Impact of the sex of first child on the prognosis in secondary recurrent miscarriage

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Impact of the sex of first child on the prognosis in secondary recurrent miscarriage. / Christiansen, O B; Pedersen, B; Nielsen, H S; Andersen, Anne-Marie Nybo.

In: Human Reproduction, Vol. 19, No. 12, 2004, p. 2946-2951.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Christiansen, OB, Pedersen, B, Nielsen, HS & Andersen, A-MN 2004, 'Impact of the sex of first child on the prognosis in secondary recurrent miscarriage', Human Reproduction, vol. 19, no. 12, pp. 2946-2951. https://doi.org/10.1093/humrep/deh516

APA

Christiansen, O. B., Pedersen, B., Nielsen, H. S., & Andersen, A-M. N. (2004). Impact of the sex of first child on the prognosis in secondary recurrent miscarriage. Human Reproduction, 19(12), 2946-2951. https://doi.org/10.1093/humrep/deh516

Vancouver

Christiansen OB, Pedersen B, Nielsen HS, Andersen A-MN. Impact of the sex of first child on the prognosis in secondary recurrent miscarriage. Human Reproduction. 2004;19(12):2946-2951. https://doi.org/10.1093/humrep/deh516

Author

Christiansen, O B ; Pedersen, B ; Nielsen, H S ; Andersen, Anne-Marie Nybo. / Impact of the sex of first child on the prognosis in secondary recurrent miscarriage. In: Human Reproduction. 2004 ; Vol. 19, No. 12. pp. 2946-2951.

Bibtex

@article{28bf0d309f0011df928f000ea68e967b,
title = "Impact of the sex of first child on the prognosis in secondary recurrent miscarriage",
abstract = "BACKGROUND: The carriage of a male fetus often initiates maternal immunological reactions against male-specific minor histocompatibility (HY) antigens, which, in theory, could result in subsequent recurrent miscarriage (RM). METHODS: Information about subsequent pregnancy outcome was procured among 182 women with RM after a birth (secondary RM) referred since 1986 using questionnaires, telephone interviews and registers. RESULTS: Significantly more of the women had had a male first-born as compared with a female first-born (110 versus 72; P < 0.02). By January 2002, 58% of those who had a male first-born had given birth to a second live infant compared with 76% of those who previously had had a female first-born (P = 0.01). Women in the former group had a significantly lower chance of having a second child than those in the latter (adjusted hazard ratio 0.59; 95% confidence interval 0.41-0.86). The number of miscarriages after admission and the risk of secondary infertility were significantly greater in women with a male first-born than among those with a female first-born (P < 0.001 and P = 0.02; respectively). CONCLUSIONS: A male first-born seems to be associated with a less favourable reproductive potential among women with secondary RM. Maternal immunization against HY antigens may be responsible for these findings.",
author = "Christiansen, {O B} and B Pedersen and Nielsen, {H S} and Andersen, {Anne-Marie Nybo}",
year = "2004",
doi = "10.1093/humrep/deh516",
language = "English",
volume = "19",
pages = "2946--2951",
journal = "Human Reproduction",
issn = "0268-1161",
publisher = "Oxford Academic",
number = "12",

}

RIS

TY - JOUR

T1 - Impact of the sex of first child on the prognosis in secondary recurrent miscarriage

AU - Christiansen, O B

AU - Pedersen, B

AU - Nielsen, H S

AU - Andersen, Anne-Marie Nybo

PY - 2004

Y1 - 2004

N2 - BACKGROUND: The carriage of a male fetus often initiates maternal immunological reactions against male-specific minor histocompatibility (HY) antigens, which, in theory, could result in subsequent recurrent miscarriage (RM). METHODS: Information about subsequent pregnancy outcome was procured among 182 women with RM after a birth (secondary RM) referred since 1986 using questionnaires, telephone interviews and registers. RESULTS: Significantly more of the women had had a male first-born as compared with a female first-born (110 versus 72; P < 0.02). By January 2002, 58% of those who had a male first-born had given birth to a second live infant compared with 76% of those who previously had had a female first-born (P = 0.01). Women in the former group had a significantly lower chance of having a second child than those in the latter (adjusted hazard ratio 0.59; 95% confidence interval 0.41-0.86). The number of miscarriages after admission and the risk of secondary infertility were significantly greater in women with a male first-born than among those with a female first-born (P < 0.001 and P = 0.02; respectively). CONCLUSIONS: A male first-born seems to be associated with a less favourable reproductive potential among women with secondary RM. Maternal immunization against HY antigens may be responsible for these findings.

AB - BACKGROUND: The carriage of a male fetus often initiates maternal immunological reactions against male-specific minor histocompatibility (HY) antigens, which, in theory, could result in subsequent recurrent miscarriage (RM). METHODS: Information about subsequent pregnancy outcome was procured among 182 women with RM after a birth (secondary RM) referred since 1986 using questionnaires, telephone interviews and registers. RESULTS: Significantly more of the women had had a male first-born as compared with a female first-born (110 versus 72; P < 0.02). By January 2002, 58% of those who had a male first-born had given birth to a second live infant compared with 76% of those who previously had had a female first-born (P = 0.01). Women in the former group had a significantly lower chance of having a second child than those in the latter (adjusted hazard ratio 0.59; 95% confidence interval 0.41-0.86). The number of miscarriages after admission and the risk of secondary infertility were significantly greater in women with a male first-born than among those with a female first-born (P < 0.001 and P = 0.02; respectively). CONCLUSIONS: A male first-born seems to be associated with a less favourable reproductive potential among women with secondary RM. Maternal immunization against HY antigens may be responsible for these findings.

U2 - 10.1093/humrep/deh516

DO - 10.1093/humrep/deh516

M3 - Journal article

C2 - 15513982

VL - 19

SP - 2946

EP - 2951

JO - Human Reproduction

JF - Human Reproduction

SN - 0268-1161

IS - 12

ER -

ID: 21161943