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      Long-term cost-effectiveness of interventions for obesity: A mendelian randomisation study

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          Abstract

          Background

          The prevalence of obesity has increased in the United Kingdom, and reliably measuring the impact on quality of life and the total healthcare cost from obesity is key to informing the cost-effectiveness of interventions that target obesity, and determining healthcare funding. Current methods for estimating cost-effectiveness of interventions for obesity may be subject to confounding and reverse causation. The aim of this study is to apply a new approach using mendelian randomisation for estimating the cost-effectiveness of interventions that target body mass index (BMI), which may be less affected by confounding and reverse causation than previous approaches.

          Methods and findings

          We estimated health-related quality-adjusted life years (QALYs) and both primary and secondary healthcare costs for 310,913 men and women of white British ancestry aged between 39 and 72 years in UK Biobank between recruitment (2006 to 2010) and 31 March 2017. We then estimated the causal effect of differences in BMI on QALYs and total healthcare costs using mendelian randomisation. For this, we used instrumental variable regression with a polygenic risk score (PRS) for BMI, derived using a genome-wide association study (GWAS) of BMI, with age, sex, recruitment centre, and 40 genetic principal components as covariables to estimate the effect of a unit increase in BMI on QALYs and total healthcare costs. Finally, we used simulations to estimate the likely effect on BMI of policy relevant interventions for BMI, then used the mendelian randomisation estimates to estimate the cost-effectiveness of these interventions.

          A unit increase in BMI decreased QALYs by 0.65% of a QALY (95% confidence interval [CI]: 0.49% to 0.81%) per year and increased annual total healthcare costs by £42.23 (95% CI: £32.95 to £51.51) per person. When considering only health conditions usually considered in previous cost-effectiveness modelling studies (cancer, cardiovascular disease, cerebrovascular disease, and type 2 diabetes), we estimated that a unit increase in BMI decreased QALYs by only 0.16% of a QALY (95% CI: 0.10% to 0.22%) per year.

          We estimated that both laparoscopic bariatric surgery among individuals with BMI greater than 35 kg/m 2, and restricting volume promotions for high fat, salt, and sugar products, would increase QALYs and decrease total healthcare costs, with net monetary benefits (at £20,000 per QALY) of £13,936 (95% CI: £8,112 to £20,658) per person over 20 years, and £546 million (95% CI: £435 million to £671 million) in total per year, respectively.

          The main limitations of this approach are that mendelian randomisation relies on assumptions that cannot be proven, including the absence of directional pleiotropy, and that genotypes are independent of confounders.

          Conclusions

          Mendelian randomisation can be used to estimate the impact of interventions on quality of life and healthcare costs. We observed that the effect of increasing BMI on health-related quality of life is much larger when accounting for 240 chronic health conditions, compared with only a limited selection. This means that previous cost-effectiveness studies have likely underestimated the effect of BMI on quality of life and, therefore, the potential cost-effectiveness of interventions to reduce BMI.

          Abstract

          Sean Harrison and colleagues use Mendelian randomization techniques to estimate the cost effectiveness of interventions targeting body mass index.

          Author summary

          Why was this study done?
          • The prevalence of obesity has increased in the United Kingdom, and reliably measuring the impact on quality of life and the total healthcare cost from obesity is key to informing the cost-effectiveness of interventions that target obesity, and determining how much additional healthcare funding may be required should the trend of increasing obesity continue.

          • Current methods of examining cost-effectiveness of interventions for obesity may be subject to confounding and reverse causation, and previous studies also typically only use a limited number of health conditions to estimate the effects of BMI on quality of life, potentially underestimating the effects of BMI.

          • The aim of this study is to elucidate a new approach using mendelian randomisation for estimating the cost-effectiveness of interventions that target body mass index (BMI), which may be less affected by confounding and reverse causation than previous approaches.

          What did the researchers do and find?
          • Using mendelian randomisation, we estimated that a unit increase in BMI decreased quality-adjusted life years (QALYs) by 0.65% of a QALY per year and increased annual total healthcare costs by £42.23 per person.

          • Using these results and simulations, we estimated that, compared to no intervention and over 20 years, people aged 40 to 69 years in England or Wales with a BMI over 35 kg/m 2 receiving laparoscopic bariatric surgery would have, on average, an increase of 0.92 QALYs and a decrease in total healthcare costs of £5,096 per person.

          • We also estimated that restricting volume promotions for high fat, salt and sugar products would, across the 21.7 million adults aged 40 to 69 years in England and Wales, increase QALYs by 20,551 per year and decrease total healthcare costs by £137 million per year, and that between 1993 and 2017 in England and Wales, the increase in BMI of people aged 40 to 69 years led to a decrease of 1.13% of a QALY per year and an increase in annual healthcare costs of £69 per person.

          What do these findings mean?
          • Mendelian randomisation can be used to estimate the impact of interventions on quality of life and healthcare costs and is likely less biased than existing observational methods.

          • Interventions for BMI are likely to be cost-effective, possibly more so than previously anticipated using simulation methods that restrict the effect of changes in BMI on health conditions to cancer, cardiovascular disease, cerebrovascular disease, and type 2 diabetes.

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          Most cited references52

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          UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age

          Cathie Sudlow and colleagues describe the UK Biobank, a large population-based prospective study, established to allow investigation of the genetic and non-genetic determinants of the diseases of middle and old age.
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            The UK Biobank resource with deep phenotyping and genomic data

            The UK Biobank project is a prospective cohort study with deep genetic and phenotypic data collected on approximately 500,000 individuals from across the United Kingdom, aged between 40 and 69 at recruitment. The open resource is unique in its size and scope. A rich variety of phenotypic and health-related information is available on each participant, including biological measurements, lifestyle indicators, biomarkers in blood and urine, and imaging of the body and brain. Follow-up information is provided by linking health and medical records. Genome-wide genotype data have been collected on all participants, providing many opportunities for the discovery of new genetic associations and the genetic bases of complex traits. Here we describe the centralized analysis of the genetic data, including genotype quality, properties of population structure and relatedness of the genetic data, and efficient phasing and genotype imputation that increases the number of testable variants to around 96 million. Classical allelic variation at 11 human leukocyte antigen genes was imputed, resulting in the recovery of signals with known associations between human leukocyte antigen alleles and many diseases.
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              Principal components analysis corrects for stratification in genome-wide association studies.

              Population stratification--allele frequency differences between cases and controls due to systematic ancestry differences-can cause spurious associations in disease studies. We describe a method that enables explicit detection and correction of population stratification on a genome-wide scale. Our method uses principal components analysis to explicitly model ancestry differences between cases and controls. The resulting correction is specific to a candidate marker's variation in frequency across ancestral populations, minimizing spurious associations while maximizing power to detect true associations. Our simple, efficient approach can easily be applied to disease studies with hundreds of thousands of markers.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: MethodologyRole: SoftwareRole: VisualizationRole: Writing – original draftRole: Writing – review & editing
                Role: ConceptualizationRole: MethodologyRole: SoftwareRole: Writing – review & editing
                Role: ConceptualizationRole: Funding acquisitionRole: MethodologyRole: SupervisionRole: Writing – review & editing
                Role: Funding acquisitionRole: Writing – review & editing
                Role: ConceptualizationRole: Funding acquisitionRole: MethodologyRole: Writing – review & editing
                Role: ConceptualizationRole: Funding acquisitionRole: MethodologyRole: SupervisionRole: Writing – review & editing
                Role: Academic Editor
                Journal
                PLoS Med
                PLoS Med
                plos
                PLoS Medicine
                Public Library of Science (San Francisco, CA USA )
                1549-1277
                1549-1676
                27 August 2021
                August 2021
                : 18
                : 8
                : e1003725
                Affiliations
                [1 ] MRC Integrative Epidemiology Unit (IEU), Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom
                [2 ] Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom
                [3 ] Research and Evaluation Division, Public Health Wales NHS Trust, Cardiff, United Kingdom
                [4 ] K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway
                Griffith University - Gold Coast Campus, AUSTRALIA
                Author notes

                The authors declare they have no conflicts of interest.

                Author information
                https://orcid.org/0000-0002-7966-0700
                https://orcid.org/0000-0001-5285-409X
                https://orcid.org/0000-0002-4265-2854
                https://orcid.org/0000-0003-3357-2796
                https://orcid.org/0000-0002-2460-0508
                Article
                PMEDICINE-D-20-02167
                10.1371/journal.pmed.1003725
                8437285
                34449774
                d910420f-ce64-41fe-8c41-65ceaa4a30e9
                © 2021 Harrison et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 18 May 2020
                : 9 July 2021
                Page count
                Figures: 5, Tables: 3, Pages: 24
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/501100000265, Medical Research Council;
                Award ID: MC_UU_00011/1
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100000269, Economic and Social Research Council;
                Award ID: ES/N000757/1
                Award Recipient :
                Funded by: Norwegian Research Council
                Award ID: 295989
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100000265, Medical Research Council;
                Award ID: MR/M020894/1
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100000265, Medical Research Council;
                Award ID: MR/P014259/1
                Award Recipient :
                Funded by: funder-id http://dx.doi.org/10.13039/501100000724, health foundation;
                Award ID: 807293
                Award Recipient :
                The Medical Research Council (MRC) and the University of Bristol support the MRC Integrative Epidemiology Unit [MC_UU_00011/1]. NMD is supported by an Economics and Social Research Council (ESRC) Future Research Leaders grant [ES/N000757/1] and the Norwegian Research Council Grant number 295989. LDH is supported by a Career Development Award from the UK Medical Research Council (MR/M020894/1). PD acknowledges support from a Medical Research Council Skills Development Fellowship (MR/P014259/1). This work is part of a project entitled ‘social and economic consequences of health: causal inference methods and longitudinal, intergenerational data’, which is part of the Health Foundation’s Social and Economic Value of Health Programme (Grant ID: 807293). The Health Foundation is an independent charity committed to bringing about better health and health care for people in the UK. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. This publication is the work of the authors, who serve as the guarantors for the contents of this paper.
                Categories
                Research Article
                Biology and Life Sciences
                Physiology
                Physiological Parameters
                Body Weight
                Body Mass Index
                Social Sciences
                Economics
                Economic Analysis
                Cost-Effectiveness Analysis
                Biology and Life Sciences
                Physiology
                Physiological Parameters
                Body Weight
                Obesity
                People and places
                Geographical locations
                Europe
                European Union
                United Kingdom
                England
                Medicine and Health Sciences
                Surgical and Invasive Medical Procedures
                Digestive System Procedures
                People and places
                Geographical locations
                Europe
                European Union
                United Kingdom
                Wales
                Medicine and Health Sciences
                Health Care
                Primary Care
                Medicine and Health Sciences
                Health Care
                Quality of Life
                Custom metadata
                vor-update-to-uncorrected-proof
                2021-09-13
                The empirical dataset is archived with UK Biobank and available to individuals who obtain the necessary permissions from the study’s data access committees, with data accessible from https://www.ukbiobank.ac.uk/. The code used to clean and analyse the data is available here: https://github.com/sean-harrison-bristol/Robust-causal-inference-for-long-term-policy-decisions.

                Medicine
                Medicine

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