Replication of 13q31.1 association in nonsyndromic cleft lip with cleft palate in Europeans. (18th March 2015)

• Record Type: Journal Article
• Authors: Jia, Zhonglin; Leslie, Elizabeth J.; Cooper, Margaret E.; Butali, Azeez; Standley, Jennifer; Rigdon, Jennifer; Suzuki, Satoshi; Gongorjav, Ayana; Shonkhuuz, T. Enkhtur; Natsume, Nagato; Shi, Bing; Marazita, Mary L.; Murray, Jeffrey C.
• Is Part Of: American journal of medical genetics. Volume 167:Number 5(2015:May)
• Page Start: 1054
• Page End: 1060
• Publication Date: 2015-03-18
• Subjects: Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.36912
• Languages: English
• ISSNs: 1552-4825

Abstract

<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="ajmga36912-sec-0001" sec-type="section"> <p>Genome wide association (GWA) studies have successfully identified at least a dozen loci associated with orofacial clefts. However, these signals may be unique to specific populations and require replication to validate and extend findings as a prelude to etiologic SNP discovery. We attempted to replicate the findings of a recent meta‐analysis of orofacial cleft GWA studies using four different ancestral populations. We studied 946 pedigrees (3, 436 persons) of European (US white and Danish) and Asian (Japanese and Mongolian) origin. We genotyped six SNPs that represented the most significant <italic>P</italic>‐value associations identified in published studies: rs742071 (1p36), rs7590268 (2p21), rs7632427 (3p11.1), rs12543318 (8q21.3), rs8001641 (13q31.1), and rs7179658 (15q22.2). We directly sequenced three non‐coding conserved regions 200 kb downstream of <italic>SPRY2</italic> in 713 cases, 438 controls, and 485 trios from the US, Mongolia, and the Philippines. We found rs8001641 to be significantly associated with nonsyndromic cleft lip with cleft palate (NSCLP) in Europeans (<italic>P</italic>‐value = 4 × 10<sup>−5</sup>, OR<sub>transmission</sub> = 1.86 with 95% confidence interval: 1.38–2.52). We also found several novel sequence variants in the conserved regions in Asian and European samples, which may help to localize common variants contributing directly to the risk for NSCLP. This study confirms the prior association between rs8001641 and NSCLP in European populations. © 2015 Wiley Periodicals, Inc.</p> </sec> </abstract>