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Lifestyle diseases and cardiovascular risk factors are interrelated to deficiencies of major substrates in ATP synthesis

Recent studies on diabetes and metabolic syndrome indicate a common disturbance of inorganic phosphate (Pi) metabolism. Pi is an important substrate in the formation of adenosine triphosphate (ATP), and many lifestyle diseases and cardiovascular risk factors similarly show deficiencies in either 1 o...

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Detalles Bibliográficos
Autores principales: Ditzel, Jørn, Lervang, Hans-Henrik
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952451/
https://www.ncbi.nlm.nih.gov/pubmed/20957128
http://dx.doi.org/10.2147/VHRM.S13368
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author Ditzel, Jørn
Lervang, Hans-Henrik
author_facet Ditzel, Jørn
Lervang, Hans-Henrik
author_sort Ditzel, Jørn
collection PubMed
description Recent studies on diabetes and metabolic syndrome indicate a common disturbance of inorganic phosphate (Pi) metabolism. Pi is an important substrate in the formation of adenosine triphosphate (ATP), and many lifestyle diseases and cardiovascular risk factors similarly show deficiencies in either 1 or 2 major components of ATP synthesis. Age, male gender, hypertension, obesity, hypertriglyceridemia, metabolic syndrome, and diabetes mellitus are all associated with hypophosphatemia. In addition, tobacco smoking, hyperchylomicronemia, hypertension, and diabetes may involve defects in tissue oxygen delivery. Hypophosphatemia may lead to a critical decrease in intracellular Pi and to mitochondrial dysfunction, which might be counter-acted by the pharmacological use of fructose 1,6-diphosphate.
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spelling pubmed-29524512010-10-18 Lifestyle diseases and cardiovascular risk factors are interrelated to deficiencies of major substrates in ATP synthesis Ditzel, Jørn Lervang, Hans-Henrik Vasc Health Risk Manag Review Recent studies on diabetes and metabolic syndrome indicate a common disturbance of inorganic phosphate (Pi) metabolism. Pi is an important substrate in the formation of adenosine triphosphate (ATP), and many lifestyle diseases and cardiovascular risk factors similarly show deficiencies in either 1 or 2 major components of ATP synthesis. Age, male gender, hypertension, obesity, hypertriglyceridemia, metabolic syndrome, and diabetes mellitus are all associated with hypophosphatemia. In addition, tobacco smoking, hyperchylomicronemia, hypertension, and diabetes may involve defects in tissue oxygen delivery. Hypophosphatemia may lead to a critical decrease in intracellular Pi and to mitochondrial dysfunction, which might be counter-acted by the pharmacological use of fructose 1,6-diphosphate. Dove Medical Press 2010-10-05 2010 /pmc/articles/PMC2952451/ /pubmed/20957128 http://dx.doi.org/10.2147/VHRM.S13368 Text en © 2010 Ditzel and Lervang, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Review
Ditzel, Jørn
Lervang, Hans-Henrik
Lifestyle diseases and cardiovascular risk factors are interrelated to deficiencies of major substrates in ATP synthesis
title Lifestyle diseases and cardiovascular risk factors are interrelated to deficiencies of major substrates in ATP synthesis
title_full Lifestyle diseases and cardiovascular risk factors are interrelated to deficiencies of major substrates in ATP synthesis
title_fullStr Lifestyle diseases and cardiovascular risk factors are interrelated to deficiencies of major substrates in ATP synthesis
title_full_unstemmed Lifestyle diseases and cardiovascular risk factors are interrelated to deficiencies of major substrates in ATP synthesis
title_short Lifestyle diseases and cardiovascular risk factors are interrelated to deficiencies of major substrates in ATP synthesis
title_sort lifestyle diseases and cardiovascular risk factors are interrelated to deficiencies of major substrates in atp synthesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2952451/
https://www.ncbi.nlm.nih.gov/pubmed/20957128
http://dx.doi.org/10.2147/VHRM.S13368
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