Number of parity and the risk of non-Hodgkin lymphomas: a dose-response meta-analysis of observational studies

Hematology. 2017 Jun;22(5):274-285. doi: 10.1080/10245332.2016.1252002. Epub 2016 Nov 10.

Abstract

Background: Epidemiological reports have shown that parity is associated with a risk of developing non-Hodgkin lymphomas (NHL). However, the findings have been inconsistent.

Methods: We searched the EMBASE and PubMed databases for eligible studies up to 10 March 2016. Category and generalized least square regression models were used to perform data analyses.

Results: In total, five cohort and seven case-control studies were identified. Categorical analyses indicated that parity number has little association with NHL and its subtypes. In dose-risk analyses, there were no relationships between parity and NHL risk (pfor association = 0.064; n = 10). The summarized risk ratio (RR) was 0.97 (95% confidence interval (CI): 0.95-1.00; I2 = 57.8%; pheterogeneity = 0.014; Power = 0.79) for each additional live birth increase. Similarly, for B-cell NHL, there was a null association between parity and NHL risk (pfor association = 0.121; n = 5). The combined RR was 0.96 (95% CI = 0.90-1.03; I2 = 63.7%; pheterogeneity = 0.026; Power = 0.71) for each additional live birth. For follicular NHL, there was still a non-significant association identified (pfor association = 0.071; n = 4), the pooled RR was 1.00 (95% CI = 0.95-1.07; I2 = 17.3%; pheterogeneity = 0.305; Power = 0.26) per additional live birth.

Conclusions: Our data identified little evidence suggesting that high parity is a protective factor against the development of NHL, including its B-cell and follicular subtypes.

Keywords: Parity; dose–response; meta-analysis; non-Hodgkin lymphomas.

Publication types

  • Meta-Analysis
  • Review

MeSH terms

  • Female
  • Humans
  • Live Birth*
  • Lymphoma, B-Cell / epidemiology*
  • Lymphoma, Follicular / epidemiology*
  • Parity*
  • Pregnancy
  • Risk Factors