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Observational Study
. 2016 Mar 8:352:i582.
doi: 10.1136/bmj.i582.

Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank

Affiliations
Observational Study

Height, body mass index, and socioeconomic status: mendelian randomisation study in UK Biobank

Jessica Tyrrell et al. BMJ. .

Abstract

Objective: To determine whether height and body mass index (BMI) have a causal role in five measures of socioeconomic status.

Design: Mendelian randomisation study to test for causal effects of differences in stature and BMI on five measures of socioeconomic status. Mendelian randomisation exploits the fact that genotypes are randomly assigned at conception and thus not confounded by non-genetic factors.

Setting: UK Biobank.

Participants: 119,669 men and women of British ancestry, aged between 37 and 73 years.

Main outcome measures: Age completed full time education, degree level education, job class, annual household income, and Townsend deprivation index.

Results: In the UK Biobank study, shorter stature and higher BMI were observationally associated with several measures of lower socioeconomic status. The associations between shorter stature and lower socioeconomic status tended to be stronger in men, and the associations between higher BMI and lower socioeconomic status tended to be stronger in women. For example, a 1 standard deviation (SD) higher BMI was associated with a £210 (€276; $300; 95% confidence interval £84 to £420; P=6 × 10(-3)) lower annual household income in men and a £1890 (£1680 to £2100; P=6 × 10(-15)) lower annual household income in women. Genetic analysis provided evidence that these associations were partly causal. A genetically determined 1 SD (6.3 cm) taller stature caused a 0.06 (0.02 to 0.09) year older age of completing full time education (P=0.01), a 1.12 (1.07 to 1.18) times higher odds of working in a skilled profession (P=6 × 10(-7)), and a £1130 (£680 to £1580) higher annual household income (P=4 × 10(-8)). Associations were stronger in men. A genetically determined 1 SD higher BMI (4.6 kg/m(2)) caused a £2940 (£1680 to £4200; P=1 × 10(-5)) lower annual household income and a 0.10 (0.04 to 0.16) SD (P=0.001) higher level of deprivation in women only.

Conclusions: These data support evidence that height and BMI play an important partial role in determining several aspects of a person's socioeconomic status, especially women's BMI for income and deprivation and men's height for education, income, and job class. These findings have important social and health implications, supporting evidence that overweight people, especially women, are at a disadvantage and that taller people, especially men, are at an advantage.

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Conflict of interest statement

Competing interests: All authors have completed the ICMJE uniform disclosure form at www.icmje.org/coi_disclosure.pdf and declare: no support from any organisation for the submitted work other than detailed above; MNW has received speakers fees from Ipsen and Merck, and TMF has consulted for Boehringer Ingelheim; no other relationships or activities that could appear to have influenced the submitted work.

Figures

None
Fig 1 Principle of mendelian randomisation: if height or body mass index (BMI) causally influences socioeconomic status, genetic variants associated with that trait will also be associated with socioeconomic status. As genotype is assigned at conception, it should not be associated with factors that normally confound the association between BMI and height and socioeconomic status (eg, environmental and behavioural factors). We can use our estimates of the genetic-height/BMI association (w) and the genetic-socioeconomic status association (x) to infer the causal effect of height or BMI on socioeconomic status (y=x/w), which is expected to be free from confounding. If the estimated causal effect (y) is different from the observational association between the height or BMI and socioeconomic status, this would suggest that the observational association is confounded (assuming that the assumptions of the mendelian randomisation analyses are valid). SNP=single nucleotide polymorphism

Comment in

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