Macronutrients and Metabolic Health - Understanding how metabolic disease arises at the population level using metabolomics and lipidomics.
Macronutrients and Metabolic Health - Understanding how metabolic disease arises at the population level using metabolomics and lipidomics.
批准号:
MR/P011705/2
负责人:
Julian Griffin
金额:
$62.06万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2020
资助国家:
英国
项目状态:
已结题
起止时间:
2020 至 --
中文摘要
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英文摘要
Both obesity and type 2 diabetes (T2DM) are increasing in the UK, placing significant pressure on the National Health Service and impacting on the health of the UK. We know that some of the major causes of these increases are associated with increased dietary consumption of fats and sugars, as well as a general decrease in physical activity. While current public health advice is to exercise more and eat less calorie dense foods, this health advice has been unable to halt the increases in either obesity or T2DM. While there are a number of drugs used to treat T2DM and the increased fat concentrations found in the blood of individuals with obesity, many have side effects which complicate their long term use and are costly to administer. One central question to the field of diabetes research is why on an individual basis certain people are predisposed to developing insulin resistance (a pre-diabetic state) and subsequent T2DM while others stay metabolically healthy. Addressing this question could help treat those at risk of progression and have a significant impact on the costs of treating this disease and its complications.In order to do this we use analytical chemistry techniques, including mass spectrometry and Nuclear Magnetic Resonance (NMR) spectroscopy, to measure the total small molecule complement of tissues, cells and biofluids to develop a fingerprint of those metabolites that are associated with disease using a combination of multivariate statistics and pattern recognition techniques. This approach is termed metabolomics. By modelling changes in these metabolites as disease progresses we build up an 'atlas' of response in terms of the key metabolic perturbations associated with the disease. In particular this approach allows us to look at how food intake influences the metabolism of the body, and we can model these changes to look at diet-genotype interactions induced by over-nutrition (eating too much food).To achieve this aim we have identified four themes to be developed in parallel.1. Fat cells in health and disease: It is well established that fat cells (referred to as white adipose tissue) have numerous important roles in maintaining healthy metabolism in addition to their role as a major site for storage of fats, including roles in regulating hormones, maintaining body temperature and even contributing to the body clock. We will apply metabolomics in conjunction with molecular biology tools to investigate the balance between lipid storage and how we might influence fat metabolism to reduce obesity. 2. Ectopic fat deposition: Once the capability of white adipose tissue to store fat has been exceeded, fat deposition occurs inappropriately (ectopically) in other tissues. While the consequences of raised blood glucose are biochemically well defined, we do not understand what the consequences of raised fat concentrations are. We will use comprehensive metabolomic approaches to profile the impact of excessive fat storage in the liver, heart and skeletal muscle, and in particular focus on the progression of fatty liver disease. 3. Lipidomics at the epidemiology scale: While most animal models are caused by rare errors in single genes which cause T2DM, the most common forms found in patients with diabetes are caused by many genes with a strong environmental interaction, particularly as the result of over nutrition and increased sedentary lifestyles. In order to investigate IR and T2DM development in humans we have developed assays that can be performed on a global scale to allow us to address questions about T2DM and diet, ethnicity and age in epidemiology studies.4. Method development in mass spectrometry and bioinformatics: To be able to conduct these studies we require being at the forefront of developments in both mass spectrometry and mathematical tools for processing the data. We are currently developing tools in mass spectrometry imagining and ion mobility for lipidomics.
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DOI:
10.1038/s41598-022-05562-8
发表时间:
2022-01-26
期刊:
Scientific reports
影响因子:
4.6
作者:
[Adebayo AS, Roman M, Zakkar M, Yusoff S, Gulston M, Joel-David L, Anthony B, Lai FY, Murgia A, Eagle-Hemming B, Sheikh S, Kumar T, Aujla H, Dott W, Griffin JL, Murphy GJ, Woźniak MJ]
通讯作者:
Woźniak MJ
DOI:
10.1371/journal.pone.0251233
发表时间:
2021
期刊:
PloS one
影响因子:
3.7
作者:
[Haim-Vilmovsky L, Henriksson J, Walker JA, Miao Z, Natan E, Kar G, Clare S, Barlow JL, Charidemou E, Mamanova L, Chen X, Proserpio V, Pramanik J, Woodhouse S, Protasio AV, Efremova M, Griffin JL, Berriman M, Dougan G, Fisher J, Marioni JC, McKenzie ANJ, Teichmann SA]
通讯作者:
Teichmann SA
DOI:
10.1016/j.cell.2021.12.046
发表时间:
2022-02-03
期刊:
Cell
影响因子:
64.5
作者:
[Dejnirattisai W, Huo J, Zhou D, Zahradník J, Supasa P, Liu C, Duyvesteyn HME, Ginn HM, Mentzer AJ, Tuekprakhon A, Nutalai R, Wang B, Dijokaite A, Khan S, Avinoam O, Bahar M, Skelly D, Adele S, Johnson SA, Amini A, Ritter TG, Mason C, Dold C, Pan D, Assadi S, Bellass A, Omo-Dare N, Koeckerling D, Flaxman A, Jenkin D, Aley PK, Voysey M, Costa Clemens SA, Naveca FG, Nascimento V, Nascimento F, Fernandes da Costa C, Resende PC, Pauvolid-Correa A, Siqueira MM, Baillie V, Serafin N, Kwatra G, Da Silva K, Madhi SA, Nunes MC, Malik T, Openshaw PJM, Baillie JK, Semple MG, Townsend AR, Huang KA, Tan TK, Carroll MW, Klenerman P, Barnes E, Dunachie SJ, Constantinides B, Webster H, Crook D, Pollard AJ, Lambe T, OPTIC Consortium, ISARIC4C Consortium, Paterson NG, Williams MA, Hall DR, Fry EE, Mongkolsapaya J, Ren J, Schreiber G, Stuart DI, Screaton GR]
通讯作者:
Screaton GR
DOI:
10.3390/nu13082768
发表时间:
2021-08-12
期刊:
Nutrients
影响因子:
5.9
作者:
[Belcastro L, Ferreira CS, Saraiva MA, Mucci DB, Murgia A, Lai C, Vigor C, Oger C, Galano JM, Pinto GDA, Griffin JL, Torres AG, Durand T, Burton GJ, Sardinha FLC, El-Bacha T]
通讯作者:
El-Bacha T
Histone acetyltransferase NAA40 modulates acetyl-CoA levels and lipid synthesis.
组蛋白乙酰转移酶NAA40调节乙酰-COA水平和脂质合成。
DOI:
10.1186/s12915-021-01225-8
发表时间:
2022-01-20
期刊:
BMC biology
影响因子:
5.4
作者:
[Charidemou E, Tsiarli MA, Theophanous A, Yilmaz V, Pitsouli C, Strati K, Griffin JL, Kirmizis A]
通讯作者:
Kirmizis A
High resolution mass spectrometry across the metabolome and lipidome: from single cells to cohorts
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批准号:MR/X012700/1
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项目类别:Research Grant
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资助金额:$63.3万
-
财政年份:2022
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负责人:Julian Griffin
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依托单位:
Identification of specific metabolites in mycolactone producing mycobacteria and Buruli ulcer infection: diagnostic biomarkers through metabolomic
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批准号:MR/P024416/1
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项目类别:Research Grant
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资助金额:$28.45万
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财政年份:2017
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负责人:Julian Griffin
-
依托单位:
Macronutrients and Metabolic Health - Understanding how metabolic disease arises at the population level using metabolomics and lipidomics.
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批准号:MR/P011705/1
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项目类别:Research Grant
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资助金额:$266.28万
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财政年份:2016
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负责人:Julian Griffin
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依托单位:
The Cambridge Initiative: Proposal to enhance linked research in human fat metabolism and pathophysiology between MRC HNR, MRC MDU and MRC Epi
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批准号:MR/P01836X/1
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项目类别:Research Grant
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资助金额:$74.0万
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财政年份:2016
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负责人:Julian Griffin
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依托单位:
Burning fat: an in vivo and in vitro study of the role of PPAR-delta in regulating fat metabolism in adipose tissue
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批准号:BB/H013539/2
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项目类别:Research Grant
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资助金额:$46.37万
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财政年份:2012
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负责人:Julian Griffin
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依托单位:
Burning fat: an in vivo and in vitro study of the role of PPAR-delta in regulating fat metabolism in adipose tissue
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批准号:BB/H013539/1
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项目类别:Research Grant
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资助金额:$64.3万
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财政年份:2010
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负责人:Julian Griffin
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依托单位:
Ion-trap mass spectrometry for integrative biology
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批准号:BB/D524824/1
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项目类别:Research Grant
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资助金额:$16.98万
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财政年份:2006
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负责人:Julian Griffin
-
依托单位:
The application of time domain processes for the improvement of data quality and enhanced pattern recognition in NMR based metabolomics
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批准号:BB/D01638X/1
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项目类别:Research Grant
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资助金额:$31.33万
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财政年份:2006
-
负责人:Julian Griffin
-
依托单位:
国内基金
海外基金
丝氨酸/甘氨酸/一碳代谢网络(SGOC metabolic network)调控炎症性巨噬细胞活化及脓毒症病理发生的机制研究
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批准号:81930042
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项目类别:重点项目
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资助金额:305.0万元
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批准年份:2019
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负责人:王迪
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依托单位: