Mani Arya, Meraji Seyed-Mahmoud, Houshyar Roozbeh, Radhakrishnan Jayaram, Mani Alaleh, Ahangar Mehrabeh, Rezaie Tayebeh M, Taghavinejad Mohammad-Ali, Broumand Behrooz, Zhao Hongyu, Nelson-Williams Carol, Lifton Richard P
Department of Medicine and Genetics, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT 06510, USA.
Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):15054-9. doi: 10.1073/pnas.192582999. Epub 2002 Oct 30.
The causes of many sporadic diseases are unexplained; the contribution of recessive loci with reduced penetrance is one possibility that has been difficult to explore. We describe an approach to this problem by first searching for diseases with higher prevalence in populations with high rates of consanguinity, then determining whether disease cases are more commonly the product of consanguinous union than controls in such populations, followed by analysis of genetic linkage in consanguinous cases. We demonstrate the utility of this approach by investigation of congenital heart disease in Iran. We found that patent ductus arteriosus (PDA), a common congenital heart disease, accounts for a higher fraction of congenital heart disease in Iran (15%) than in the United States (2-7%). Moreover, Iranian PDA cases demonstrated a marked increase of parental consanguinity (63%), compared with the general Iranian population (25%) or control cases with tetralogy of Fallot (30%). The recurrence of PDA among siblings was 5%. A genomewide analysis of linkage in 21 unrelated consanguinous PDA cases demonstrated a multipoint logarithm of odds score of 6.27 in favor of linkage of PDA to a 3-centimorgan interval of chromosome 12q24, with 53% of kindreds linked. These findings together establish a recessive component to PDA and implicate a single locus, PDA1, in one third or more of all PDA cases in Iran; they further suggest a role for this locus in PDA worldwide. Finally, these results suggest a general approach to the identification of recessive contributions to sporadic diseases.
许多散发性疾病的病因尚不清楚;外显率降低的隐性基因座的作用是一种难以探究的可能性。我们描述了一种解决此问题的方法,首先在近亲结婚率高的人群中寻找患病率较高的疾病,然后确定在这类人群中,疾病病例是否比对照更常见于近亲结婚的产物,随后对近亲结婚病例进行遗传连锁分析。我们通过对伊朗先天性心脏病的调查证明了这种方法的实用性。我们发现,动脉导管未闭(PDA),一种常见的先天性心脏病,在伊朗先天性心脏病中所占比例(15%)高于美国(2 - 7%)。此外,与伊朗普通人群(25%)或法洛四联症对照病例(30%)相比,伊朗PDA病例的父母近亲结婚率显著增加(63%)。PDA在兄弟姐妹中的复发率为5%。对21例无亲缘关系的近亲结婚PDA病例进行全基因组连锁分析,结果显示多点对数优势评分为6.27,支持PDA与12号染色体q24区域3厘摩区间连锁,53%的家系存在连锁。这些发现共同确定了PDA的隐性成分,并表明在伊朗三分之一或更多的PDA病例中存在一个单一基因座PDA1;它们进一步提示该基因座在全球PDA中的作用。最后,这些结果提示了一种识别散发性疾病隐性因素的通用方法。