Presence of fetal DNA in maternal plasma decades after pregnancy

被引:62
作者
Invernizzi, P
Biondi, ML
Battezzati, PM
Perego, F
Selmi, C
Cecchini, F
Podda, M
Simoni, G
机构
[1] Univ Milan, Dept Med Surg & Dent, Div Internal Med, Sch Med, I-20142 Milan, Italy
[2] Univ Milan, Biochem Lab, Dept Med & Surg Dent, San Paolo Sch Med, Milan, Italy
[3] Univ Milan, San Paolo Sch Med, Lab Human Genet, Dept Med Surg & Dent, Milan, Italy
关键词
D O I
10.1007/s00439-002-0725-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cells of fetal origin and cell-free fetal DNA can be detected in the maternal circulation during pregnancy, and it has recently been shown that fetal cells can persist long after delivery. Given the various biological and clinical implications of this fact, we tested the hypothesis that cell-free fetal DNA can be present in maternal plasma decades after pregnancy. We extracted DNA from plasma samples and nucleated blood cells of 160 healthy women with male offspring at different time intervals after delivery (range 1-60 years). All of the samples were tested by means of a real-time quantitative PCR assay for a specific Y chromosome sequence (the SRY gene). Y chromosome-specific DNA was detected in 16 peripheral blood cell samples (10%) and 35 plasma samples (22%). The women with male sequences in the cell fraction had significantly greater total parity (P = 0.018). The proportion of women with detectable Y sequences in the plasma or cell samples was not related to the time since delivery. The fetal DNA concentrations in the genomic material extracted from plasma samples were significantly higher than those extracted from the Y-positive cell samples (149 +/- 140 vs 20 +/- 13 genome-equivalents/ml; P < 0.001). There was no relationship between the concentration of fetal DNA and the time since delivery. Not only fetal cells, but also fragments of fetal DNA can be present in the maternal circulation indefinitely after pregnancy. This finding has practical implications for non-invasive prenatal diagnoses based on maternal blood, and may be considered for possible pathophysiological correlations.
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页码:587 / 591
页数:5
相关论文
共 30 条
  • [1] Altman DG, 1990, PRACTICAL STAT MED R
  • [2] Artlett CM, 2000, ARTHRITIS RHEUM-US, V43, P1062, DOI 10.1002/1529-0131(200005)43:5<1062::AID-ANR16>3.0.CO
  • [3] 2-P
  • [4] Identification of fetal DNA and cells in skin lesions from women with systemic sclerosis
    Artlett, CM
    Smith, JB
    Jimenez, SA
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (17) : 1186 - 1191
  • [5] Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum
    Bianchi, DW
    Zickwolf, GK
    Weil, GJ
    Sylvester, S
    DeMaria, MA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (02) : 705 - 708
  • [6] Fetal cells in the mother: from genetic diagnosis to diseases associated with fetal cell microchimerism
    Bianchi, DW
    [J]. EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2000, 92 (01): : 103 - 108
  • [7] CAMASCHELLA C, 1990, BLOOD, V75, P2102
  • [8] Chen XQ, 1996, NAT MED, V2, P1033
  • [9] Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
    Cheung, MC
    Goldberg, JD
    Kan, YW
    [J]. NATURE GENETICS, 1996, 14 (03) : 264 - 268
  • [10] Chiu RWK, 2001, CLIN CHEM, V47, P1607