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Renal impairment and heart failure with preserved ejection fraction early post-myocardial infarction

Identifieur interne : 002483 ( Pmc/Checkpoint ); précédent : 002482; suivant : 002484

Renal impairment and heart failure with preserved ejection fraction early post-myocardial infarction

Auteurs : Vinod Jorapur ; Gervasio A. Lamas ; Zygmunt P. Sadowski ; Harmony R. Reynolds ; Antonio C. Carvalho ; Christopher E. Buller ; James M. Rankin ; Jean Renkin ; Philippe Gabriel Steg ; Harvey D. White ; Carlos Vozzi ; Eduardo Balcells ; Michael Ragosta ; C Edwin Martin ; Vankeepuram S. Srinivas ; William W. Wharton Iii ; Staci Abramsky ; Ana C. Mon ; Shari S. Kronsberg ; Judith S. Hochman

Source :

RBID : PMC:2946261

Abstract

AIM: To study if impaired renal function is associated with increased risk of peri-infarct heart failure (HF) in patients with preserved ejection fraction (EF).

METHODS: Patients with occluded infarct-related arteries (IRAs) between 1 to 28 d after myocardial infarction (MI) were grouped into chronic kidney disease (CKD) stages based on estimated glomerular filtration rate (eGFR). Rates of early post-MI HF were compared among eGFR groups. Logistic regression was used to explore independent predictors of HF.

RESULTS: Reduced eGFR was present in 71.1% of 2160 patients, with significant renal impairment (eGFR < 60 mL/min every 1.73 m2) in 14.8%. The prevalence of HF was higher with worsening renal function: 15.5%, 17.8% and 29.4% in patients with CKD stages 1, 2 and 3 or 4, respectively (P < 0.0001), despite a small absolute difference in mean EF across eGFR groups: 48.2 ± 10.0, 47.9 ± 11.3 and 46.2 ± 12.1, respectively (P = 0.02). The prevalence of HF was again higher with worsening renal function among patients with preserved EF: 10.1%, 13.6% and 23.6% (P < 0.0001), but this relationship was not significant among patients with depressed EF: 27.1%, 26.2% and 37.9% (P = 0.071). Moreover, eGFR was an independent correlate of HF in patients with preserved EF (P = 0.003) but not in patients with depressed EF (P = 0.181).

CONCLUSION: A significant proportion of post-MI patients with occluded IRAs have impaired renal function. Impaired renal function was associated with an increased rate of early post-MI HF, the association being strongest in patients with preserved EF. These findings have implications for management of peri-infarct HF.


Url:
DOI: 10.4330/wjc.v2.i1.13
PubMed: 20885993
PubMed Central: 2946261


Affiliations:


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<title level="j">World Journal of Cardiology</title>
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<div type="abstract" xml:lang="en">
<p>AIM: To study if impaired renal function is associated with increased risk of peri-infarct heart failure (HF) in patients with preserved ejection fraction (EF).</p>
<p>METHODS: Patients with occluded infarct-related arteries (IRAs) between 1 to 28 d after myocardial infarction (MI) were grouped into chronic kidney disease (CKD) stages based on estimated glomerular filtration rate (eGFR). Rates of early post-MI HF were compared among eGFR groups. Logistic regression was used to explore independent predictors of HF.</p>
<p>RESULTS: Reduced eGFR was present in 71.1% of 2160 patients, with significant renal impairment (eGFR < 60 mL/min every 1.73 m
<sup>2</sup>
) in 14.8%. The prevalence of HF was higher with worsening renal function: 15.5%, 17.8% and 29.4% in patients with CKD stages 1, 2 and 3 or 4, respectively (
<italic>P</italic>
< 0.0001), despite a small absolute difference in mean EF across eGFR groups: 48.2 ± 10.0, 47.9 ± 11.3 and 46.2 ± 12.1, respectively (
<italic>P</italic>
= 0.02). The prevalence of HF was again higher with worsening renal function among patients with preserved EF: 10.1%, 13.6% and 23.6% (
<italic>P</italic>
< 0.0001), but this relationship was not significant among patients with depressed EF: 27.1%, 26.2% and 37.9% (
<italic>P</italic>
= 0.071). Moreover, eGFR was an independent correlate of HF in patients with preserved EF (
<italic>P</italic>
= 0.003) but not in patients with depressed EF (
<italic>P</italic>
= 0.181).</p>
<p>CONCLUSION: A significant proportion of post-MI patients with occluded IRAs have impaired renal function. Impaired renal function was associated with an increased rate of early post-MI HF, the association being strongest in patients with preserved EF. These findings have implications for management of peri-infarct HF.</p>
</div>
</front>
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<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">World J Cardiol</journal-id>
<journal-id journal-id-type="publisher-id">WJC</journal-id>
<journal-title-group>
<journal-title>World Journal of Cardiology</journal-title>
</journal-title-group>
<issn pub-type="ppub">1949-8462</issn>
<issn pub-type="epub">1949-8462</issn>
<publisher>
<publisher-name>Baishideng Publishing Group Co., Limited</publisher-name>
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<article-id pub-id-type="pmid">20885993</article-id>
<article-id pub-id-type="pmc">2946261</article-id>
<article-id pub-id-type="other">jWJC.v2.i1.pg13</article-id>
<article-id pub-id-type="doi">10.4330/wjc.v2.i1.13</article-id>
<article-categories>
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<subject>Brief Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Renal impairment and heart failure with preserved ejection fraction early post-myocardial infarction</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Jorapur</surname>
<given-names>Vinod</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Lamas</surname>
<given-names>Gervasio A</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Sadowski</surname>
<given-names>Zygmunt P</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Reynolds</surname>
<given-names>Harmony R</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Carvalho</surname>
<given-names>Antonio C</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Buller</surname>
<given-names>Christopher E</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Rankin</surname>
<given-names>James M</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Renkin</surname>
<given-names>Jean</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Steg</surname>
<given-names>Philippe Gabriel</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>White</surname>
<given-names>Harvey D</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Vozzi</surname>
<given-names>Carlos</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Balcells</surname>
<given-names>Eduardo</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ragosta</surname>
<given-names>Michael</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Martin</surname>
<given-names>C Edwin</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Srinivas</surname>
<given-names>Vankeepuram S</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Wharton III</surname>
<given-names>William W</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Abramsky</surname>
<given-names>Staci</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Mon</surname>
<given-names>Ana C</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kronsberg</surname>
<given-names>Shari S</given-names>
</name>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Hochman</surname>
<given-names>Judith S</given-names>
</name>
</contrib>
<aff>Vinod Jorapur, Gervasio A Lamas, Ana C Mon, Columbia University Division of Cardiology, Mount Sinai Medical Center, Miami Beach, FL 33140, United States</aff>
<aff>Zygmunt P Sadowski, II Ischemic Heart Disease Department, National Institute of Cardiology, Warsaw, 04628, Poland</aff>
<aff>Harmony R Reynolds, Staci Abramsky, Judith S Hochman, Leon Charney Division of Cardiology, New York University School of Medicine, NY 10016, United States</aff>
<aff>Antonio C Carvalho, Cardiology Division - Hospital Sao Paulo, Federal University of Sao Paulo, Sao Paulo, 04080004, Brazil</aff>
<aff>Christopher E Buller, Division of Cardiology, University of British Columbia, Vancouver, British Columbia, L8L 2X2, Canada</aff>
<aff>James M Rankin, Department of Cardiovascular Medicine, Royal Perth Hospital, Perth 6000, Australia</aff>
<aff>Jean Renkin, Department of Cardiology, UCL St Luc University Hospital, Brussels 1200, Belgium</aff>
<aff>Philippe Gabriel Steg, INSERM U-698, Department of Cardiology, Hopital Bichat, AP-HP, and Université Paris 7, Paris 75877, France</aff>
<aff>Harvey D White, Cardiology Department, Green Lane Cardiovascular Service, Auckland City Hospital, Auckland 1142, New Zealand</aff>
<aff>Carlos Vozzi, Interventional Cardiology, Instituto de Intervenciones Cardiovasculares S.A., Rosario 2000, Argentina</aff>
<aff>Eduardo Balcells, Cardiovascular Associates, Wellmont Holston Valley Medical Center, Kingsport, TN 37660, United States</aff>
<aff>Michael Ragosta, Cardiovascular Division, University of Virginia, Charlottesville, VA 22908, United States</aff>
<aff>C Edwin Martin, Department of Medicine - Division of Cardiology, York Hospital, York, PA 17405, United States</aff>
<aff>Vankeepuram S Srinivas, Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY 10468, United States</aff>
<aff>William W Wharton III, Research Department, Asheville Cardiology Associates, P.A., Asheville, NC 28803, United States</aff>
<aff>Shari S Kronsberg, Maryland Medical Research Institute, Baltimore, MD 21210, United States</aff>
</contrib-group>
<author-notes>
<fn>
<p>Author contributions: The authors had full access to the data and take responsibility for its integrity; all authors have read and agree to the manuscript as written.</p>
<p>Correspondence to: Judith S Hochman, MD, Leon Charney Division of Cardiology, New York University School of Medicine, NY 10016, United States.
<email>judith.hochman@nyumc.org</email>
</p>
<p>Telephone: +1-212-2636927 Fax: +1-212-2637129</p>
</fn>
</author-notes>
<pub-date pub-type="ppub">
<day>26</day>
<month>1</month>
<year>2010</year>
</pub-date>
<pub-date pub-type="epub">
<day>26</day>
<month>1</month>
<year>2010</year>
</pub-date>
<volume>2</volume>
<issue>1</issue>
<fpage>13</fpage>
<lpage>18</lpage>
<history>
<date date-type="received">
<day>16</day>
<month>1</month>
<year>2010</year>
</date>
<date date-type="rev-recd">
<day>24</day>
<month>1</month>
<year>2010</year>
</date>
<date date-type="accepted">
<day>25</day>
<month>1</month>
<year>2010</year>
</date>
</history>
<permissions>
<copyright-statement>©2010 Baishideng Publishing Group Co., Limited. All rights reserved.</copyright-statement>
<copyright-year>2010</copyright-year>
</permissions>
<abstract>
<p>AIM: To study if impaired renal function is associated with increased risk of peri-infarct heart failure (HF) in patients with preserved ejection fraction (EF).</p>
<p>METHODS: Patients with occluded infarct-related arteries (IRAs) between 1 to 28 d after myocardial infarction (MI) were grouped into chronic kidney disease (CKD) stages based on estimated glomerular filtration rate (eGFR). Rates of early post-MI HF were compared among eGFR groups. Logistic regression was used to explore independent predictors of HF.</p>
<p>RESULTS: Reduced eGFR was present in 71.1% of 2160 patients, with significant renal impairment (eGFR < 60 mL/min every 1.73 m
<sup>2</sup>
) in 14.8%. The prevalence of HF was higher with worsening renal function: 15.5%, 17.8% and 29.4% in patients with CKD stages 1, 2 and 3 or 4, respectively (
<italic>P</italic>
< 0.0001), despite a small absolute difference in mean EF across eGFR groups: 48.2 ± 10.0, 47.9 ± 11.3 and 46.2 ± 12.1, respectively (
<italic>P</italic>
= 0.02). The prevalence of HF was again higher with worsening renal function among patients with preserved EF: 10.1%, 13.6% and 23.6% (
<italic>P</italic>
< 0.0001), but this relationship was not significant among patients with depressed EF: 27.1%, 26.2% and 37.9% (
<italic>P</italic>
= 0.071). Moreover, eGFR was an independent correlate of HF in patients with preserved EF (
<italic>P</italic>
= 0.003) but not in patients with depressed EF (
<italic>P</italic>
= 0.181).</p>
<p>CONCLUSION: A significant proportion of post-MI patients with occluded IRAs have impaired renal function. Impaired renal function was associated with an increased rate of early post-MI HF, the association being strongest in patients with preserved EF. These findings have implications for management of peri-infarct HF.</p>
</abstract>
<kwd-group>
<kwd>Heart failure</kwd>
<kwd>Myocardial infarction</kwd>
<kwd>Kidney disease</kwd>
</kwd-group>
</article-meta>
</front>
</pmc>
<affiliations>
<list></list>
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<name sortKey="Abramsky, Staci" sort="Abramsky, Staci" uniqKey="Abramsky S" first="Staci" last="Abramsky">Staci Abramsky</name>
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<name sortKey="Buller, Christopher E" sort="Buller, Christopher E" uniqKey="Buller C" first="Christopher E" last="Buller">Christopher E. Buller</name>
<name sortKey="Carvalho, Antonio C" sort="Carvalho, Antonio C" uniqKey="Carvalho A" first="Antonio C" last="Carvalho">Antonio C. Carvalho</name>
<name sortKey="Hochman, Judith S" sort="Hochman, Judith S" uniqKey="Hochman J" first="Judith S" last="Hochman">Judith S. Hochman</name>
<name sortKey="Jorapur, Vinod" sort="Jorapur, Vinod" uniqKey="Jorapur V" first="Vinod" last="Jorapur">Vinod Jorapur</name>
<name sortKey="Kronsberg, Shari S" sort="Kronsberg, Shari S" uniqKey="Kronsberg S" first="Shari S" last="Kronsberg">Shari S. Kronsberg</name>
<name sortKey="Lamas, Gervasio A" sort="Lamas, Gervasio A" uniqKey="Lamas G" first="Gervasio A" last="Lamas">Gervasio A. Lamas</name>
<name sortKey="Martin, C Edwin" sort="Martin, C Edwin" uniqKey="Martin C" first="C Edwin" last="Martin">C Edwin Martin</name>
<name sortKey="Mon, Ana C" sort="Mon, Ana C" uniqKey="Mon A" first="Ana C" last="Mon">Ana C. Mon</name>
<name sortKey="Ragosta, Michael" sort="Ragosta, Michael" uniqKey="Ragosta M" first="Michael" last="Ragosta">Michael Ragosta</name>
<name sortKey="Rankin, James M" sort="Rankin, James M" uniqKey="Rankin J" first="James M" last="Rankin">James M. Rankin</name>
<name sortKey="Renkin, Jean" sort="Renkin, Jean" uniqKey="Renkin J" first="Jean" last="Renkin">Jean Renkin</name>
<name sortKey="Reynolds, Harmony R" sort="Reynolds, Harmony R" uniqKey="Reynolds H" first="Harmony R" last="Reynolds">Harmony R. Reynolds</name>
<name sortKey="Sadowski, Zygmunt P" sort="Sadowski, Zygmunt P" uniqKey="Sadowski Z" first="Zygmunt P" last="Sadowski">Zygmunt P. Sadowski</name>
<name sortKey="Srinivas, Vankeepuram S" sort="Srinivas, Vankeepuram S" uniqKey="Srinivas V" first="Vankeepuram S" last="Srinivas">Vankeepuram S. Srinivas</name>
<name sortKey="Steg, Philippe Gabriel" sort="Steg, Philippe Gabriel" uniqKey="Steg P" first="Philippe Gabriel" last="Steg">Philippe Gabriel Steg</name>
<name sortKey="Vozzi, Carlos" sort="Vozzi, Carlos" uniqKey="Vozzi C" first="Carlos" last="Vozzi">Carlos Vozzi</name>
<name sortKey="Wharton Iii, William W" sort="Wharton Iii, William W" uniqKey="Wharton Iii W" first="William W" last="Wharton Iii">William W. Wharton Iii</name>
<name sortKey="White, Harvey D" sort="White, Harvey D" uniqKey="White H" first="Harvey D" last="White">Harvey D. White</name>
</noCountry>
</tree>
</affiliations>
</record>

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