Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/26022
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dc.contributor.authorHandley, D-
dc.contributor.authorRafey, M-
dc.contributor.authorAlmansoori, S-
dc.contributor.authorBrazil, J-
dc.contributor.authorMcCarthy, A-
dc.contributor.authorAmin, H-
dc.contributor.authorO’Donnell, M-
dc.contributor.authorBlakemore, A-
dc.contributor.authorFinucane, F-
dc.date.accessioned2023-02-28T14:22:15Z-
dc.date.available2023-02-28T14:22:15Z-
dc.date.issued2022-11-09-
dc.identifier.citationFinucane FM., et al. (2022). ‘Higher Waist Hip Ratio Genetic Risk Score Is Associated with Reduced Weight Loss in Patients with Severe Obesity Completing a Meal Replacement Programme’ in Journal of Personalized Medicine., Vol.12(11)., pp.1-13. https://doi.org/10.3390/jpm12111881.en_US
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/26022-
dc.description.abstractBackground: A better understanding of the influence of genetic factors on the response to lifestyle interventions in people with obesity may allow the development of more personalised, effective and efficient therapeutic strategies. We sought to determine the influence of six obesity-related genetic risk scores on the magnitude of weight lost by patients with severe obesity who completed a dietary intervention. Methods: In this single-centre prospective cohort study, participants with severe and complicated obesity who completed a 24-week, milk-based meal replacement programme were genotyped to detect the frequency of common risk alleles for obesity and type 2 diabetes-related traits. Genetic risk scores (GRS) for six of these traits were derived. Participants with a potentially deleterious monogenic gene variant were excluded from the analysis. Results: In 93 patients completing the programme who were not carrying a known obesity-related gene mutation, 35.5% had diabetes, 53.8% were female, mean age was 51.4 ± 11 years, mean body mass index was 51.5 ± 8.7 and mean total weight loss percent at 24 weeks was 16 ± 6.3%. The waist–hip ratio (WHR) GRS was inversely associated with percentage total weight loss at 24 weeks (adjusted β for one standard deviation increase in WHR GRS −11.6 [−23.0, −0.3], p = 0.045), and patients in the lowest tertile of WHR GRS lost more weight. Conclusions: Patients with severe and complicated obesity with a genetic predisposition to central fat accumulation had less weight loss in a 24-week milk-based meal replacement programme, but there was no evidence for influence from the five other obesity-related genetic risk scores on the response to dietary restriction.en_US
dc.description.sponsorshipDale Handley and Hasnat Amin are grateful for the financial support of the College of Health, Medicine and Life Sciences at Brunel University London, UK. Sumaya Almansoori was funded by the Ministry of Higher Education, United Arab Emirates. Francis Finucane was funded by a Clinical Research Career Development Award from the Saolta University Healthcare Group and by a CURAM project grant from Science Foundation Ireland (Grant number P2-06).en_US
dc.format.extent1881 - 1881-
dc.languageen-
dc.publisherMDPI AGen_US
dc.rightsCopyright: © 2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).-
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/-
dc.subjectBariatricen_US
dc.subjectbody mass indexen_US
dc.subjectgenetic risk scoreen_US
dc.subjectmeal replacementen_US
dc.subjectmilken_US
dc.subjectsevere obesityen_US
dc.subjectsingle nucleotide polymorphismen_US
dc.subjectwaist–hip ratioen_US
dc.titleHigher Waist Hip Ratio Genetic Risk Score Is Associated with Reduced Weight Loss in Patients with Severe Obesity Completing a Meal Replacement Programmeen_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.3390/jpm12111881-
dc.relation.isPartOfJournal of Personalized Medicine-
pubs.issue11-
pubs.publication-statusPublished online-
pubs.volume12-
dc.identifier.eissn2075-4426-
Appears in Collections:Dept of Life Sciences Research Papers

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