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Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.


ABSTRACT: Recurrent miscarriage (RM) affects millions of couples globally, and half of them have no demonstrated etiology. Genome sequencing (GS) is an enhanced and novel cytogenetic tool to define the contribution of chromosomal abnormalities in human diseases. In this study we evaluated its utility in RM-affected couples. We performed low-pass GS retrospectively for 1,090 RM-affected couples, all of whom had routine chromosome analysis. A customized sequencing and interpretation pipeline was developed to identify chromosomal rearrangements and deletions/duplications with confirmation by fluorescence in situ hybridization, chromosomal microarray analysis, and PCR studies. Low-pass GS yielded results in 1,077 of 1,090 couples (98.8%) and detected 127 chromosomal abnormalities in 11.7% (126/1,077) of couples; both members of one couple were identified with inversions. Of the 126 couples, 39.7% (50/126) had received former diagnostic results by karyotyping characteristic of normal human male or female karyotypes. Low-pass GS revealed additional chromosomal abnormalities in 50 (4.0%) couples, including eight with balanced translocations and 42 inversions. Follow-up studies of these couples showed a higher miscarriage/fetal-anomaly rate of 5/10 (50%) compared to 21/93 (22.6%) in couples with normal GS, resulting in a relative risk of 2.2 (95% confidence interval, 1.1 to 4.6). In these couples, this protocol significantly increased the diagnostic yield of chromosomal abnormalities per couple (11.7%) in comparison to chromosome analysis (8.0%, chi-square test p = 0.000751). In summary, low-pass GS identified underlying chromosomal aberrations in 1 in 9 RM-affected couples, enabling identification of a subgroup of couples with increased risk of subsequent miscarriage who would benefit from a personalized intervention.

SUBMITTER: Dong Z 

PROVIDER: S-EPMC6904795 | biostudies-literature | 2019 Dec

REPOSITORIES: biostudies-literature

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Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.

Dong Zirui Z   Yan Junhao J   Xu Fengping F   Yuan Jianying J   Jiang Hui H   Wang Huilin H   Chen Haixiao H   Zhang Lei L   Ye Lingfei L   Xu Jinjin J   Shi Yuhua Y   Yang Zhenjun Z   Cao Ye Y   Chen Lingyun L   Li Qiaoling Q   Zhao Xia X   Li Jiguang J   Chen Ao A   Zhang Wenwei W   Wong Hoi Gin HG   Qin Yingying Y   Zhao Han H   Chen Yuan Y   Li Pei P   Ma Tao T   Wang Wen-Jing WJ   Kwok Yvonne K YK   Jiang Yuan Y   Pursley Amber N AN   Chung Jacqueline P W JPW   Hong Yan Y   Kristiansen Karsten K   Yang Huanming H   Piña-Aguilar Raul E RE   Leung Tak Yeung TY   Cheung Sau Wai SW   Morton Cynthia C CC   Choy Kwong Wai KW   Chen Zi-Jiang ZJ  

American journal of human genetics 20191031 6


Recurrent miscarriage (RM) affects millions of couples globally, and half of them have no demonstrated etiology. Genome sequencing (GS) is an enhanced and novel cytogenetic tool to define the contribution of chromosomal abnormalities in human diseases. In this study we evaluated its utility in RM-affected couples. We performed low-pass GS retrospectively for 1,090 RM-affected couples, all of whom had routine chromosome analysis. A customized sequencing and interpretation pipeline was developed t  ...[more]

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