TY - JOUR
T1 - Size at birth, weight gain over the life course, and low-grade inflammation in young adulthood: Northern Finland 1966 birth cohort study
AU - Tzoulaki, Ioanna
AU - Jarvelin, Marjo Riitta
AU - Hartikainen, Anna Liisa
AU - Leinonen, Maija
AU - Pouta, Anneli
AU - Paldanius, Mika
AU - Ruokonen, Aimo
AU - Canoy, Dexter
AU - Sovio, Ulla
AU - Saikku, Pekka
AU - Elliott, Paul
N1 - , Wellcome Trust, United Kingdom
PY - 2008/4
Y1 - 2008/4
N2 - Aims: Low-grade inflammation might mediate associations between size at birth, early life growth, excessive weight gain, and subsequent risk of cardiovascular disease in adult life. Our aim was to investigate relationships between fetal growth, weight over the life course, and low-grade inflammation measured by serum high sensitivity C-reactive protein (CRP) levels at 31 years. Methods and results: General population-based northern Finland 1966 Birth Cohort study of 5840 participants attending a clinical examination at 31 years, including measurement of CRP. Weight and height were assessed at birth, 12 months, and 14 and 31 years of age. CRP levels at 31 years were 16% [95% confidence interval (CI) 8, 23] higher per 1 kg lower birth weight, 21% (95% CI 2, 37) higher per 10 cm lower birth length, and 24% (95% CI 10, 36) higher per 1 kg/m3 lower ponderal index, after adjustment for potential confounders. Participants with highest tertile body mass index (BMI) at 31 years and lowest tertile birth weight had the highest average CRP levels. Per unit increase in BMI from 14 to 31 years was associated with 16% (95% CI 14, 17) higher CRP levels; the association was larger for those in the top BMI tertile at age 14 years. Conclusion: Systemic low-grade inflammation may lie on the causal pathway that relates impaired fetal growth and weight gain from childhood to adulthood to adverse adult cardiovascular health. Lifestyle changes from early life might be an important step in reducing cardiovascular risk in adults. © The Author 2008.
AB - Aims: Low-grade inflammation might mediate associations between size at birth, early life growth, excessive weight gain, and subsequent risk of cardiovascular disease in adult life. Our aim was to investigate relationships between fetal growth, weight over the life course, and low-grade inflammation measured by serum high sensitivity C-reactive protein (CRP) levels at 31 years. Methods and results: General population-based northern Finland 1966 Birth Cohort study of 5840 participants attending a clinical examination at 31 years, including measurement of CRP. Weight and height were assessed at birth, 12 months, and 14 and 31 years of age. CRP levels at 31 years were 16% [95% confidence interval (CI) 8, 23] higher per 1 kg lower birth weight, 21% (95% CI 2, 37) higher per 10 cm lower birth length, and 24% (95% CI 10, 36) higher per 1 kg/m3 lower ponderal index, after adjustment for potential confounders. Participants with highest tertile body mass index (BMI) at 31 years and lowest tertile birth weight had the highest average CRP levels. Per unit increase in BMI from 14 to 31 years was associated with 16% (95% CI 14, 17) higher CRP levels; the association was larger for those in the top BMI tertile at age 14 years. Conclusion: Systemic low-grade inflammation may lie on the causal pathway that relates impaired fetal growth and weight gain from childhood to adulthood to adverse adult cardiovascular health. Lifestyle changes from early life might be an important step in reducing cardiovascular risk in adults. © The Author 2008.
KW - Birth weight
KW - C-reactive protein
KW - Cardiovascular risk factors
KW - Life course epidomiology
KW - Weight gain
U2 - 10.1093/eurheartj/ehn105
DO - 10.1093/eurheartj/ehn105
M3 - Article
C2 - 18403494
SN - 1522-9645
VL - 29
SP - 1049
EP - 1056
JO - European Heart Journal
JF - European Heart Journal
IS - 8
ER -