Maternal and fetal human leukocyte antigen class Ia and II alleles in severe preeclampsia and eclampsia

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Maternal and fetal human leukocyte antigen class Ia and II alleles in severe preeclampsia and eclampsia. / Emmery, J.; Hachmon, R.; Pyo, C. W.; Nelson, W. C.; Geraghty, D. E.; Andersen, A. M. N.; Melbye, M.; Hviid, T. V. F.

In: Genes and Immunity, Vol. 17, No. 4, 06.2016, p. 251-260.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Emmery, J, Hachmon, R, Pyo, CW, Nelson, WC, Geraghty, DE, Andersen, AMN, Melbye, M & Hviid, TVF 2016, 'Maternal and fetal human leukocyte antigen class Ia and II alleles in severe preeclampsia and eclampsia', Genes and Immunity, vol. 17, no. 4, pp. 251-260. https://doi.org/10.1038/gene.2016.20

APA

Emmery, J., Hachmon, R., Pyo, C. W., Nelson, W. C., Geraghty, D. E., Andersen, A. M. N., Melbye, M., & Hviid, T. V. F. (2016). Maternal and fetal human leukocyte antigen class Ia and II alleles in severe preeclampsia and eclampsia. Genes and Immunity, 17(4), 251-260. https://doi.org/10.1038/gene.2016.20

Vancouver

Emmery J, Hachmon R, Pyo CW, Nelson WC, Geraghty DE, Andersen AMN et al. Maternal and fetal human leukocyte antigen class Ia and II alleles in severe preeclampsia and eclampsia. Genes and Immunity. 2016 Jun;17(4):251-260. https://doi.org/10.1038/gene.2016.20

Author

Emmery, J. ; Hachmon, R. ; Pyo, C. W. ; Nelson, W. C. ; Geraghty, D. E. ; Andersen, A. M. N. ; Melbye, M. ; Hviid, T. V. F. / Maternal and fetal human leukocyte antigen class Ia and II alleles in severe preeclampsia and eclampsia. In: Genes and Immunity. 2016 ; Vol. 17, No. 4. pp. 251-260.

Bibtex

@article{cdcc01382cdc47b1a9b39600761a84a7,
title = "Maternal and fetal human leukocyte antigen class Ia and II alleles in severe preeclampsia and eclampsia",
abstract = "A line of investigations indicate that genes in the human leukocyte antigen (HLA) complex are involved in a successful acceptance of the semiallogeneic fetus during pregnancy. In this study, associations between specific HLA class Ia (HLA-A and -B) and class II (HLA-DRB1, -DQA1, -DQB1, -DPA1 and -DPB1) alleles and the risk of developing severe preeclampsia/eclampsia were investigated in a detailed and large-scale study. In total, 259 women diagnosed with severe preeclampsia or eclampsia and 260 matched control women with no preeclampsia, together with their neonates, were included in the study. HLA genotyping for mothers and neonates was performed using next-generation sequencing. The HLA-DPB1*04:01:01G allele was significantly more frequent (Pc=0.044) among women diagnosed with severe preeclampsia/eclampsia compared with controls, and the DQA1*01:02:01G allele frequency was significantly lower (Pc=0.042) among newborns born by women with severe preeclampsia/eclampsia compared with controls. In mothers with severe preeclampsia/eclampsia, homozygosity was significantly more common compared with controls at the HLA-DPB1 locus (Pc=0.0028). Although the current large study shows some positive results, more studies, also with a functional focus, are needed to further clarify a possible role of the classical HLA genes in preeclampsia.",
author = "J. Emmery and R. Hachmon and Pyo, {C. W.} and Nelson, {W. C.} and Geraghty, {D. E.} and Andersen, {A. M. N.} and M. Melbye and Hviid, {T. V. F.}",
year = "2016",
month = jun,
doi = "10.1038/gene.2016.20",
language = "English",
volume = "17",
pages = "251--260",
journal = "Genes and Immunity",
issn = "1466-4879",
publisher = "nature publishing group",
number = "4",

}

RIS

TY - JOUR

T1 - Maternal and fetal human leukocyte antigen class Ia and II alleles in severe preeclampsia and eclampsia

AU - Emmery, J.

AU - Hachmon, R.

AU - Pyo, C. W.

AU - Nelson, W. C.

AU - Geraghty, D. E.

AU - Andersen, A. M. N.

AU - Melbye, M.

AU - Hviid, T. V. F.

PY - 2016/6

Y1 - 2016/6

N2 - A line of investigations indicate that genes in the human leukocyte antigen (HLA) complex are involved in a successful acceptance of the semiallogeneic fetus during pregnancy. In this study, associations between specific HLA class Ia (HLA-A and -B) and class II (HLA-DRB1, -DQA1, -DQB1, -DPA1 and -DPB1) alleles and the risk of developing severe preeclampsia/eclampsia were investigated in a detailed and large-scale study. In total, 259 women diagnosed with severe preeclampsia or eclampsia and 260 matched control women with no preeclampsia, together with their neonates, were included in the study. HLA genotyping for mothers and neonates was performed using next-generation sequencing. The HLA-DPB1*04:01:01G allele was significantly more frequent (Pc=0.044) among women diagnosed with severe preeclampsia/eclampsia compared with controls, and the DQA1*01:02:01G allele frequency was significantly lower (Pc=0.042) among newborns born by women with severe preeclampsia/eclampsia compared with controls. In mothers with severe preeclampsia/eclampsia, homozygosity was significantly more common compared with controls at the HLA-DPB1 locus (Pc=0.0028). Although the current large study shows some positive results, more studies, also with a functional focus, are needed to further clarify a possible role of the classical HLA genes in preeclampsia.

AB - A line of investigations indicate that genes in the human leukocyte antigen (HLA) complex are involved in a successful acceptance of the semiallogeneic fetus during pregnancy. In this study, associations between specific HLA class Ia (HLA-A and -B) and class II (HLA-DRB1, -DQA1, -DQB1, -DPA1 and -DPB1) alleles and the risk of developing severe preeclampsia/eclampsia were investigated in a detailed and large-scale study. In total, 259 women diagnosed with severe preeclampsia or eclampsia and 260 matched control women with no preeclampsia, together with their neonates, were included in the study. HLA genotyping for mothers and neonates was performed using next-generation sequencing. The HLA-DPB1*04:01:01G allele was significantly more frequent (Pc=0.044) among women diagnosed with severe preeclampsia/eclampsia compared with controls, and the DQA1*01:02:01G allele frequency was significantly lower (Pc=0.042) among newborns born by women with severe preeclampsia/eclampsia compared with controls. In mothers with severe preeclampsia/eclampsia, homozygosity was significantly more common compared with controls at the HLA-DPB1 locus (Pc=0.0028). Although the current large study shows some positive results, more studies, also with a functional focus, are needed to further clarify a possible role of the classical HLA genes in preeclampsia.

U2 - 10.1038/gene.2016.20

DO - 10.1038/gene.2016.20

M3 - Journal article

C2 - 27121092

VL - 17

SP - 251

EP - 260

JO - Genes and Immunity

JF - Genes and Immunity

SN - 1466-4879

IS - 4

ER -

ID: 163126541