginia, Charlottesville, VA USA
关键词
ovarian cancer; DNA; hypodontia; genetics; tooth;
D O I
10.14219/jada.archive.2008.0132
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background. Genetic mutations that result in F hypodontia also may be associated with abnormalities in other parts of the body. The authors conducted a study to establish the prevalence rates of hypodontia among subjects with epithelial ovarian cancer (EOC) and control subjects to explore possible genetic associations between these two phenotypes. Methods. The authors recruited 50 subjects with EOC and 100 control subjects who did not have EOC. The authors performed a dental examination on each subject to detect hypodontia, and they reviewed pertinent radiographs and dental histories. They also recorded any family history of cancer and hypodontia. Results: The prevalence of hypodontia was 20 percent for EOC subjects and 3 percent for control subjects. The difference between these two hypodontia rates was significant. This difference implied that women with EOC are 8.1 times more likely to have hypodontia than are women without EOC. The severity of hypodontia was similar between the two groups, with one to two teeth being affected. Maxillary lateral incisors followed by second premolars were the most frequently affected teeth. Conclusion. The preliminary data suggest a statistical association between hypodontia of the permanent dentition and EOC. Clinical Implications. Genetic analysis of the genes of interest is necessary to explore similarities between hypodontia and EOC further: An association could allow hypodontia to serve as a potential risk marker for EOC.
引用
收藏
页码:163 / 169
页数:7
相关论文
共 36 条
  • [1] Msx homeobox gene family and craniofacial development
    Alappat, S
    Zhang, ZY
    Chen, YP
    [J]. CELL RESEARCH, 2003, 13 (06) : 429 - 442
  • [2] Bast Robert C. Jr., 2007, V174, P91
  • [3] A UNIFYING ETIOLOGICAL EXPLANATION FOR ANOMALIES OF HUMAN TOOTH NUMBER AND SIZE
    BROOK, AH
    [J]. ARCHIVES OF ORAL BIOLOGY, 1984, 29 (05) : 373 - 378
  • [4] Chen YP, 1996, DEVELOPMENT, V122, P3035
  • [5] A novel mutation in human PAX9 causes molar oligodontia
    Frazier-Bowers, SA
    Guo, DC
    Cavender, A
    Xue, L
    Evans, B
    King, T
    Milewicz, D
    D'Souza, RN
    [J]. JOURNAL OF DENTAL RESEARCH, 2002, 81 (02) : 129 - 133
  • [6] Progressive loss of PAX9 expression correlates with increasing malignancy of dysplastic and cancerous epithelium of the human oesophagus
    Gerber, JK
    Richter, T
    Kremmer, E
    Adamski, J
    Höfler, H
    Balling, R
    Peters, H
    [J]. JOURNAL OF PATHOLOGY, 2002, 197 (03) : 293 - 297
  • [7] Barx2, a new homeobox gene of the Bar class, is expressed in neural and craniofacial structures during development
    Jones, FS
    Kioussi, C
    Copertino, DW
    Kallunki, P
    Holst, BD
    Edelman, GM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) : 2632 - 2637
  • [8] A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia
    Jumlongras, D
    Lin, JY
    Chapra, A
    Seidman, CE
    Seidman, JG
    Maas, RL
    Olsen, BR
    [J]. HUMAN GENETICS, 2004, 114 (03) : 242 - 249
  • [9] Novel mutation of the initiation codon of PAX9 causes oligodontia
    Klein, ML
    Nieminen, P
    Lammi, L
    Niebuhr, E
    Kreiborg, S
    [J]. JOURNAL OF DENTAL RESEARCH, 2005, 84 (01) : 43 - 47
  • [10] KOLENC-FUSE F., 2004, MED ORAL PATOL ORAL, V2, P385