Hypomagnesemia, oxidative stress, inflammation, and metabolic syndrome

Background Although hypomagnesemia, oxidative stress, and inflammation are involved in the pathogenesis of cardiovascular diseases, there is not a previous description concerning their potential interaction; thus, the aim of this study was to examine the relationship between metabolic syndrome (MetS...

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Veröffentlicht in:Diabetes/metabolism research and reviews 2006-11, Vol.22 (6), p.471-476
Hauptverfasser: Guerrero-Romero, Fernando, Rodríguez-Morán, Martha
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Rodríguez-Morán, Martha
description Background Although hypomagnesemia, oxidative stress, and inflammation are involved in the pathogenesis of cardiovascular diseases, there is not a previous description concerning their potential interaction; thus, the aim of this study was to examine the relationship between metabolic syndrome (MetS), hypomagnesemia, inflammation, and oxidative stress. Methods Case‐control design study. Incident cases of MetS (84 women and 63 men) were compared with healthy control subjects (163 women and 131 men) matched by age and gender. MetS was diagnosed according to the Adult Treatment Panel III (ATP III) criterion. Oxidative stress was defined by serum malondialdehyde concentration (MDA) ≥50 mg/dL, low‐grade chronic inflammation by C‐reactive protein (CRP) serum levels ≥3 mg/L, and hypomagnesemia by serum magnesium concentrations ≤1.8 mg/dL. Results Multivariate analysis adjusted by age, sex, body mass index, waist‐to‐hip ratio, and total adiposity showed a strong association between MetS and hypomagnesemia (OR 1.9; 95% CI 1.3–7.1), inflammation (OR 1.7; 95% CI 1.4–8.4), and oxidative stress (OR 1.4; 95% CI 0.9–12.6). Additional adjustment by CRP levels showed that MetS remained associated to hypomagnesemia (OR 1.4; 95% CI 1.1–5.9) but not to oxidative stress (OR 1.1; 95% CI 0.9–5.9), and adjusted by MDA levels, MetS remained strongly associated to hypomagnesemia (1.6; CI 95% 1.1–7.4), but not to inflammation (OR 1.05; 95% CI 0.97–14.2). Adjusted by serum magnesium levels, inflammation (OR 1.2; 95% CI 1.1–9.1) and oxidative stress (OR 1.1; 95% CI 1.1–9.7) were slightly associated to MetS. Conclusions The interaction of inflammation and oxidative stress is related and increases the risk for MetS, whereas serum magnesium levels and MetS are independently associated. Copyright © 2006 John Wiley & Sons, Ltd.
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Methods Case‐control design study. Incident cases of MetS (84 women and 63 men) were compared with healthy control subjects (163 women and 131 men) matched by age and gender. MetS was diagnosed according to the Adult Treatment Panel III (ATP III) criterion. Oxidative stress was defined by serum malondialdehyde concentration (MDA) ≥50 mg/dL, low‐grade chronic inflammation by C‐reactive protein (CRP) serum levels ≥3 mg/L, and hypomagnesemia by serum magnesium concentrations ≤1.8 mg/dL. Results Multivariate analysis adjusted by age, sex, body mass index, waist‐to‐hip ratio, and total adiposity showed a strong association between MetS and hypomagnesemia (OR 1.9; 95% CI 1.3–7.1), inflammation (OR 1.7; 95% CI 1.4–8.4), and oxidative stress (OR 1.4; 95% CI 0.9–12.6). Additional adjustment by CRP levels showed that MetS remained associated to hypomagnesemia (OR 1.4; 95% CI 1.1–5.9) but not to oxidative stress (OR 1.1; 95% CI 0.9–5.9), and adjusted by MDA levels, MetS remained strongly associated to hypomagnesemia (1.6; CI 95% 1.1–7.4), but not to inflammation (OR 1.05; 95% CI 0.97–14.2). Adjusted by serum magnesium levels, inflammation (OR 1.2; 95% CI 1.1–9.1) and oxidative stress (OR 1.1; 95% CI 1.1–9.7) were slightly associated to MetS. Conclusions The interaction of inflammation and oxidative stress is related and increases the risk for MetS, whereas serum magnesium levels and MetS are independently associated. 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Res. Rev</addtitle><description>Background Although hypomagnesemia, oxidative stress, and inflammation are involved in the pathogenesis of cardiovascular diseases, there is not a previous description concerning their potential interaction; thus, the aim of this study was to examine the relationship between metabolic syndrome (MetS), hypomagnesemia, inflammation, and oxidative stress. Methods Case‐control design study. Incident cases of MetS (84 women and 63 men) were compared with healthy control subjects (163 women and 131 men) matched by age and gender. MetS was diagnosed according to the Adult Treatment Panel III (ATP III) criterion. Oxidative stress was defined by serum malondialdehyde concentration (MDA) ≥50 mg/dL, low‐grade chronic inflammation by C‐reactive protein (CRP) serum levels ≥3 mg/L, and hypomagnesemia by serum magnesium concentrations ≤1.8 mg/dL. Results Multivariate analysis adjusted by age, sex, body mass index, waist‐to‐hip ratio, and total adiposity showed a strong association between MetS and hypomagnesemia (OR 1.9; 95% CI 1.3–7.1), inflammation (OR 1.7; 95% CI 1.4–8.4), and oxidative stress (OR 1.4; 95% CI 0.9–12.6). Additional adjustment by CRP levels showed that MetS remained associated to hypomagnesemia (OR 1.4; 95% CI 1.1–5.9) but not to oxidative stress (OR 1.1; 95% CI 0.9–5.9), and adjusted by MDA levels, MetS remained strongly associated to hypomagnesemia (1.6; CI 95% 1.1–7.4), but not to inflammation (OR 1.05; 95% CI 0.97–14.2). Adjusted by serum magnesium levels, inflammation (OR 1.2; 95% CI 1.1–9.1) and oxidative stress (OR 1.1; 95% CI 1.1–9.7) were slightly associated to MetS. Conclusions The interaction of inflammation and oxidative stress is related and increases the risk for MetS, whereas serum magnesium levels and MetS are independently associated. Copyright © 2006 John Wiley &amp; Sons, Ltd.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>C-reactive protein</subject><subject>C-Reactive Protein - metabolism</subject><subject>Case-Control Studies</subject><subject>Diabetes. Impaired glucose tolerance</subject><subject>Endocrine pancreas. Apud cells (diseases)</subject><subject>Endocrinopathies</subject><subject>Etiopathogenesis. Screening. Investigations. Target tissue resistance</subject><subject>Female</subject><subject>Humans</subject><subject>hypomagnesemia</subject><subject>inflammation</subject><subject>Inflammation - physiopathology</subject><subject>Logistic Models</subject><subject>Magnesium - blood</subject><subject>Male</subject><subject>malondialdehyde</subject><subject>Malondialdehyde - blood</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>metabolic syndrome</subject><subject>Metabolic Syndrome - physiopathology</subject><subject>Metals (hemochromatosis...)</subject><subject>Middle Aged</subject><subject>Other metabolic disorders</subject><subject>oxidative stress</subject><subject>Oxidative Stress - physiology</subject><subject>Risk</subject><issn>1520-7552</issn><issn>1520-7560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10E1P2zAYwHELbaKFTeIToFw2cWiYHb_FR1QoMHWdVG30aDnOE2SIk85OgX57UjUqp51sWT89j_VH6IzgS4Jx9qP0IVwKxo7QmPAMp5IL_Olw59kIncT4hDGmTLBjNCKCq1yofIxmd9t1681jAxG8M5OkfXOl6dwLJLELEOMkcU1VG-_7x7aZJKYpEw-dKdra2SRumzK0Hr6gz5WpI3wdzlP0d3bzZ3qXzn_f3k-v5qmlVLCUcWAZlgZXnCtsWf9PypQqlSQFJxZjllkprMozRaW1FnihWAZQ4LwiUuT0FH3fz12H9t8GYqe9ixbq2jTQbqIWuVJE0B282EMb2hgDVHodnDdhqwnWu2Z610z3zXp6PszcFB7KDzhE6sG3AZhoTV0F01gXP1ye9Z2p6l26d6-uhu1_F-rrX8vlfvHgXezg7eBNeNZCUsn1anGrFw-rGZ3Kn3pJ3wHUy5FK</recordid><startdate>200611</startdate><enddate>200611</enddate><creator>Guerrero-Romero, Fernando</creator><creator>Rodríguez-Morán, Martha</creator><general>John Wiley &amp; Sons, Ltd</general><general>Wiley</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200611</creationdate><title>Hypomagnesemia, oxidative stress, inflammation, and metabolic syndrome</title><author>Guerrero-Romero, Fernando ; Rodríguez-Morán, Martha</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3364-45e4207a0f5590c47563499d971b51c0042c76c982937ccce5b942eeb08f17683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>C-reactive protein</topic><topic>C-Reactive Protein - metabolism</topic><topic>Case-Control Studies</topic><topic>Diabetes. Impaired glucose tolerance</topic><topic>Endocrine pancreas. Apud cells (diseases)</topic><topic>Endocrinopathies</topic><topic>Etiopathogenesis. Screening. Investigations. Target tissue resistance</topic><topic>Female</topic><topic>Humans</topic><topic>hypomagnesemia</topic><topic>inflammation</topic><topic>Inflammation - physiopathology</topic><topic>Logistic Models</topic><topic>Magnesium - blood</topic><topic>Male</topic><topic>malondialdehyde</topic><topic>Malondialdehyde - blood</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>metabolic syndrome</topic><topic>Metabolic Syndrome - physiopathology</topic><topic>Metals (hemochromatosis...)</topic><topic>Middle Aged</topic><topic>Other metabolic disorders</topic><topic>oxidative stress</topic><topic>Oxidative Stress - physiology</topic><topic>Risk</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guerrero-Romero, Fernando</creatorcontrib><creatorcontrib>Rodríguez-Morán, Martha</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Diabetes/metabolism research and reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guerrero-Romero, Fernando</au><au>Rodríguez-Morán, Martha</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypomagnesemia, oxidative stress, inflammation, and metabolic syndrome</atitle><jtitle>Diabetes/metabolism research and reviews</jtitle><addtitle>Diabetes Metab. Res. Rev</addtitle><date>2006-11</date><risdate>2006</risdate><volume>22</volume><issue>6</issue><spage>471</spage><epage>476</epage><pages>471-476</pages><issn>1520-7552</issn><eissn>1520-7560</eissn><coden>DMRRFM</coden><abstract>Background Although hypomagnesemia, oxidative stress, and inflammation are involved in the pathogenesis of cardiovascular diseases, there is not a previous description concerning their potential interaction; thus, the aim of this study was to examine the relationship between metabolic syndrome (MetS), hypomagnesemia, inflammation, and oxidative stress. Methods Case‐control design study. Incident cases of MetS (84 women and 63 men) were compared with healthy control subjects (163 women and 131 men) matched by age and gender. MetS was diagnosed according to the Adult Treatment Panel III (ATP III) criterion. Oxidative stress was defined by serum malondialdehyde concentration (MDA) ≥50 mg/dL, low‐grade chronic inflammation by C‐reactive protein (CRP) serum levels ≥3 mg/L, and hypomagnesemia by serum magnesium concentrations ≤1.8 mg/dL. Results Multivariate analysis adjusted by age, sex, body mass index, waist‐to‐hip ratio, and total adiposity showed a strong association between MetS and hypomagnesemia (OR 1.9; 95% CI 1.3–7.1), inflammation (OR 1.7; 95% CI 1.4–8.4), and oxidative stress (OR 1.4; 95% CI 0.9–12.6). Additional adjustment by CRP levels showed that MetS remained associated to hypomagnesemia (OR 1.4; 95% CI 1.1–5.9) but not to oxidative stress (OR 1.1; 95% CI 0.9–5.9), and adjusted by MDA levels, MetS remained strongly associated to hypomagnesemia (1.6; CI 95% 1.1–7.4), but not to inflammation (OR 1.05; 95% CI 0.97–14.2). Adjusted by serum magnesium levels, inflammation (OR 1.2; 95% CI 1.1–9.1) and oxidative stress (OR 1.1; 95% CI 1.1–9.7) were slightly associated to MetS. Conclusions The interaction of inflammation and oxidative stress is related and increases the risk for MetS, whereas serum magnesium levels and MetS are independently associated. Copyright © 2006 John Wiley &amp; Sons, Ltd.</abstract><cop>Chichester, UK</cop><pub>John Wiley &amp; Sons, Ltd</pub><pmid>16598698</pmid><doi>10.1002/dmrr.644</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Biological and medical sciences
C-reactive protein
C-Reactive Protein - metabolism
Case-Control Studies
Diabetes. Impaired glucose tolerance
Endocrine pancreas. Apud cells (diseases)
Endocrinopathies
Etiopathogenesis. Screening. Investigations. Target tissue resistance
Female
Humans
hypomagnesemia
inflammation
Inflammation - physiopathology
Logistic Models
Magnesium - blood
Male
malondialdehyde
Malondialdehyde - blood
Medical sciences
Metabolic diseases
metabolic syndrome
Metabolic Syndrome - physiopathology
Metals (hemochromatosis...)
Middle Aged
Other metabolic disorders
oxidative stress
Oxidative Stress - physiology
Risk
title Hypomagnesemia, oxidative stress, inflammation, and metabolic syndrome
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