Body mass index at birth and early life and colorectal cancer: A two‐sample Mendelian randomization analysis in European and East Asian genetic similarity populations

Summary Background Varying obesogenic inherited predisposition in early to later life may differentially impact colorectal cancer (CRC) development. Previous Mendelian randomization (MR) studies, conducted in populations of European genetic similarity, have not observed any significant associations...

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Published inPediatric obesity Vol. 20; no. 1; pp. e13186 - n/a
Main Authors Papadimitriou, Nikos, Murphy, Neil, Jenab, Mazda, Chen, Zhishan, Brenner, Hermann, Kweon, Sun‐Seog, Le Marchand, Loic, Moreno, Victor, Platz, Elizabeth A., Duijnhoven, Fränzel J. B., Cheng, Iona, Pai, Rish K., Phipps, Amanda I., Peters, Ulrike, Zheng, Wei, Hughes, David J.
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Inc 01.01.2025
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ISSN2047-6302
2047-6310
DOI10.1111/ijpo.13186

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Abstract Summary Background Varying obesogenic inherited predisposition in early to later life may differentially impact colorectal cancer (CRC) development. Previous Mendelian randomization (MR) studies, conducted in populations of European genetic similarity, have not observed any significant associations between early life body weight with CRC risk. However, it remains unclear whether body mass index (BMI) at different early lifetime points is causally related with CRC risk in both Europeans and East Asian populations. Objectives We conducted a two‐sample MR study to investigate potential causal relationships between genetically predicted BMI during early life (birth to 8 years old) and at specific periods (birth, transient, early rise and late rise) and CRC risk. Methods Summary data were obtained from genome‐wide association study (GWAS) of BMI in 28 681 children from the Norwegian Mother, Father and Child Cohort Study (MoBa) study and applied to CRC GWAS data from European and East Asian descent populations (102 893 cases and 485 083 non‐cases). Results There were no significant associations observed between early life BMI and CRC risk in European or East Asian populations. The effect estimates were similar in European studies (odds ratio [OR] per a 1‐standard deviation [SD] increase: 1.01, 95% confidence interval [CI]: 0.95, 1.07) and in East Asians (OR per a 1‐SD increase: 1.02, 95% CI: 0.91, 1.14). Similar nonsignificant associations were found between time of BMI measurement during childhood and cancer‐site‐specific analyses. Conclusions We found little evidence of any associations between early life adiposity on later life CRC risk.
AbstractList Varying obesogenic inherited predisposition in early to later life may differentially impact colorectal cancer (CRC) development. Previous Mendelian randomization (MR) studies, conducted in populations of European genetic similarity, have not observed any significant associations between early life body weight with CRC risk. However, it remains unclear whether body mass index (BMI) at different early lifetime points is causally related with CRC risk in both Europeans and East Asian populations. We conducted a two-sample MR study to investigate potential causal relationships between genetically predicted BMI during early life (birth to 8 years old) and at specific periods (birth, transient, early rise and late rise) and CRC risk. Summary data were obtained from genome-wide association study (GWAS) of BMI in 28 681 children from the Norwegian Mother, Father and Child Cohort Study (MoBa) study and applied to CRC GWAS data from European and East Asian descent populations (102 893 cases and 485 083 non-cases). There were no significant associations observed between early life BMI and CRC risk in European or East Asian populations. The effect estimates were similar in European studies (odds ratio [OR] per a 1-standard deviation [SD] increase: 1.01, 95% confidence interval [CI]: 0.95, 1.07) and in East Asians (OR per a 1-SD increase: 1.02, 95% CI: 0.91, 1.14). Similar nonsignificant associations were found between time of BMI measurement during childhood and cancer-site-specific analyses. We found little evidence of any associations between early life adiposity on later life CRC risk.
Summary Background Varying obesogenic inherited predisposition in early to later life may differentially impact colorectal cancer (CRC) development. Previous Mendelian randomization (MR) studies, conducted in populations of European genetic similarity, have not observed any significant associations between early life body weight with CRC risk. However, it remains unclear whether body mass index (BMI) at different early lifetime points is causally related with CRC risk in both Europeans and East Asian populations. Objectives We conducted a two‐sample MR study to investigate potential causal relationships between genetically predicted BMI during early life (birth to 8 years old) and at specific periods (birth, transient, early rise and late rise) and CRC risk. Methods Summary data were obtained from genome‐wide association study (GWAS) of BMI in 28 681 children from the Norwegian Mother, Father and Child Cohort Study (MoBa) study and applied to CRC GWAS data from European and East Asian descent populations (102 893 cases and 485 083 non‐cases). Results There were no significant associations observed between early life BMI and CRC risk in European or East Asian populations. The effect estimates were similar in European studies (odds ratio [OR] per a 1‐standard deviation [SD] increase: 1.01, 95% confidence interval [CI]: 0.95, 1.07) and in East Asians (OR per a 1‐SD increase: 1.02, 95% CI: 0.91, 1.14). Similar nonsignificant associations were found between time of BMI measurement during childhood and cancer‐site‐specific analyses. Conclusions We found little evidence of any associations between early life adiposity on later life CRC risk.
Author Hughes, David J.
Phipps, Amanda I.
Platz, Elizabeth A.
Murphy, Neil
Jenab, Mazda
Cheng, Iona
Pai, Rish K.
Kweon, Sun‐Seog
Le Marchand, Loic
Brenner, Hermann
Chen, Zhishan
Zheng, Wei
Moreno, Victor
Peters, Ulrike
Duijnhoven, Fränzel J. B.
Papadimitriou, Nikos
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Issue 1
Keywords colorectal cancer
mendelian randomization
obesity
early life
Language English
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2024 The Author(s). Pediatric Obesity published by John Wiley & Sons Ltd on behalf of World Obesity Federation.
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Notes Where authors are identified as personnel of the International Agency for Research on Cancer/World Health Organization, the authors alone are responsible for the views expressed in this article and they do not necessarily represent the decisions, policy or views of the International Agency for Research on Cancer/World Health Organization. This article is the result of the scientific work of Dr. Murphy while he was affiliated at IARC.
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Snippet Summary Background Varying obesogenic inherited predisposition in early to later life may differentially impact colorectal cancer (CRC) development. Previous...
Varying obesogenic inherited predisposition in early to later life may differentially impact colorectal cancer (CRC) development. Previous Mendelian...
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SubjectTerms Adult
Asia, Eastern - epidemiology
Body Mass Index
Child
Child, Preschool
colorectal cancer
Colorectal Neoplasms - epidemiology
Colorectal Neoplasms - genetics
early life
East Asian People - genetics
Female
Genetic Predisposition to Disease
Genome-Wide Association Study
Humans
Infant
Infant, Newborn
Male
mendelian randomization
Mendelian Randomization Analysis
Norway - epidemiology
obesity
Polymorphism, Single Nucleotide
Risk Factors
White People - genetics
Title Body mass index at birth and early life and colorectal cancer: A two‐sample Mendelian randomization analysis in European and East Asian genetic similarity populations
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https://www.ncbi.nlm.nih.gov/pubmed/39587448
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