Heritability of levels of autoantibodies to thyroid antigens using the method of plotting regression of offspring on midparent (ROMP)

被引:1
|
作者
Outschoorn, Ingrid M. [1 ]
Hoffman, William H.
Rose, Noel R.
Burek, C. Lynne
机构
[1] Inst Salud Carlos 3, Ctr Nacl Microbiol, Unidad Respuesta Inmune, Madrid 28220, Spain
[2] Med Coll Georgia, Dept Pediat, Sect Endocrinol, Augusta, GA 30912 USA
[3] Johns Hopkins Med Inst, Johns Hopkins Ctr Autoimmune Dis Res, Dept Pathol, Baltimore, MD 21205 USA
[4] Johns Hopkins Med Inst, Johns Hopkins Ctr Autoimmune Dis Res, Dept Mol Microbiol, Baltimore, MD 21205 USA
[5] Johns Hopkins Med Inst, Johns Hopkins Ctr Autoimmune Dis Res, Dept Immunol, Baltimore, MD 21205 USA
关键词
heritability; autoantibodies; thyroglobulin; thyroperoxidase; autoimmune thyroiditis; Graves' disease;
D O I
10.1080/08916930701394219
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Only a few methods can be applied in a simple manner to estimate the genetic control of autoimmunity in humans. Here we examined the heritability of autoantibodies to two thyroid antigens; thyroglobulin ( Tg) and thyroperoxidase (TPO, formerly known as thyroid microsomal antigen), using methods of regression of offspring on mid-parental values ( ROMP). With the data sets available, affected and unaffected siblings were compared by this rapid screening method using results determined by hemagglutination ( HA). The presence of both types of autoantibodies showed positive heritability in patients with Graves' thyrotoxicosis ( TT), but it was not observed in chronic lymphocytic or Hashimoto's thyroiditis (CLT) patients. Since these assays have been extensively used over the years by most diagnostic and research laboratories, they should provide some insight as to which quantifiable parameters may be usefully accumulated to help select groups of patients and their families for further genetic study. ROMP may also be useful to determine the sequential appearance of different types of antibody in predicting disease onset in other family members, and in distinguishing maternal and paternal effects on imprinting. The method may be extended to study epitope spreading and other measures of disease progression.
引用
收藏
页码:366 / 371
页数:6
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