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Sökning: WFRF:(Karalexi M A) > (2017) > Maternal fetal loss...

Maternal fetal loss history and increased acute leukemia subtype risk in subsequent offspring : a systematic review and meta-analysis

Karalexi, M. A. (författare)
University of Athens
Dessypris, N. (författare)
University of Athens
Skalkidou, Alkistis, 1977- (författare)
Uppsala universitet,Obstetrisk forskning
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Biniaris-Georgallis, S. -I (författare)
University of Athens
Kalogirou, E. I. (författare)
University of Athens
Thomopoulos, T. P. (författare)
University of Athens
Herlenius, E. (författare)
Karolinska Institutet
Spector, L. G. (författare)
University of Minnesota
Loutradis, D. (författare)
University of Athens
Chrousos, G. P. (författare)
University of Athens
Petridou, E. Th. (författare)
University of Athens
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 (creator_code:org_t)
2017-04-11
2017
Engelska.
Ingår i: Cancer Causes and Control. - : SPRINGER. - 0957-5243 .- 1573-7225. ; 28:6, s. 599-624
  • Forskningsöversikt (refereegranskat)
Abstract Ämnesord
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  • Purpose History of fetal loss including miscarriage and stillbirth has been inconsistently associated with childhood (0-14 years) leukemia in subsequent offspring. A quantitative synthesis of the inconclusive literature by leukemia subtype was therefore conducted. Methods Eligible studies (N = 32) were identified through the screening of over 3500 publications. Random-effects meta-analyses were conducted on the association of miscarriage/stillbirth history with overall (AL; 18,868 cases/35,685 controls), acute lymphoblastic (ALL; 16,150 cases/38,655 controls), and myeloid (AML; 3042 cases/32,997 controls) leukemia. Sensitivity and subgroup analyses by age and ALL subtype, as well as meta-regression were undertaken. Results Fetal loss history was associated with increased AL risk [Odds Ratio (OR) 1.10, 95% Confidence Intervals (CI) 1.04-1.18]. The positive association was seen for ALL (OR 1.12, 95%CI 1.05-1.19) and for AML (OR 1.13, 95%CI 0.91-1.41); for the latter the OR increased in sensitivity analyses. Notably, stillbirth history was significantly linked to ALL risk (OR 1.33, 95%CI 1.02-1.74), but not AML. By contrast, the association of ALL and AML with previous miscarriage reached marginal significance. The association of miscarriage history was strongest in infant ALL (OR 2.34, 95%CI 1.19-4.60). Conclusions In this meta-analysis involving > 50,000 children, we found noteworthy associations by indices of fetal loss, age at diagnosis, and leukemia type; namely, of stillbirth with ALL and miscarriage history with infant ALL. Elucidation of plausible underlying mechanisms may provide insight into leukemia pathogenesis and indicate monitoring interventions prior to and during pregnancy.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

Miscarriage
Stillbirth
Childhood acute lymphoblastic leukemia
Childhood acute myeloid leukemia
Meta-analysis
Meta-regression

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