TY - JOUR
T1 - Interpregnancy and interbirth intervals and all-cause, cardiovascular-related and cancer-related maternal mortality
T2 - Findings from a large population-based cohort study
AU - Weisband, Yiska Loewenberg
AU - Manor, Orly
AU - Friedlander, Yechiel
AU - Hochner, Hagit
AU - Paltiel, Ora
AU - Calderon-Margalit, Ronit
N1 - Publisher Copyright:
© 2020 Author(s).
PY - 2020/11
Y1 - 2020/11
N2 - Introduction Scarce research is available regarding the association between interbirth intervals (IBI) and long-term maternal health outcomes, particularly cardiovascular disease (CVD) mortality. We aimed to assess whether IBIs were associated with all-cause, CVD-related and cancer-related mortality. Methods We conducted a cohort study in the setting of the Jerusalem Perinatal Study. Women with at least two consecutive singleton live births in 1964-1976 (N=18 294) were followed through 2016. IBIs were calculated as the interval between women's first and second cohort birth. We estimated associations between IBIs and mortality using Cox's proportional hazards models, adjusting for age, parity, maternal education, maternal origin and paternal socioeconomic status. Date of last menstrual period was available for a subset of women. We assessed the interpregnancy interval (IPI) for these women and compared the models using IPI and IBI. Results During 868 079 years of follow up (median follow-up: 49.0 years), 3337 women died. Women with IBIs <15 months had higher all-cause mortality rates (HR 1.18; 95% CI 1.05 to 1.33) compared to women with 33-month to 68-month IBIs (reference category). IBI and CVD mortality appeared to have a J-shaped association; IBIs of <15, 15-20, 21-2626-2632, 33-68 and ≥69 months had HRs of 1.44, 1.40, 1.33, 1.14, 1.00 and 1.30, respectively. No substantial association was found with cancer mortality. Models using IPIs and those using IBI were similar. Conclusion Our results support the WHO recommendations for IPIs of ≥24 months and add additional evidence regarding long-term CVD mortality.
AB - Introduction Scarce research is available regarding the association between interbirth intervals (IBI) and long-term maternal health outcomes, particularly cardiovascular disease (CVD) mortality. We aimed to assess whether IBIs were associated with all-cause, CVD-related and cancer-related mortality. Methods We conducted a cohort study in the setting of the Jerusalem Perinatal Study. Women with at least two consecutive singleton live births in 1964-1976 (N=18 294) were followed through 2016. IBIs were calculated as the interval between women's first and second cohort birth. We estimated associations between IBIs and mortality using Cox's proportional hazards models, adjusting for age, parity, maternal education, maternal origin and paternal socioeconomic status. Date of last menstrual period was available for a subset of women. We assessed the interpregnancy interval (IPI) for these women and compared the models using IPI and IBI. Results During 868 079 years of follow up (median follow-up: 49.0 years), 3337 women died. Women with IBIs <15 months had higher all-cause mortality rates (HR 1.18; 95% CI 1.05 to 1.33) compared to women with 33-month to 68-month IBIs (reference category). IBI and CVD mortality appeared to have a J-shaped association; IBIs of <15, 15-20, 21-2626-2632, 33-68 and ≥69 months had HRs of 1.44, 1.40, 1.33, 1.14, 1.00 and 1.30, respectively. No substantial association was found with cancer mortality. Models using IPIs and those using IBI were similar. Conclusion Our results support the WHO recommendations for IPIs of ≥24 months and add additional evidence regarding long-term CVD mortality.
KW - EPIDEMIOLOGY
KW - Lifecourse/ Childhood Circumstances
KW - MATERNAL HEALTH
KW - MIDWIFERY
KW - SOCIAL INEQUALITIES
UR - http://www.scopus.com/inward/record.url?scp=85092749772&partnerID=8YFLogxK
U2 - 10.1136/jech-2020-214242
DO - 10.1136/jech-2020-214242
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C2 - 32655002
AN - SCOPUS:85092749772
SN - 0143-005X
VL - 74
SP - 957
EP - 963
JO - Journal of Epidemiology and Community Health
JF - Journal of Epidemiology and Community Health
IS - 11
ER -