Genetics of recurrent pregnancy loss

被引:141
作者
Sierra, Sony [1 ]
Stephenson, Mary [1 ]
机构
[1] Univ Chicago, Dept Obstet & Gynecol, Sect Reprod Endocrinol & Infertil, Chicago, IL 60637 USA
关键词
recurrent pregnancy loss; recurrent miscarriage; cytogenetics; translocations; preimplantation genetic diagnosis;
D O I
10.1055/s-2006-931797
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Recurrent pregnancy loss (RPL) is a devastating reproductive problem affecting approximately 5% of couples trying to conceive. Genetic factors appear to be highly associated with reproductive loss. In this article, genetic factors are reviewed in terms of random numerical chromosome errors in miscarriage specimens and carriers of structural chromosome rearrangements that may result in unbalanced chromosome errors in pregnancies. Recently, research has generated interest in genetic markers for recurrent loss such as skewed X-chromosome inactivation and human leukocyte antigen-G polymorphisms. Assisted reproductive technologies (specifically, preimplantation genetic diagnosis) have been offered to couples with recurrent pregnancy loss; however, more data need to be evaluated before routine use can be advocated. Management of genetic factors in RPL should include therapy based on the highest level of evidence, genetic counseling, and close monitoring of subsequent pregnancies.
引用
收藏
页码:17 / 24
页数:8
相关论文
共 54 条
  • [1] *ACOG COMM PRACT B, 2005, MAN REC EARL PREGN L
  • [2] HLA-G genotypes and pregnancy outcome in couples with unexplained recurrent miscarriage
    Aldrich, CL
    Stephenson, MD
    Karrison, T
    Odem, RR
    Branch, DW
    Scott, JR
    Schreiber, JR
    Ober, C
    [J]. MOLECULAR HUMAN REPRODUCTION, 2001, 7 (12) : 1167 - 1172
  • [3] [Anonymous], 1987, HUM GENET
  • [4] Skewed X-chromosome inactivation is associated with trisomy in women ascertained on the basis of recurrent spontaneous abortion or chromosomally abnormal pregnancies
    Beever, CL
    Stephenson, MD
    Pañaherrera, MS
    Jiang, RH
    Kalousek, DK
    Hayden, M
    Field, L
    Brown, CJ
    Robinson, WP
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (02) : 399 - 407
  • [5] Cytogenetic diagnosis of "normal 46,XX" karyotypes in spontaneous abortions frequently may be misleading
    Bell, KA
    Van Deerlin, PG
    Haddad, BR
    Feinberg, RF
    [J]. FERTILITY AND STERILITY, 1999, 71 (02) : 334 - 341
  • [6] A COLLABORATIVE STUDY OF THE SEGREGATION OF INHERITED CHROMOSOME STRUCTURAL REARRANGEMENTS IN 1356 PRENATAL DIAGNOSES
    BOUE, A
    GALLANO, P
    [J]. PRENATAL DIAGNOSIS, 1984, 4 : 45 - 67
  • [7] RETROSPECTIVE AND PROSPECTIVE EPIDEMIOLOGICAL-STUDIES OF 1500 KARYOTYPED SPONTANEOUS HUMAN ABORTIONS
    BOUE, J
    BOUE, A
    LAZAR, P
    [J]. TERATOLOGY, 1975, 12 (01) : 11 - 26
  • [8] Parental karyotype and subsequent live births in recurrent miscarriage
    Carp, H
    Feldman, B
    Oelsner, G
    Schiff, E
    [J]. FERTILITY AND STERILITY, 2004, 81 (05) : 1296 - 1301
  • [9] Future pregnancy outcome in unexplained recurrent first trimester miscarriage
    Clifford, K
    Rai, R
    Regan, L
    [J]. HUMAN REPRODUCTION, 1997, 12 (02) : 387 - 389
  • [10] Chromosome segregation in a man heterozygous for a pericentric inversion, inv(9)(p11q13), analyzed by using sperm karyotyping and two-color fluorescence in situ hybridization on sperm nuclei
    Colls, P
    Blanco, J
    MartinezPasarell, O
    Vidal, F
    Egozcue, J
    Marquez, C
    Guitart, M
    Templado, C
    [J]. HUMAN GENETICS, 1997, 99 (06) : 761 - 765