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Is gestation in Prader-Willi syndrome affected by the genetic subtype?

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Abstract

Background

Prader-Willi syndrome (PWS) is a complex genetic disorder with errors in genomic imprinting, generally due to a paternal deletion of chromosome 15q11-q13 region. Maternal disomy 15 (both 15s from the mother) is the second most common form of PWS resulting from a trisomic zygote followed by trisomy rescue in early pregnancy and loss of the paternal chromosome 15. However, trisomy 15 or mosaicism for trisomy 15 may be present in the placenta possibly leading to placental abnormalities affecting gestational age and delivery.

Methods and Subjects

We examined growth and gestational data from 167 PWS infants (93 males and 74 females; 105 infants with 15q11-q13 deletion and 62 infants with maternal disomy 15) to determine if there are differences in gestation between the two genetic subtypes.

Results

No significant differences in growth data (birth weight, length, head circumference) or average gestational ages were found between the two genetic subgroups. However, post-term deliveries (> 42 weeks gestation) were more common in the maternal disomy group (i.e., 12 of 62 infants) compared with the deletion group (i.e., 7 of 105 infants) (chi-square test = 6.22; p < 0.02). The distribution of gestational ages in the 15q11-q13 deletion group was more bell-shaped or normal while the distribution in the maternal disomy group suggested a bimodal pattern.

Conclusions

Maternal disomy 15 in PWS may contribute to disturbances in gestational age and delivery by impacting on placental structure or function secondary to the abnormal chromosomal number in the placental cells or in mechanisms leading to the maternal disomy status in PWS infants.

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References

  1. Bittel DC, Butler MG. Prader-Willi syndrome: Clinical genetics, cytogenetics and molecular biology. Expert Rev Mol Med. 2005;7(14):1–20.

    Article  PubMed  Google Scholar 

  2. Butler MG, Hanchett J, Thompson T. Clinical findings and natural history of Prader-Willi syndrome. In: Butler MG, Lee PDK, Whitman BY, editors. Management of Prader-Willi Syndrome. 3rd ed. Springer-Verlag Publishers: New York; 2006. p. 3–48.

    Google Scholar 

  3. Goldstone AP, Holland AJ, Hauffa BP, Hokken-Koelega AC, Tauber M. Recommendations for the diagnosis and management of Prader-Willi syndrome. J Clin Endocrinol Metab. 2008;93(11):4183–97.

    Article  CAS  PubMed  Google Scholar 

  4. Cassidy SB, Driscoll DJ. Prader-Willi syndrome. Eur J Hum Genet. 2009;17(1):3–13.

    Article  CAS  PubMed  Google Scholar 

  5. Butler MG, Thompson T. Prader-Willi syndrome: Clinical and genetic findings. The Endocrinologist. 2000;10:3S–16S.

    Article  Google Scholar 

  6. Butler MG, Bittel DC, Kibiryeva N, Talebizadeh Z, Thompson T. Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy. Pediatrics. 2004;113(3 Pt 1):565–73.

    Article  PubMed  Google Scholar 

  7. Bittel DC, Kibiryeva N, Butler MG. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome. Pediatrics. 2006;118(4):e1276–1283.

    Article  PubMed  Google Scholar 

  8. Kubota T, Das S, Christian SL, Baylin SB, Herman JG, Ledbetter DH. Methylation-specific PCR simplifies imprinting analysis. Nat Genet. 1997;16(1):16–7.

    CAS  PubMed  Google Scholar 

  9. Glenn CC, Porter KA, Jong MT, Nicholls RD, Driscoll DJ. Functional imprinting and epigenetic modification of the human SNRPN gene. Hum Mol Genet. 1993;2(12):2001–5.

    Article  CAS  PubMed  Google Scholar 

  10. Nicholls RD, Knepper JL. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes. Annu Rev Genomics Hum Genet. 2001;2:153–75.

    Article  CAS  PubMed  Google Scholar 

  11. Cassidy SB, Lai LW, Erickson RP, Magnuson L, Thomas E, Gendron R, et al. Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy. Am J Hum Genet. 1992;51(4):701–8.

    CAS  PubMed  Google Scholar 

  12. Warburton D, Byrne J, Canki N. Trisomy. In: Warburton D, Byrne J, Canki N, editors. Chromosome anomalies and prenatal development: An atlas. New York: Oxford University Press; 1991. p. 57–62.

    Google Scholar 

  13. Christian SL, Smith AC, Macha M, Black SH, Elder FF, Johnson JM, et al. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Prenat Diagn. 1996;16(4):323–32.

    Article  CAS  PubMed  Google Scholar 

  14. Harris A, Collins J, Vetrie D, Cole C, Bobrow M. X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease. J Med Genet. 1992;29(9):608–14.

    Article  CAS  PubMed  Google Scholar 

  15. Sangha KK, Stephenson MD, Brown CJ, Robinson WP. Extremely skewed X-chromosome inactivation is increased in women with recurrent spontaneous abortion. Am J Hum Genet. 1999;65(3):913–7.

    Article  CAS  PubMed  Google Scholar 

  16. Maier EM, Kammerer S, Muntau AC, Wichers M, Braun A, Roscher AA. Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivation. Ann Neurol. 2002;52(5):683–8.

    Article  CAS  PubMed  Google Scholar 

  17. Talebizadeh Z, Bittel DC, Veatch OJ, Kibiryeva N, Butler MG. Brief report: Non-random X chromosome inactivation in females with autism. J Autism Dev Disord. 2005;35(5):675–81.

    Article  CAS  PubMed  Google Scholar 

  18. Migeon BR. Non-random X chromosome inactivation in mammalian cells. Cytogenet Cell Genet. 1998;80(1–4):142–8.

    Article  CAS  PubMed  Google Scholar 

  19. Lau AW, Brown CJ, Penaherrera M, Langlois S, Kalousek DK, Robinson WP. Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism. Am J Hum Genet. 1997;61(6):1353–61.

    Article  CAS  PubMed  Google Scholar 

  20. Krepischi AC, Kok F, Otto PG. X chromosome-inactivation patterns in patients with Rett syndrome. Hum Genet. 1998;102(3):319–21.

    Article  CAS  PubMed  Google Scholar 

  21. Ledbetter DH, Zachary JM, Simpson JL, Golbus MS, Pergament E, Jackson L et al. Cytogenetic results from the U.S. Collaborative Study on CVS. Prenat Diagn. 1992; 12(5):317–45.

    Google Scholar 

  22. Butler MG, Theodoro MF, Bittel DC, Kuipers PJ, Driscoll DJ, Talebizadeh Z. X-chromosome inactivation patterns in females with Prader-Willi syndrome. Am J Med Genet A. 2007;143(5):469–75.

    PubMed  Google Scholar 

  23. Woodage T, Prasad M, Dixon JW, Selby RE, Romain DR, Columbano-Green LM, et al. Bloom syndrome and maternal uniparental disomy for chromosome 15. Am J Hum Genet. 1994;55(1):74–80.

    CAS  PubMed  Google Scholar 

  24. Roback EW, Barakat AJ, Dev VG, Mbikay M, Chretien M, Butler MG. An infant with distal deletion of the long arm of chromosome 15 (q26.1-qter) and loss of insulin-like growth factor 1 receptor gene. Am J Med Genet. 1991; 38:74–9.

    Google Scholar 

  25. Eggermann T. Silver-Russell and Beckwith-Wiedemann syndromes: Opposite (epi)mutations in 11p15 result in opposite clinical pictures. Horm Res. 2009;71:30–5.

    Article  CAS  PubMed  Google Scholar 

  26. Eggermann T, Eggermann K, Schonherr N. Growth retardation versus overgrowth: Silver-Russell syndrome is genetically opposite to Beckwith-Wiedemann syndrome. Trends Genet. 2008;24:195–204.

    Article  CAS  PubMed  Google Scholar 

  27. Bliek J, Verde G, Callaway J, Maas SM, de Crescenzo A, Sparago A, et al. Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome. Eur J Hum Genet. 2009;17:611–9.

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

The authors would like to acknowledge the families with Prader-Willi syndrome. We thank Jasmin Tanaja and Cindy Yoo from University of California-Irvine for data retrieval. This study was partially supported by NIH rare disease grant (1U54RR019478).

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Correspondence to Merlin G. Butler.

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Butler, M.G., Sturich, J., Myers, S.E. et al. Is gestation in Prader-Willi syndrome affected by the genetic subtype?. J Assist Reprod Genet 26, 461–466 (2009). https://doi.org/10.1007/s10815-009-9341-7

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  • DOI: https://doi.org/10.1007/s10815-009-9341-7

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