4 research outputs found

    Burden of disease attributable to high body mass index: an analysis of data from the Global Burden of Disease Study 2021

    Get PDF
    Background Obesity represents a major global health challenge with important clinical implications. Despite its recognized importance, the global disease burden attributable to high body mass index (BMI) remains less well understood. Methods We systematically analyzed global deaths and disability-adjusted life years (DALYs) attributable to high BMI using the methodology and analytical approaches of the Global Burden of Disease Study (GBD) 2021. High BMI was defined as a BMI over 25 kg/m2 for individuals aged ≥20 years. The Socio-Demographic Index (SDI) was used as a composite measure to assess the level of socio-economic development across different regions. Subgroup analyses considered age, sex, year, geographical location, and SDI. Findings From 1990 to 2021, the global deaths and DALYs attributable to high BMI increased more than 2.5-fold for females and males. However, the age-standardized death rates remained stable for females and increased by 15.0% for males. Similarly, the age-standardized DALY rates increased by 21.7% for females and 31.2% for males. In 2021, the six leading causes of high BMI-attributable DALYs were diabetes mellitus, ischemic heart disease, hypertensive heart disease, chronic kidney disease, low back pain and stroke. From 1990 to 2021, low-middle SDI countries exhibited the highest annual percentage changes in age-standardized DALY rates, whereas high SDI countries showed the lowest. Interpretation The worldwide health burden attributable to high BMI has grown significantly between 1990 and 2021. The increasing global rates of high BMI and the associated disease burden highlight the urgent need for regular surveillance and monitoring of BMI

    Limitations of the DiaRem Score in Predicting Remission of Diabetes Following Roux-En-Y Gastric Bypass (RYGB) in an ethnically Diverse Population from a Single Institution in the UK

    Get PDF
    Purpose This study aimed to determine the predictive power of the DiaRem score following Roux-en-Y gastric bypass to identify patients who would have diabetes remission at 1 year in an ethnically diverse population. Methods We performed a retrospective review of 262 patients with type 2 diabetes mellitus who underwent RYGB at the Imperial Weight Centre, UK, from 2007 to 2014. Data was collected on the parameters required to calculate the DiaRem score as well as pre- and post-surgical weight and the ethnicity of the subjects. Results The studied cohort was ethnically diverse (61.3 % Caucasian, 10.3 % Asian, 5.3 % black, 2.6 % mixed and 20.6 % other). At 1-year post-surgery, there were significant reductions in mean weight (133.4 to 94.3 kg) and BMI (46.7 to 33.3 kg/m2). The mean HbA1c decreased from 8.2 to 6.1 %, and 32.5 % of the cohort underwent either partial or complete remission. 67.8 % of the patients that were classified in group 1 of the DiaRem score (most likely to have remission) had complete remission. However, 22.9 % of the patients predicted to have the least chance of remission had either partial or complete remission. Conclusions In this ethnically diverse cohort, the DiaRem score remains a useful tool to predict diabetes remission in those that have a low DiaRem score (high chance for remission) but was more limited in its predictive power in those with a high DiaRem score (least likely to have remission). Caution must be used in the application of this model in populations other than the US white Caucasian population used to derive the score

    Global burden of metabolic diseases, 1990-2021

    Get PDF
    BACKGROUND: Common metabolic diseases, such as type 2 diabetes mellitus (T2DM), hypertension, obesity, hypercholesterolemia, and metabolic dysfunction-associated steatotic liver disease (MASLD), have become a global health burden in the last three decades. The Global Burden of Disease, Injuries, and Risk Factors Study (GBD) data enables the first insights into the trends and burdens of these metabolic diseases from 1990 to 2021, highlighting regional, temporal and differences by sex.METHODS: Global estimates of disability-adjusted life years (DALYs) and deaths from GBD 2021 were analyzed for common metabolic diseases (T2DM, hypertension, obesity, hypercholesterolemia, and MASLD). Age-standardized DALYs (mortality) per 100,000 population and annual percentage change (APC) between 1990 and 2021 were estimated for trend analyses. Estimates are reported with uncertainty intervals (UI).RESULTS: In 2021, among five common metabolic diseases, hypertension had the greatest burden (226 million [95 % UI: 190-259] DALYs), whilst T2DM (75 million [95 % UI: 63-90] DALYs) conferred much greater disability than MASLD (3.67 million [95 % UI: 2.90-4.61]). The highest absolute burden continues to be found in the most populous countries of the world, particularly India, China, and the United States, whilst the highest relative burden was mostly concentrated in Oceania Island states. The burden of these metabolic diseases has continued to increase over the past three decades but has varied in the rate of increase (1.6-fold to 3-fold increase). The burden of T2DM (0.42 % [95 % UI: 0.34-0.51]) and obesity (0.26 % [95 % UI: 0.17-0.34]) has increased at an accelerated rate, while the rate of increase for the burden of hypertension (-0.30 % [95 % UI: -0.34 to -0.25]) and hypercholesterolemia (-0.33 % [95 % UI: -0.37 to -0.30]) is slowing. There is no significant change in MASLD over time (0.05 % [95 % UI: -0.06 to 0.17]).CONCLUSION: In the 21st century, common metabolic diseases are presenting a significant global health challenge. There is a concerning surge in DALYs and mortality associated with these conditions, underscoring the necessity for a coordinated global health initiative to stem the tide of these debilitating diseases and improve population health outcomes worldwide.</p

    Clinical and genomic factors influencing type 2 diabetes remission after bariatric surgery

    Full text link
    Bariatric surgery is currently the most effective treatment for type 2 diabetes (T2DM), in some cases inducing complete remission within days of surgery. The mechanisms driving this phenomenon remain unclear. This thesis describes the collection of clinical and genomic information from participants of the Personalised Medicine for Morbid Obesity (PMMO) study undergoing Roux-en-Y gastric bypass or vertical gastrectomy, investigates the ability of clinical and genomic factors to predict diabetes remission following surgery, and identifies early post-surgery changes in gene expression that may drive remission. Although most T2DM improves to some extent following bariatric surgery, not everyone achieves remission. Scoring systems to predict remission help to ensure that limited NHS resources are directed towards those most likely to benefit: an early aim was to explore how these might be improved. Two such scores, DiaRem and Advanced-DiaRem, were applied to the PMMO cohort, along with the individual clinical factors of T2DM duration and number of prescribed T2DM drugs. Advanced-DiaRem had greatest predictive value in this heterogeneous cohort, particularly in non-insulin-treated participants for whom remission prediction scores have generally decreased efficacy. Identification of genomic predictors of diabetes remission may reveal more about the aetiology of diabetes and why people respond differently to bariatric surgery. Using RNA-sequencing and quantitative polymerase chain reaction (qPCR) a transcript of HMGCS1 (required for de novo cholesterol biosynthesis) was identified as a genomic predictor of T2DM remission after Roux-en-Y gastric bypass. This is the first transcriptomics biomarker identified as predictive of T2DM remission from pre-surgery peripheral blood. I also describe the first study comparing early post-operative transcriptomic profiles between remission and non-remission groups. Transcripts of ANXA6 (which regulates intracellular cholesterol distribution, further implicating bile-acids in the mechanisms of remission) and TRAF1 (which regulates NF-kB pathways) were differentially expressed in RNA-sequencing data, but this was not confirmed by qPCR analyses.Open Acces
    corecore