Treloar Susan, Hadfield Ruth, Montgomery Grant, Lambert Ann, Wicks Jacki, Barlow David H, O'Connor Daniel T, Kennedy Stephen
Cooperative Research Centre for Discovery of Genes for Common Human Diseases, Queensland Institute of Medical Research, Brisbane, Australia.
Fertil Steril. 2002 Oct;78(4):679-85. doi: 10.1016/s0015-0282(02)03341-1.
The aim of the International Endogene Study is to discover genes that influence susceptibility to endometriosis.
The study brings together two research groups based in Australia and the United Kingdom that independently have been collecting families for linkage analysis and candidate gene studies. Both groups used similar methods to recruit families, obtain clinical notes, assign disease status based on the operative records and available histology, and collect common clinical data including age at onset of symptoms, age at diagnosis, and symptoms experienced.
Recruitment has been mainly from Australia, the United Kingdom, and the United States.
PATIENT(S): All affected participants have surgically confirmed disease.
INTERVENTION(S): None.
MAIN OUTCOME MEASURE(S): Clinical and epidemiological data.
RESULT(S): To date, >1,100 families with affected sisters have been recruited, and >1,200 triads (affected women and both parents), for case-control studies.
CONCLUSION(S): We have created the largest resource yet assembled of clinical data and DNA for linkage and association studies in endometriosis. The increase in power to detect susceptibility genes vindicates the decision to merge the two studies and demonstrates the value of large-scale international collaboration.
国际内源性研究的目的是发现影响子宫内膜异位症易感性的基因。
该研究汇集了澳大利亚和英国的两个研究小组,这两个小组一直在独立收集家族进行连锁分析和候选基因研究。两个小组都使用类似的方法招募家族、获取临床记录、根据手术记录和可用的组织学结果确定疾病状态,并收集包括症状出现年龄、诊断年龄和经历的症状在内的常见临床数据。
招募主要来自澳大利亚、英国和美国。
所有受影响的参与者均经手术确诊患有该疾病。
无。
临床和流行病学数据。
迄今为止,已招募了超过1100个有患病姐妹的家族,以及超过1200个三联体(患病女性及其父母双方)用于病例对照研究。
我们已经创建了迄今为止最大的临床数据和DNA资源库,用于子宫内膜异位症的连锁和关联研究。检测易感基因能力的提高证明了合并两项研究的决定是正确的,并展示了大规模国际合作的价值。