• Riitta Marttila, Ritva Haataja, Mika Rämet, Marja-Leena Pokela, Outi Tammela, and Mikko Hallman.
• Central Hospital of Southern Ostrobothnia, Seinäjoki, Finland.
• Ann. Med. 2003 Jan 1; 35 (5): 344-52.

BackgroundSurfactant protein A (SP-A) polymorphisms are associated with susceptibility to respiratory distress syndrome (RDS). According to present hypothesis the association between SP-A polymorphisms and RDS may not be applicable to the entire population of premature infants.AimThe present study was designed to evaluate the associations between SP-A allelic variants and RDS in a population consisting of 198 premature twin pairs.MethodGenotype analysis of the SP-A1 and SP-A2 genes and twin zygosity definition were carried out.ResultsThe main SP-A1 allele 6A2 (P = 0.030), genotype 6A2/6A2 (P = 0.0042) and haplotype 6A2-1A(0) (P = 0.016) were over-represented in healthy premature twin infants compared to RDS twins. The homozygous genotype 6A2/6A2 was over-represented in twin pairs of whom both were healthy compared to twins concordant for RDS (odds ratio 0.18, confidence intervals 0.06-0.6, P = 0.0016) and born between 32 and 36 weeks. 6A2/6A2 was also overrepresented in healthy twin pairs with birth weight sum higher than the median (OR 0.15, CI 0.04-0.6, P = 0.0025).ConclusionsIn twins, the association between SP-A polymorphism and RDS is different from that seen in premature singleton infants. The factor associated with SP-A genotype-specific susceptibility to RDS appears to be related to the size of uterus and the length of gestation at birth.

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