Temporomandibular Disorder-Type Pain and Migraine Headache in Women: A Preliminary Twin Study

被引:0
作者
Plesh, Octavia [1 ]
Noonan, Carolyn [2 ]
Buchwald, Dedra S. [2 ]
Goldberg, Jack [3 ]
Afari, Niloo [4 ,5 ]
机构
[1] Univ Calif San Francisco, Dept Prevent & Restorat Dent Sci, San Francisco, CA 94143 USA
[2] Univ Washington, Dept Med, Seattle, WA USA
[3] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[4] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92103 USA
[5] VA Ctr Excellence Stress & Mental Hlth, San Diego, CA USA
来源
JOURNAL OF OROFACIAL PAIN | 2012年 / 26卷 / 02期
基金
美国国家卫生研究院;
关键词
SEROTONIN TRANSPORTER GENE; FAMILIAL RISK; SELF-REPORT; POPULATION; ZYGOSITY; POLYMORPHISM; REGISTRY; SENSITIVITY; PREVALENCE; DEPRESSION;
D O I
暂无
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aims: To determine whether shared genetic influences are responsible for the association between pain from temporomandibular disorders (TMD) and migraine headache. Methods: Data were obtained from 1,236 monozygotic and 570 dizygotic female twin pairs from the University of Washington Twin Registry. TMD pain was assessed with a question about persistent or recurrent pain in the jaw, temple, in front of the ear, or in the ear. The presence of migraine headache was determined by self-report of doctor-diagnosed migraine. Univariate and bivariate structural equation models estimated the components of variance attributable to genetic and environmental influences. Results: The best fitting univariate models indicated that additive genetic effects contributed 27% of the variance in TMD pain (95% confidence interval = 15% to 38%) and 49% of the variance in migraine headache (95% confidence interval = 40% to 57%). The best-fitting bivariate model revealed that 12% of the genetic component of TMD pain is shared with migraine headache. Conclusion: These preliminary findings suggest that the association between TMD pain and migraine headache in women may be partially due to a modest shared genetic risk for both conditions. Future studies can focus on replicating these findings with symptom- and diagnosis-based instruments. J OROFAC PAIN 2012;26:91-98
引用
收藏
页码:91 / 98
页数:8
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