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Pregnancy outcome associated with natural family planning (NFP): scientific basis and experimental design for an international cohort study

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Advances in Contraception

Abstract

Although natural family planning (NFP) is a form of contraception without ostensible maternal risks (other than pregnancy), potential fetal risks could exist if aging gametes are involved in inadvertent fertilization. In the following report, we first review animal studies firmly establishing that aging sperm and aging oocytes (delayed fertilization) cause chromosomal abnormalities in mammals and other species. We next review human studies associating decreased coital frequency with trisomy and studies of NFP populations that generally show no increased frequency of anomalous offspring or spontaneous abortions. Our rationale for initiating an international cohort study is presented, along with the experimental design selected. Preliminary findings indicate that the experimental design chosen will indeed provide information allowing NFP safety to be assessed definitively.

Resumé

Bien que le planning familial naturel (PFN-NFP) soit une forme de contraception ne présentant pas de risques manifestes pour la mère (autres qu'une grossesse), il pourrait y avoir des risques potentiels pour le foetus si des gamètes âgés sont par inadvertance fécondés. Nous passons en revue tout d'abord des études effectuées sur des animaux, établissant fermement que le sperme veillissant et les oocytes vieillissants (fécondation retardée) provoquent des anomalies chromosomales chez les mammifères et d'autres espèces. Nous examinons ensuite des études sur des humains, qui associent diminution coitale et trisomie, et des études de populations pratiquant le PFN, qui ne révèlent généralement pas de fréquence accrue d'enfants anormaux ou d'avortements spontanés. Cette communication expose la raison pour laquelle nous avons entrepris une étude sur une cohorte internationale, ainsi que le concept d'expérimentation que nous avons choisi. Les constatations préliminaires indiquent que ce concept fournira véritablement des informations qui permettront d'évaluer de façon définitive la sécurité du PFN.

Resumen

Aunque la planificación familiar natural (PFN) es una forma de anticoncepción sin riesgos maternos ostensibles, (fuera del embarzo) podrían existir posibles riesgos fetales di gametos que están envejeciendo son inadvertidamente fertilizados. La primera revisión de estudios en animales establece firmemente que espermatozoides y oocytos en envejecimiento (fertilización tardía), causan anormalidades cromosómicas en mamíferos y otras especies. A continuación revisamos estudios en humanos que asocian la disminución de la frecuencia coital con trisomía, y estudios de poblaciones practicando PFN que generalmente no muestran aumento en la frecuencia de descendientes anormales o de abortos espontáneos. Presentamos nuestras razones para iniciar el estudio de una cohorte internactional ademas del diseño experimental elegido proveerá información alegando que la inocuidad de la PFN sea definitivamente valorada.

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References

  1. SimpsonJ.L. (1985). Relationship between congenital anomalies and contraception.Adv. Contracept.,1, 3–30

    PubMed  Google Scholar 

  2. SimpsonJ.L. (1984). Mutagenicity and teratogenicity of injectable and implantable progestins: probable lack of effect. In: G.I.Zatuchni, A.Goldsmith, J.D.Shelton, J.J.Sciarra, eds.,Long Acting Contraception Delivery Systems, Lippincott, Philadelphia, pp. 334–361

    Google Scholar 

  3. World Health Organization (1981). The effect of female sex hormones on fetal development and infant health. World Health Organization (WHO) Technical Report Series 657. WHO, Geneva

    Google Scholar 

  4. SimpsonJ.L. (1978). Genetic consequences of aging sperm or aging ova: animal studies and relevance to humans. In: J.J.Sciarra, G.I.Zatuchni, J.J.Speidel, eds.,Risks, Benefits and Controversies in Fertility Control, Harper and Row, Hagerstown, pp. 506–517

    Google Scholar 

  5. GrayR.H. and KambicR.T. (1988). Epidemiological studies of natural family planning.Hum. Reprod.,3, 693–698

    PubMed  Google Scholar 

  6. Kambic, R., Gray, R.H. and Simpson, J.L. (1988). Aged gametes and NFP: What is currently known.Inter. Rev. NFP, (In press)

  7. BishopM.W.H. (1970). Aging and reproduction in the male.J. Reprod. Fertil. (suppl.),12, 65–87

    Google Scholar 

  8. MarvinT. and Lutwak-MannC. (1975). Biochemical aspects of aging in spermatozoa in relation to motility and fertilizing abilities. In: R.J.Blandau, ed.,Aging Gametes, Their Biology and Pathology, Basel, S. Karger, pp. 122–150

    Google Scholar 

  9. YoungW.C. (1929). A study of function of the epididymis.J. Morphol. Physiol.,47, 479–495

    Google Scholar 

  10. TeshJ.M. and GloverT.D. (1969). Aging of the rabbit spermatozoa in the male tract and its effect on fertility.J. Reprod. Fertil.,20, 287–297

    PubMed  Google Scholar 

  11. Martin-DeLeonP.A., ShaverE.L. and GammalE.B. (1973). Chromosome abnormalities in rabbit blastocytes resulting from spermatozoa aged in the male tract.Fertil. Steril.,24, 212–219

    PubMed  Google Scholar 

  12. ShaverE.L. and Martin-DeLeonP.A. (1975). Effects of aging of sperm in the female and male reproductive tracts before fertilization on the chromosome complement of the blastocytes. In: R.J.Blandau, ed.,Aging Gametes, Their Biology and Pathology, Basel, S. Karger, pp. 151–165

    Google Scholar 

  13. Martin-DeLeonP.A. and ShaverE.L. (1979). Aging of spermatozoa and its effects on karyological abnormalities of resulting conceptuses. In, T.V.N.Persaud, ed.,Advances in the Study of Birth Defects. Vol.3, Lancaster, Baltimore, University Park Press, pp. 1–13

    Google Scholar 

  14. Martin-DeLeonP.A. and BoiceM.L. (1982). Sperm aging in the male and cytogenetic anomalies. An animal model.Hum. Genet.,62, 70–77

    PubMed  Google Scholar 

  15. Martin-DeLeonP.A. and BoiceM.L. (1985). Sperm aging in the male after sexual rest: contribution to chromosome anomalies.Gamete Res.,12, 151–163

    Google Scholar 

  16. SoderwallA.L. and BlandauR.J. (1941). The duration of fertilizing capacity of spermatozoa in the female genital tract of the rat.J. Exp. Zool.,88, 55–64

    Google Scholar 

  17. SoderwallA.L. and YoungW.C. (1940). The effect of aging in the female genital tract on the fertilizing capacity of guinea pig spermatozoa.Anat. Rec.,78, 19–29

    Google Scholar 

  18. TeshJ.M. (1969). Effects of the aging of rabbit spermatozoa in utero on fertilization and prenatal development.J. Reprod. Fertil.,20, 299–306

    PubMed  Google Scholar 

  19. Martin-DeLeonP.A. and ShaverE.L. (1972). Sperm aging in utero and chromosomal anomalies in rabbit blastocytes.Dev. Biol.,28, 480–486

    PubMed  Google Scholar 

  20. Martin-DeLeonP.A. and WilliamsM.B. (1987). Sexual behavior and Down syndrome: the biological mechanism.Am. J. Med. Genet.,27, 693–700

    PubMed  Google Scholar 

  21. Eichenlaub-RitterU., ChandleyA.C. and GosdenR.G. (1986). Alterations to the microtubular cytoskeleton and increased disorder of chromosome alignment in spontaneously ovulated mouse oocytes aged in vivo: an immunofluorescence study.Chromosoma,94, 337–345

    PubMed  Google Scholar 

  22. Eichenlaub-RitterU., ChandleyA.C. and GosdenR.G. (1988). The CBA mouse as a model for age-related aneuploidy in man: studies of oocyte maturation, spindle formation and chromosome alignment during meiosis.Chromosoma,96, 220–226

    PubMed  Google Scholar 

  23. WitschiE. (1952). Overripeness of the egg as a cause of twinning and teratogenesis: A review.Cancer Res.,12, 763–786

    PubMed  Google Scholar 

  24. WitschiE. and LaguensR. (1963). Chromosomal aberrations in embryos from overripe eggs.Dev. Biol.,7, 605–616

    PubMed  Google Scholar 

  25. VickersA.D. (1969). Delayed fertilization and chromosomal anomalies in mouse embryos.J. Reprod. Fertil.,20, 69–76

    PubMed  Google Scholar 

  26. DonahueR.P. (1975). Normal and abnormal chromosomal behavior in the meiotic divisions of mammalian oocytes. In: R.J.Blandau, ed.,Aging Gametes, Their Biology and Pathology, Basel, S. Karger, pp. 50–71

    Google Scholar 

  27. Donahue, R.P. and Karp, L. (1973). Chromosomal anomalies after fertilization of aged, postovulatory mouse oocytes.Am. J. Hum. Genet.,25, 24a

    Google Scholar 

  28. YoungW.C. and BlandauR.J. (1936). Ovum age and the course of gestation in the guinea pig.Science,84, 270

    Google Scholar 

  29. HancockJ.L. (1958). Polyspermy of pig ova.Vet. Rec.,70, 1200

    Google Scholar 

  30. ThibaultC. (1959). Analyse de la fecondation de l'oeuf de la truie apres accomplement ou insemination artificielle.Ann. Inst. Natl. Agron. Serv. D. Ann. Zootech. (Suppl),8, 165–177

    Google Scholar 

  31. ShaverE.L. and CarrD.H. (1969). The chromosome complement of rabbit blastocytes in relation to the time of mating and ovulation.Can. J. Genet. Cytol.,11, 287–293

    PubMed  Google Scholar 

  32. AustinC.R. (1967). Chromosome deterioration in ageing eggs of the rabbit.Nature (London),213, 1018–1019

    Google Scholar 

  33. BlandauR.J. and JordanE.S. (1951). The effect of delayed fertilization on the development of the rat ovum.Am. J. Anat.,68, 275–287

    Google Scholar 

  34. BlandauR.J. (1952). The female factor in fertility and infertility. I. The effects of delayed fertilization on the development of the pronuclei in rat ova.Fertil. Steril.,3, 349–365

    PubMed  Google Scholar 

  35. GermanJ. (1968). Mongolism, delayed fertilization and human sexual behavior.Nature (London),217, 516–518

    Google Scholar 

  36. KinseyA.C., PomeroyW.B., MartinC.E. and GebhardP.H. (1953).Sexual Behavior in the Human Female. Saunders, New York

    Google Scholar 

  37. PenroseL.S. and BergJ.M. (1968). Mongolism and duration of marriage.Nature (London),218, 300

    Google Scholar 

  38. SeverJ.I., GilkesonM.R., ChenT.C., LeyA.C. and EdmondsD. (1970). Epidemiology of mongolism in the collaborative project.Ann. N.Y. Acad. Sci.,171, 328

    Google Scholar 

  39. JubergR.C., GoshenC.R. and SholteF.G. (1973). Socioeconomic and reproductive characteristics of the parents of patients with G1 trisomy syndrome.Soc. Biol.,20, 404–415

    PubMed  Google Scholar 

  40. ShokeirM. (1968). Coital frequency and Down syndrome.Lancet,2, 1081

    Google Scholar 

  41. JamesW.H. (1968). Mongolism, delayed fertilization and sexual behavior.Nature (London),219, 279–280

    Google Scholar 

  42. Milstein-Moscati, I.M. and Becak, W. (1978). Down syndrome and frequency of intercourse.Lancet,629

  43. Milstein-MoscatiI.M. and BecakW. (1981). Occurrence of Down syndrome and human sexual behavior.Am. J. Med. Genet.,9, 211–217

    PubMed  Google Scholar 

  44. JamesW.H. (1983). Parental coital rates and Down syndrome.Am. J. Med. Genet.,14, 783–784

    PubMed  Google Scholar 

  45. JubergR.C. (1983). Origin of chromosome abnormalities: Evidence for delayed fertilization in meiotic nondisfunction.Hum. Genet.,64, 122–127

    PubMed  Google Scholar 

  46. HarplapS., ShinoP.H., RamcharanS., GolbusM., BachmanR., MarnJ. and LewisJ.P. (1985). Chromosomal abnormalities in the Kaiser-Permanante Birth Defect Study, with special reference to contraceptive use around the time of conception.Teratology,31, 381–387

    PubMed  Google Scholar 

  47. BrackenM.B. and VitaK. (1983). Frequency of nonhormonal contraception around conception and association with congenital malformations in offspring.Am. J. Epidemiol.,117, 281–291

    PubMed  Google Scholar 

  48. HassoldT.J. and JacobsP.A. (1984). Trisomy in man.Adv. Hum. Genet.,18, 69–97

    Google Scholar 

  49. SimpsonJ.L. and MillsJ.L. (1985). Methodologic problems in determining fetal loss rates, relevance to chorionic villi sampling. In: M.Fraccaro, G.Simoni, B.Brambati, eds.,First Trimester Fetal Diagnosis, Springer-Verlag, Berlin-Heidelberg, pp. 321–333

    Google Scholar 

  50. MarshallJ. (1968). Congenital defects and the age of spermatozoa.Int. J. Fertil.,134, 110–120

    Google Scholar 

  51. GuerreroV. and RojasO.I. (1975). Spontaneous abortion and aging of human ova and spermatozoa.N. Engl. J. Med.,293, 573–575

    PubMed  Google Scholar 

  52. World Health Organization (1984). A prospective multicenter study of the ovulation method of natural family planning. IV. The outcome of pregnancy.Fertil. Steril.,41, 593–598

    Google Scholar 

  53. Roetzer, J. (1988). Natural family planning and pregnancy outcome.Int. J. Fertil., (In press)

  54. FranceJ.T., GrahamF.M., GaslingL. and HairP.I. (1984). A prospective study of preselection of the sex of offspring by timing intercourse relative to ovulation.Fertil. Steril.,41, 894–900

    PubMed  Google Scholar 

  55. GrayR., KambicR., BicegoG., PerezA., EgerA. and DomenichiniV. (1985). Outcome of pregnancy.Fertil. Steril.,44, 554–555

    PubMed  Google Scholar 

  56. BouéJ., BouéA. and LazarP. (1975). Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions.Teratology,12, 11–26

    PubMed  Google Scholar 

  57. Lazar, P., Gueguen, S., Boué, J. and Boué, A. (1971). In: Boué, A, Thibault, C., eds.,Colleque les Accidents Chromosomi ques de la reproduction, Central Internationale de l'Entrance, Paris

  58. KuhrM.D. (1977). Neural tube defects and midcycle abstinence: A test of the overripeness hypothesis in man.Dev. Med. Child Neurol.,19, 589–592

    PubMed  Google Scholar 

  59. JongbloetP.H. (1971).Mental and Physical Handicaps in Connection with Overripeness Ovopathy, Leiden, Stenfert Kroese

    Google Scholar 

  60. JongbloetP.H. and ZwetsJ.H.Jr. (1976). Pre-ovulatory overripeness of the egg in the human subject.Int. J. Gynaecol. Obstet.,14, 111–116

    PubMed  Google Scholar 

  61. JongbloetP.H. and VonErkelens-ZvetsJ.H.U. (1978). Rhythm methods: Are there risks to the progeny. In: J.J.Sciarra, G.Zatuchni, J.J.Spiedel, eds.,Risks, Benefits and Controversies in Fertility Control, Hagerstown, MD, Harper and Row, pp. 520–533

    Google Scholar 

  62. Kambic, R.T. and Gray, R.H. (1989). Interobserver variation in estimation of day of conception using natural family planning.Fertil. Steril., In press

  63. MillsJ.L., KnoppR.H., SimpsonJ.L., Jovanovic-PetersonL., MetgzerB.E., HolmesL.B., AaronsJ.H., BrownZ., ReedG.F., BieberF.R., VanAllenM., HolzmanI., OberC., PetersonC.M., WithiamM.J., DucklesA., Mueller-HeubackE. and PolkB.F., and National Institute of Child Health and Human Development. (1988). Lack of relation of increased malformation rates in infants of diabetic mothers to glycemic control during organogenesis.N. Engl. J. Med.,318, 671–676

    PubMed  Google Scholar 

  64. SimpsonJ.L., MillsJ.L., HolmesL.B., OberC.L., AaronsJ., JovanovicL. and KnoppR.H. (1987). Low fetal loss rates after ultrasound-proved viability in early pregnancy.J. Am. Med. Assoc.,258, 2555–2557

    Google Scholar 

  65. GuerneriS., BettiioD., SimoniG., BrambatiB., LanzaniA. and FraccaroM. (1987). Prevalence and distribution of chromosome abnormalities in a sample of first trimester interval abortions.Hum. Reprod.,2, 735–739

    PubMed  Google Scholar 

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Simpson, J.L., Gray, R.H., Queenan, J.T. et al. Pregnancy outcome associated with natural family planning (NFP): scientific basis and experimental design for an international cohort study. Adv Contracept 4, 247–264 (1988). https://doi.org/10.1007/BF01849266

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