The Other Pandemic: Obesity Anastasia Economou Introduction

Total Page:16

File Type:pdf, Size:1020Kb

The Other Pandemic: Obesity Anastasia Economou Introduction The other pandemic: Obesity Anastasia Economou Introduction Obesity is defined as “abnormal or excessive fat accumulation that presents a risk to health” (World Health Organisation, [WHO], 2020). The Body Mass Index (BMI), weight is divided by height squared, is used to screen for obesity: a person ≥30 kg/m2 is ‘obese’; between 25 kg/m2 and 30 kg/m2 is ‘overweight’. In 2016, 1.6 billion adults (18 years +), were overweight, of which 650 million were obese. Obesity is a major burden of disease (WHO, 2020) not only in high-income countries, but also in low-income (e.g. Eritrea) and middle income countries (e.g. India) (Malik, Willett & Hu, 2013). Obesity has become a pandemic with projections pointing to 38% of Earth’s population becoming overweight and 20% obese by 2030 (Anekwe et al., 2020). Obesity in the UK is also on the rise: it affects 1 in 4 adults, 1 in 10 children aged 4-5, and 1 in 5 children aged 10-11 (NHS, 2020). 63% of adults and 33% of children leaving primary school are above a healthy weight (Public Health England, [PHE], 2020). Obesity is linked to a number of chronic and debilitating conditions like cardio- metabolic risk (CMR) (i.e. metabolic syndrome, diabetes, hypertension, dyslipidaemia, cardiovascular disease or stroke) and to conditions such as depression which can impact on an individual’s lifecycle. This paper will explore these links and further look at food insecurity and how it could contribute to obesity as well as how socioeconomic inequalities impact on this. It will then seek to evaluate the latest policy of the UK government on ‘Tackling Obesity: empowering adults and children to live healthier lives’ (UK Government, 2020) with a view to exploring whether this policy is appropriate in addressing food insecurity to prevent obesity. It will then conclude with some recommendations. Discussion Obesity imposes risks on cardio-metabolic health i.e. on the chances of developing metabolic syndrome, diabetes, hypertension, dyslipidaemia, cardiovascular disease or stroke (Malik et al., 2009). Four different phenotypes in obesity have been identified: a) Metabolically Healthy Obese (MHO) – have: Low Visceral Fat, High Fat Mass, High Insulin Resistance, High HDL and Low Triglycerides b) Metabolically Healthy – have: Low Visceral Fat, Low BMI, Low Fat Mass, High Lean Body Mass, High Insulin Sensitivity, Low Liver Fat, Low Triglycerides. c) Metabolically Obese Normal Weight (MONW) – have: High Visceral Fat, Low BMI, High Fat Mass, Low Lean Body Mass, Low Insulin Sensitivity, High Liver Fat, High Triglycerides. d) “At risk” obese – have: High Visceral Fat, High BMI, High Fat Mass, Low Insulin Sensitivity, Low HDL, High Triglycerides (Karelis, Brochu, Rabasa‐Lhoret, Garrel, & Poehlman, 2004). In order to identify when an individual runs a CMR, the use of BMI alone is not sufficient because it does not provide information about the fat distribution and concentration. Subcutaneous abdominal adipose tissue (SAAT) and internal (visceral and ectopic deposits i.e. into organs such as liver and pancreas, and around muscles) adipose tissue have been found to have very serious consequences for cardio metabolic health (Piche, Poirier, Lemieux & DesprѐMs, 2018, Thomas, Frost, Taylor-Robinson & Bell, 2012). Some studies have found that increased adiposity, without an increase in liver fat, does not cause metabolic syndrome (Magkos, 2019). Tomiyama, Hunger, Nguyen-Cuu and Wells (2016) found that half of overweight individuals, and 45% of obese individuals, were cardio-metabolically healthy while 30% of the study population who had ‘normal’ BMI were found to be cardio- metabolically unhealthy. 35% of all people with obesity in the world are metabolically healthy (Lin, Zhang Zheng & Zheng, 2017); they have half the risk of developing T2DM and CVD compared with metabolically unhealthy people with obesity but 50-300% increased risk when compared with metabolically healthy normal weight people. 50% of metabolically healthy obese people will become metabolically unhealthy within 10 yrs if they do not make lifestyle changes (Magkos, 2019). MONW is associated with significant cardiometabolic dysregulation (Karelis et al., 2004), including metabolic syndrome and CVD risk factors and increased CVD mortality in women (Romero-Corral et al., 2010). The MONW phenotype has been further investigated using Magnetic Resonance Imaging (MRI) and showed that many thin people carry more visceral adipose tissue (VAT) than overweight or obese people leading to the identification of the TOFI (thin-on-the-outside fat- on-the-inside) sub-phenotype which has been observed to also increase CMR (Thomas et al., 2012). Qualitative aspects of diet, type of foods and dietary patterns, may affect the development and distribution of VAT as well as the SAAT; with VAT being particularly impacted by the quality of diet and physical inactivity (Fischer, Pick, Moewes & Nöthlings, 2015) as well as ageing, sex hormones, dietary composition and genetic factors (Thomas et al., 2012). Depression has also been linked to obesity. Depression is “a common mental disorder that causes people to experience depressed mood, loss of interest or pleasure, feelings of guilt or low self-esteem, disturbed sleep or appetite, low energy and poor concentration” (MHF, 2016). Depression is the predominant mental health disorder – 3.4% world wide (out of 10.7% people with mental health disorder). In the UK, it affects 3% of males and 3.8% of females (MHF, 2016). In 2013, depression was the second leading cause for years lived with disability (WHO, 2018). Mental unwellness is the second-largest source of burden of disease in England (Mental Health First Aid England, 2020). Obesity can raise twice the risk of becoming depressed (Roberts, Deleger, Strawbridge & Kaplan, 2003) especially for women (Tyrrell et al., 2019; Pereira- Miranda, Costa, Queiroz, Pereira-Santos & Santana , 2016; Jung et al., 2017; Roberts et al., 2003), those of older age and those who have financial difficulties (Jung et al., 2017; Roberts et al., 2003). Obesity may lead to negative self- perception, restrictive diets and a vicious circle of weight loss and gain, binge eating and depression. Obese people can feel guilty and ashamed and may isolate themselves which enhances the risk of depression (Pereira-Miranda et al. 2016). They may experience stigmatisation in the community, by health professionals and in job settings which can exacerbate the negative feelings they already experience and lead to depression (Puhl, Himmelstein & Pearl, 2020; Puhl & Heuer, 2009). Eating foods high in saturated fat and glycaemic index may affect the function of the brain (Ouakinin, Barreira & Gois, 2018; Pereira-Miranda et al., 2016). It seems that women with obesity and depression experience more devaluation compared to women with only one condition. Individuals with a higher level of internalized stigma, ingrained in the public stigma, may face great health obstacles (Luck-Sikorski, Schomerus, Steffi & Riedel-Heller, 2016). Depression also has been found to increase the risk of obesity. Blaine (2008) report 1.8 times increase in the risk while De Wit et al. (2010) found an 18% increase and that the risk is more pronounced in women. Adolescent girls have 2.5 times increase in the risk of becoming obese adults. (Blaine, 2008; Hasler et al., 2005). Low mood and low energy can lead to less activity and thus, excess energy intake which leads in itself to obesity. Lack of energy and inability to concentrate on tasks (like cooking) may also lead to the consumption of low quality diet. Depression may lead to comfort food (Di Renzo et al., 2020; Jeffery et al., 2009) which is often high in refined sugars, saturated fat and calories and can lead to weight gain. There also has been found a reciprocal association between obesity and depression. The findings regarding the risk vary. Luppino et al., (2010) found the risk for people with obesity to develop depression was 55% while the risk for people with depression to develop obesity was 58%. Mannan, Mamun, Doi and Clavarino (2016) found that depressed people had a 37% increased risk of being obese while 18% of obese people had an increased risk of being depressed and that in 10 year follow-up, the bi-directional relationship was even stronger for both men and women perhaps due to lifestyle and environmental influences. The bi-directional association is more likely in women (Rajan & Menon, 2017). Pan et al. (2012) found this in middle-aged and older women while Mannan et al., (2016) observed it in women aged 18-49. Women seem to be more vulnerable across their lifecycle than men to depression and obesity possibly due to biological, sociocultural, psychosocial and environmental influences (Morssinkhofa et al., 2020; Mannan et al., 2016). Stress can lead to depression (Le Moult, 2020) but stress is also linked to obesity (Tomiyama, 2019). It may be that there is a link between social and biological factors. The length of time may impact as well as strengthen the association between depression and obesity (Luppino et al., 2010). Mediouni, Madiouni and Kaczor-Urbanowicz (2020) propose the term ‘‘depreobesity’’ pointing to a modern epidemic characterised by the co- occurrence of depression and obesity. The relationship between obesity and depression is very complex and yet to be fully unravelled. There are social determinants of health and thus obesity (Marmot & Bell, 2019). These are the circumstances in which people are born, grow, live, work and age, and they “are influenced by the distribution of money, power and resources operating at global, national and local levels” WHO (2014, p.1). Food insecurity (FI) is a social determinant. The Food and Agriculture Organisation of the UN (2020) states that “A person is food insecure when they lack regular access to enough safe and nutritious food for normal growth and development and an active and healthy life. This may be due to unavailability of food and/or lack of resources to obtain food.
Recommended publications
  • Abdominal Obesity and Cardiovascular Disease
    Advances in Obesity Weight Management & Control Mini Review Open Access Abdominal obesity and cardiovascular disease Abstract Volume 3 Issue 2 - 2015 There is no doubt that obesity has become a major disease in modern times and it Rayan Saleh is definitely associated with cancer, neurodegeneration and heart disease. Scientific Department of Food and Nutritional Sciences, University of studies have resulted in a growing consensus on the way abdominal obesity is Reading, UK associated with inflammation and cardiometabolic risk. Although the gender is a substantial factor of having abdominal fat, there are other protective factors including Correspondence: Rayan Saleh, Registered Dietitian, healthy eating and physical activity. Several techniques are used to assess obesity Department of Food and Nutritional sciences, University of and their utilization depends on their feasibility and economic cost. This research is Reading, White knights, Reading, RG6 6AH, Berkshire, UK, designed to address the important relationship between abdominal obesity and the risk Email [email protected] of developing cardiovascular disease. Received: August 19, 2015 | Published: September 15, 2015 Keywords: abdominal obesity, metabolic syndrome, cardiovascular disease, body shape, inflammation, insulin resistance Abbreviations: WHO, world health organization; T2D, type to hip ratio WHR), bioelectrical impedance analysis (BIA), Dual 2 diabetes; BMI, body mass index; WC, waist circumference; WHR, energy X-ray absorptiometry (DXA), Computed tomography (CT) waist
    [Show full text]
  • The Obesity Paradox: a Statistical Outcome Or a Real Effect of Clinical Relevance?
    Review J Hypertens Res (2019) 5(4):162–166 The obesity paradox: a statistical outcome or a real effect of clinical relevance? Ivona Mitu1, Cristina Daniela Dimitriu2, O. Mitu3*, Manuela Ciocoiu4 1“Grigore T. Popa” University of Medicine and Pharmacy, Iasi, Romania, 2Department of Morpho-Functional Sciences (II), “Grigore T. Popa” University of Medicine and Pharmacy, Iasi, Romania 3Department of Medical Specialties (I), “Grigore T. Popa” University of Medicine and Pharmacy, Iasi, Romania 4Department of Morpho-Functional Sciences (II), “Grigore T. Popa” University of Medicine and Pharmacy, Iasi, Romania Received: October 10, 2019, Accepted: November 21, 2019 Abstract Obesity is one of the most important risk factors for morbidity and mortality, especially when referring to car- diovascular diseases. Different obesity phenotypes are presented in the medical literature, each one describing a different cardiovascular risk profile. The most important phenotype that is directly linked to the obesity paradox (OP) is the metabolically healthy obese phenotype, characterizing individuals with a BMI ≥ 30 kg/m2 and no metabolic abnormalities. This phenotype strengthens the true existence of the OP. In the same time we need to consider all the possible influencers when concluding if the OP is real and worth taking into consideration by clinicians. Analyzing studies that mention the OP, we observed several limitations either of the study itself or of the BMI used to classify obese patients. These limitations are described in the present review and they are of great importance in understanding how the OP is defined and how it should be interpreted. Keywords: obesity paradox, cardiovascular, BMI, obesity phenotypes. Introduction that the obesity prevalence has doubled since 1980, reaching 5% in children and 12% in adults [1].
    [Show full text]
  • Obesity, Diabetes and Longevity in the Gulf: Is There a Gulf Metabolic Syndrome?
    Obesity, diabetes and longevity in the Gulf: is there a Gulf Metabolic Syndrome? Article Published Version Open Access Guy, G. W., Nunn, A. V.W., Thomas, L. E. and Bell, J. D. (2009) Obesity, diabetes and longevity in the Gulf: is there a Gulf Metabolic Syndrome? International Journal of Diabetes Mellitus, 1 (1). pp. 43-54. ISSN 1877-5934 doi: https://doi.org/10.1016/j.ijdm.2009.05.001 Available at http://centaur.reading.ac.uk/35380/ It is advisable to refer to the publisher’s version if you intend to cite from the work. See Guidance on citing . To link to this article DOI: http://dx.doi.org/10.1016/j.ijdm.2009.05.001 Publisher: Elsevier All outputs in CentAUR are protected by Intellectual Property Rights law, including copyright law. Copyright and IPR is retained by the creators or other copyright holders. Terms and conditions for use of this material are defined in the End User Agreement . www.reading.ac.uk/centaur CentAUR Central Archive at the University of Reading Reading’s research outputs online This article appeared in a journal published by Elsevier. The attached copy is furnished to the author for internal non-commercial research and education use, including for instruction at the authors institution and sharing with colleagues. Other uses, including reproduction and distribution, or selling or licensing copies, or posting to personal, institutional or third party websites are prohibited. In most cases authors are permitted to post their version of the article (e.g. in Word or Tex form) to their personal website or institutional repository.
    [Show full text]
  • Understanding and Diagnosing Hyperinsulinaemia Catherine Crofts
    Understanding and Diagnosing Hyperinsulinaemia Catherine Crofts A thesis submitted to AUT University in fulfilment of the requirements for the degree of Doctor of Philosophy 2015 Human Potential Centre Primary Supervisor: Grant Schofield Secondary Supervisor: Caryn Zinn Tertiary Supervisor: Mark Wheldon Abstract Traditionally, insulin resistance is thought to be the precursor to many metabolic diseases. It is now believed that compensatory hyperinsulinaemia, previously thought to be a symptom of insulin resistance, may independently associated with metabolic disease and have its own pathological implications. Further understanding of compensatory hyperinsulinaemia may offer new insights into the aetiology of metabolic disease. This thesis provides novel work in hyperinsulinaemia and is broadly divided into four parts. Part 1 comprises a collation of the literature to show the aetiology and pathologies of hyperinsulinaemia, and to critically review the current diagnostic methods. The aetiology of hyperinsulinaemia is not yet fully elucidated, but is likely to include excessive carbohydrate ingestion, excessive cortisol or uric acid production, and/or medications. Subsequent pathologies include: cardio-, cerebro-, and peripheral- vascular disorders; type 2 diabetes; inflammation; and certain cancers or dementias. This is the first review to comprehensively link hyperinsulinaemia to such a wide range of metabolic disorders. Except for fasting insulin levels being considered unreliable, there was no consensus regarding diagnostic criteria. This means that diagnostic criteria needs to be determined prior to further research. Part 2 examined the prevalence of hyperinsulinaemia in the Kraft database. This important database comprises a large sample of oral glucose tolerance tests with insulin assays collected over 20 years in Chicago, USA. From the 15 000 available tests, those involving men aged ≥ 20 years and women ≥ 45 years, with a BMI > 18kg/m2 were included (n = 7750).
    [Show full text]
  • Cardiovascular Adipobiology: a Novel
    UDK 616.13-004.6-02 / Ser J Exp Clin Res 2008; 9 (3): 81 – 88 CARDIOVASCULAR ADIPOBIOLOGY: A NOVEL HEART-ASSOCIATED ADIPOSE TISSUE IN CARDIOVASCULAR DISEASE ABSTRACT 81 This article provides a conceptual framework for the possible role of myocardium. The present review highlights the possibility for tunica (i) periadventitial adipose tissue, and (ii) epicardial adipose tissue in adiposa and epicardial adipose tissue to play an important role in the pathogenesis of cardiovascular disease. Traditional concepts of an “outside-in” signaling in the development of atherosclerosis and atherogenesis are focused on luminal surface, where “inside-out” in- cardiomyopathy. In effect, adipose-targeted pharmacology and non- flammatory events trigger the extravasation of immune cells and the invasive measures might provide novel clinical insights into cardio- accumulation of lipids, smooth muscle cells and matrix components vascular adipobiology. Data of adipose-derived adipokines, including leading to atherosclerotic plaque formation. However, increasing evi- neurotrophic factors and neuropeptides, are also presented, raising a dence supports a new concept of an “outside-in” responses, involving hypothesis of neuroendocrine potential of adipose tissue; it may also periadventitial adipose tissue, herein referred to as tunica adiposa, be instrumental in the pathogenesis of cardiovascular disease. and epicardial adipose tissue, these two adipose loci functioning as Key words: adipokines, atherosclerosis, epicarial adipose tissue, secretory tissues. Thus, a paracrine signals originated from these tis- neurotrophic factors, neuropeptides, periadventitial adipose tissue sues could be transmitted into both the coronary artery intima and the INTRODUCTION “Ask yourself for each of your thoughts: is it a new one?” Carl Gustav Jung (1875-1961) Contemporary human lifestyle related to feeding and ered as the common denominators of the development physical activity can lead to an increasing accumula- of cardiovascular disease (1-4).
    [Show full text]
  • Fructose-Induced Inflammation and Increased Cortisol
    Progress in Cardiovascular Diseases xxx (2017) xxx–xxx Contents lists available at ScienceDirect Progress in Cardiovascular Diseases journal homepage: www.onlinepcd.com Fructose-induced inflammation and increased cortisol: A new mechanism for how sugar induces visceral adiposity James J. DiNicolantonio a,⁎, Varshil Mehta b, Neema Onkaramurthy c, James H. O'Keefe a a Saint Luke's Mid America Heart Institute, United States b MGM Medical College, Navi Mumbai, India c Kempegowda Institute of Medical Sciences, Bangalore, India article info abstract Available online xxxx Traditionally, the leading hypothesis regarding the development of obesity involves caloric imbalance, whereby Keywords: the amount of calories consumed exceeds the amount of calories burned which causes obesity. Another hypoth- Fructose esis for why we get fat has surfaced in the last decade which is the idea that the overconsumption of added sugars Sugar and refined carbohydrates induce insulin resistance and high insulin levels causing obesity. While insulin is a fat- Inflammation storing hormone, this hypothesis does not explain visceral adiposity, or why certain people are found to have fat Cortisol stored in and around their organs. We propose a new mechanism for body fattening, particular visceral adiposity. Visceral adiposity fl Fat This hypothesis involves the overconsumption of fructose, which leads to in ammation in all cells that metabo- Obesity lize it rapidly. When fructose is metabolized in subcutaneous adipocytes, the subsequent inflammation leads to an increase in intracellular cortisol in order to help squelch the inflammation. Unfortunately, the increase in in- tracellular cortisol leads to an increased flux of fatty acids out of the subcutaneous adipocytes allowing more sub- strate for fat storage into visceral fat tissue.
    [Show full text]
  • Lean, but Not Healthy: the 'Metabolically Obese, Normal-Weight'
    REVIEW CURRENT OPINION Lean, but not healthy: the ‘metabolically obese, normal-weight’ phenotype Cherlyn Dinga, Zhiling Chana, and Faidon Magkosa,b Purpose of review Obesity is commonly associated with metabolic dysfunction but there are obese persons who are 05/27/2020 on BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AWnYQp/IlQrHD3XI41p+sDLxbvlJvgPKJYKCChu4AQ7aSiyxN6Txunm8aAM3UyKGgK1Q== by https://journals.lww.com/co-clinicalnutrition from Downloaded Downloaded metabolically healthy. On the opposite side of the coin, there are lean persons who carry multiple cardiometabolic risk factors, typically referred to as metabolically obese, normal-weight (MONW). This from has called into question our understanding of obesity and metabolic dysfunction, as an appearance of https://journals.lww.com/co-clinicalnutrition normal weight may mask significant comorbidities and delay health interventions. Recent findings High heterogeneity in MONW prevalence rates has been observed, with estimates ranging from as low as 5% to as high as 45%. Reasons for this include sample size effects, differences in MONW definition, social and demographic factors, as well as assumptions made in establishing normal weight. MONW study participants are often characterized by excess visceral adipose tissue and ectopic fat deposition, by adipose tissue inflammation, altered inflammatory and adipokine profiles, reduced skeletal muscle mass BhDMf5ePHKav1zEoum1tQfN4a+kJLhEZgbsIHo4XMi0hCywCX1AWnYQp/IlQrHD3XI41p+sDLxbvlJvgPKJYKCChu4AQ7aSiyxN6Txunm8aAM3UyKGgK1Q== and low cardiorespiratory
    [Show full text]
  • The Importance of Diet Quality. Analysis of MAGNETIC Cohort
    Osadnik et al. Nutrition Journal (2020) 19:19 https://doi.org/10.1186/s12937-020-00532-0 RESEARCH Open Access Metabolically healthy obese and metabolic syndrome of the lean: the importance of diet quality. Analysis of MAGNETIC cohort Kamila Osadnik1, Tadeusz Osadnik1,2* , Marta Lonnie3, Mateusz Lejawa1, Rafał Reguła4, Martyna Fronczek5, Marcin Gawlita5,6, Lidia Wądołowska3, Mariusz Gąsior4 and Natalia Pawlas1 Abstract Background: Obesity is considered as an indispensable component of metabolic health assessment and metabolic syndrome diagnosis. The associations between diet quality and metabolic health in lean, young adults have not been yet established whilst data addressing this issue in overweight and obese subjects is scarce. Our analysis aimed to establish the link between diet quality (measured with data-driven dietary patterns and diet quality scores) and metabolic syndrome (MS) in young adults, regardless of their adiposity status. Methods: A total of 797 participants aged 18–35 years old were included in the study. Participants were assigned into metabolic syndrome (MS) group if at least two abnormalities within the following parameters were present: blood pressure, triglycerides, total cholesterol, HDL cholesterol, blood glucose. Participants with one or none abnormalities were considered as metabolically healthy subjects (MH), Diet quality was assessed with two approaches: 1) a posteriori by drawing dietary patterns (DPs) with principal component analysis (PCA) and 2) a priori by establishing diet quality scores and the adherence to pro-Healthy-Diet-Index (pHDI) and non-Healthy-Diet- Index (nHDI). Logistic regression with backward selection based on Akaike information criterion was carried out, to identify factors independently associated with metabolic health.
    [Show full text]
  • Metabolomic Signatures for Visceral Adiposity and Dysglycaemia in Asian Chinese and Caucasian European Adults: the Cross‑Sectional TOFI Asia Study Zhanxuan E
    Wu et al. Nutr Metab (Lond) (2020) 17:95 https://doi.org/10.1186/s12986-020-00518-z RESEARCH Open Access Metabolomic signatures for visceral adiposity and dysglycaemia in Asian Chinese and Caucasian European adults: the cross-sectional TOFI_Asia study Zhanxuan E. Wu1,2,3, Karl Fraser1,3,4* , Marlena C. Kruger2,4, Ivana R. Sequeira3,5, Wilson Yip3,5, Louise W. Lu3,5, Lindsay D. Plank6, Rinki Murphy3,7, Garth J. S. Cooper7,8, Jean‑Charles Martin9 and Sally D. Poppitt3,4,5,7 Abstract Background: Asian Chinese are more susceptible to deposition of visceral adipose tissue (VAT) and type 2 diabetes (T2D) development than European Caucasians when matched for gender, age and body mass index (BMI). Our aims were: (i) characterise the ethnicity‑specifc metabolomic signature of visceral adiposity measured by dual energy X‑ray absorptiometry (DXA) and fasting plasma glucose (FPG), and (ii) identify individuals susceptible to worse metabolic health outcomes. Methods: Fasting plasma samples from normoglycaemic (n 274) and prediabetic (n 83) participants were analysed with liquid chromatography–mass spectrometry using= untargeted metabolomics.= Multiple linear regression adjusting for age, gender and BMI was performed to identify metabolites associated with FPG and VAT calculated as percentage of total body fat (%VATTBF) in each ethnic group. Metabolic risk groups in each ethnicity were stratifed based on the joint metabolomic signature for FPG and %VATTBF and clinically characterised using partial least squares‑ discriminant analysis (PLS‑DA) and t‑tests. Results: FPG was correlated with 40 and 110 metabolites in Caucasians and Chinese respectively, with diglyceride DG(38:5) (adjusted β 0.29, p 3.00E 05) in Caucasians and triglyceride TG(54:4) (adjusted β 0.28, p 2.02E 07) in = = − = = − Chinese being the most signifcantly correlated metabolite based on the p‑value.
    [Show full text]
  • Westminsterresearch Phenotyping Ethnic Differences in Body Fat
    WestminsterResearch http://www.westminster.ac.uk/westminsterresearch Phenotyping Ethnic Differences in Body Fat Depots Alenaini, W. This is an electronic version of a PhD thesis awarded by the University of Westminster. © Ms Wareed Alenaini, 2019. The WestminsterResearch online digital archive at the University of Westminster aims to make the research output of the University available to a wider audience. Copyright and Moral Rights remain with the authors and/or copyright owners. Phenotyping Ethnic Differences in Body Fat Depots Wareed H. Alenaini A thesis submitted in partial fulfilment of the requirements of the University of Westminster for the degree of Doctor of Philosophy January 2019 1 Declaration of Originality The thesis has not previously been presented in any form to the University for assessment. I declare that all the materials contained in this thesis are my own work and any specific contribution or assistance is fully explained and appropriately referenced. 2 ABSTRACT There are remarkable ethnic differences in the incidence of metabolic syndrome associated features; including insulin resistance, type 2 diabetes, hypertension and cardiovascular diseases. Studies have suggested that South Asians (SA) present an unfavourable body fat phenotype, which includes a pattern of elevated visceral adipose tissue (VAT), and liver fat content; depots strongly associated with the progression of metabolic dysregulation. However, there are a limited number of studies examining body fat composition by ethnicity. The purpose of this thesis was to comprehensively phenotype VAT, abdominal subcutaneous adipose tissue (ASAT) and liver fat content in Caucasian (Cau), SA and Black African (BA) individuals from a large number of distinct populations. Here, I include data from three adult cohorts: the UK Biobank (n=9533) of mixed ethnicities, the DIRECT cohort (n=1553) of Cau pre-diabetic individuals and The West London Observation (TWLO) cohort (n=747) of mixed ethnicities.
    [Show full text]
  • Study Protocol
    Protocol Summary: HVN_Prediabetic Asian and Caucasian_TOFI_metabolomics Version FINAL_v4 Date: 03-Aug-2017 Author: Prof. SD Poppitt Page 1 of 23 High Value Nutrition – Priority Program Peak Nutrition for Metabolic Health [PANaMAH] CHARACTERISING THE PRE-DIABETIC ASIAN AND CAUCASIAN PHENOTYPE: THE ‘TOFI’ PROFILE identifying biomarkers of diabetic susceptibility and resilience using a metabolomics platform Sally Poppitt1, Karl Fraser2, Rinki Murphy1, Justin O’Sullivan1, John Ingram3 University of Auckland1, AgResearch2 and Plant & Food Research Ltd3 New Zealand In collaboration with Professor Garth Cooper, CADET, University of Manchester, UK; A/Prof Lindsay Plank, Department of Surgery Body Composition Unit, University of Auckland Study protocol Protocol Summary: HVN_Prediabetic Asian and Caucasian_TOFI_metabolomics Version FINAL_v4 Date: 03-Aug-2017 Author: Prof. SD Poppitt Page 2 of 23 PRINCIPAL INVESTIGATORS PROF. SALLY POPPITT PHD Professor of Human Nutrition Director, Human Nutrition Unit (HNU) School of Biological Sciences & Institute for Innovation in Biotechnology University of Auckland [email protected] DR KARL FRASER PHD Senior Research Scientist AgResearch Grasslands, Palmerston North [email protected] ASSOCIATE INVESTIGATORS DR RINKI MURPHY MBCHB, PHD Consultant endocrinologist, diabetes specialist Senior Lecturer, Department of Medicine University of Auckland & Auckland City Hospital [email protected] DR JUSTIN O’SULLIVAN PHD Research Fellow Liggins Institute University of Auckland [email protected]
    [Show full text]
  • Global Obesity Epidemic?
    WEIGHT IS NOT EVERYTHING Global obesity epidemic? The condition of obesity is the result of complex interactions between genetic and environmental factors. The diagnosis is based on the body mass index (BMI) de됍ned as the weight of the individual divided by the square of the height (kg/m2 ). The World Health Organization (WHO) in 2016 estimated that 39% of adults in the world are overweight (1.9 billion people with BMI between 20 and 25 kg / m2) while 13% are obese (650 million people with BMI greater than 30 kg / m2 ) . GLOBESITY is the term used to describe this global obesity epidemic. Furthermore, if we consider that a pregnant woman, if in a situation of overweight or obesity, can de됍ne the metabolic programming and the behavior that the unborn child will have towards food, we can easily realize the dimensions of GLOBESITY in the years to come. In 2019, the WHO estimated that 38 million children under the age of 5 are obese. Beyond the body mass index (BMI) Using only the body mass index, we can divide Using only the body mass index, we can divide the population into three large groups *: people of normal weight (BMI between 18.5 and 24.9 kg / m2), people who are overweight (BMI between 25 and 29.9 kg / m2) ) and obesity (BMI equal to or greater than 30 kg / m2). However, this index of measurement of fat mass, coined 150 years ago, does not take into account the real state of health and does not accurately de됍ne the degree of risk factor for the individual.
    [Show full text]