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Gene polymorphisms and thyroid function in patients with heart failure

We evaluated nuclear factor kappa B { NFkB , rs28362491 [−94ins/delATTG (W/D)]} and angiotensin converting enzyme { ACE ; rs1799752 [Ins(I)/Del(D)]} gene polymorphisms and their correlation with thyroid function in patients with heart failure (HF). Peak oxygen uptake (VO 2 ) was evaluated (by Weber...

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Published in:Endocrine 2014-02, Vol.45 (1), p.46-54
Main Authors: Vasiliadis, Ioannis, Kolovou, Genovefa, Kolovou, Vana, Giannakopoulou, Vasiliki, Boutsikou, Maria, Katsiki, Niki, Papadopoulou, Evaggelia, Mavrogeni, Sophie, Sorontila, Konstantina, Pantos, Costas, Cokkinos, Dennis V.
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creator Vasiliadis, Ioannis
Kolovou, Genovefa
Kolovou, Vana
Giannakopoulou, Vasiliki
Boutsikou, Maria
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Mavrogeni, Sophie
Sorontila, Konstantina
Pantos, Costas
Cokkinos, Dennis V.
description We evaluated nuclear factor kappa B { NFkB , rs28362491 [−94ins/delATTG (W/D)]} and angiotensin converting enzyme { ACE ; rs1799752 [Ins(I)/Del(D)]} gene polymorphisms and their correlation with thyroid function in patients with heart failure (HF). Peak oxygen uptake (VO 2 ) was evaluated (by Weber classification) during a symptom-limited cardiopulmonary exercise test in 194 patients. Thyroid-stimulating hormone, triiodothyronine (T3), thyroxine (T4), and free (F) T3 and FT4 were also measured. According to their cardiovascular (CV) capacity, patients were subdivided into four groups: group A included patients with peak VO 2 >20 ml/kg/min, group B 16–20 ml/kg/min, group C 10–16 ml/kg/min, and group D 6–10 ml/kg/min. Patients were also genotyped for NFkB and ACE genetic variants. T3 was increased and FT3 was decreased for every raise in Weber’s classification ( p  = 0.007 and p  = 0.012, respectively). Del carriers had elevated FT3 levels compared with Ins carriers ( p  = 0.021). Patients with II genotype had elevated T4 levels compared with ID genotype ( p  = 0.044). Both T4 and FT4 were decreased in D allele carriers ( p  = 0.007 and p  = 0.045, respectively). Thyroid hormones correlated with CV capacity. Associations between the NFkB and ACE gene polymorphisms and thyroid hormones levels were also observed. Further larger studies are required to clarify genes contribution in HF.
doi_str_mv 10.1007/s12020-013-9926-x
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Peak oxygen uptake (VO 2 ) was evaluated (by Weber classification) during a symptom-limited cardiopulmonary exercise test in 194 patients. Thyroid-stimulating hormone, triiodothyronine (T3), thyroxine (T4), and free (F) T3 and FT4 were also measured. According to their cardiovascular (CV) capacity, patients were subdivided into four groups: group A included patients with peak VO 2 &gt;20 ml/kg/min, group B 16–20 ml/kg/min, group C 10–16 ml/kg/min, and group D 6–10 ml/kg/min. Patients were also genotyped for NFkB and ACE genetic variants. T3 was increased and FT3 was decreased for every raise in Weber’s classification ( p  = 0.007 and p  = 0.012, respectively). Del carriers had elevated FT3 levels compared with Ins carriers ( p  = 0.021). Patients with II genotype had elevated T4 levels compared with ID genotype ( p  = 0.044). Both T4 and FT4 were decreased in D allele carriers ( p  = 0.007 and p  = 0.045, respectively). Thyroid hormones correlated with CV capacity. 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Peak oxygen uptake (VO 2 ) was evaluated (by Weber classification) during a symptom-limited cardiopulmonary exercise test in 194 patients. Thyroid-stimulating hormone, triiodothyronine (T3), thyroxine (T4), and free (F) T3 and FT4 were also measured. According to their cardiovascular (CV) capacity, patients were subdivided into four groups: group A included patients with peak VO 2 &gt;20 ml/kg/min, group B 16–20 ml/kg/min, group C 10–16 ml/kg/min, and group D 6–10 ml/kg/min. Patients were also genotyped for NFkB and ACE genetic variants. T3 was increased and FT3 was decreased for every raise in Weber’s classification ( p  = 0.007 and p  = 0.012, respectively). Del carriers had elevated FT3 levels compared with Ins carriers ( p  = 0.021). Patients with II genotype had elevated T4 levels compared with ID genotype ( p  = 0.044). Both T4 and FT4 were decreased in D allele carriers ( p  = 0.007 and p  = 0.045, respectively). Thyroid hormones correlated with CV capacity. Associations between the NFkB and ACE gene polymorphisms and thyroid hormones levels were also observed. Further larger studies are required to clarify genes contribution in HF.</description><subject>Aged</subject><subject>Cohort Studies</subject><subject>Diabetes</subject><subject>Endocrinology</subject><subject>Female</subject><subject>Genotype</subject><subject>Heart Failure - blood</subject><subject>Heart Failure - genetics</subject><subject>Heart Failure - physiopathology</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Middle Aged</subject><subject>multidisciplinary</subject><subject>NF-kappa B p50 Subunit - genetics</subject><subject>Original Article</subject><subject>Peptidyl-Dipeptidase A - genetics</subject><subject>Polymorphism, Genetic</subject><subject>Science</subject><subject>Thyroid Function Tests</subject><subject>Thyroid Gland - physiology</subject><subject>Thyrotropin - blood</subject><subject>Thyroxine - blood</subject><subject>Triiodothyronine - blood</subject><issn>1355-008X</issn><issn>1559-0100</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9kEtPwzAQhC0EoqXwA7ggH7kE1q88jqiiBQmJC0jcLDexiavECXYi2n-PqxSOnHa1OzPSfAhdE7gjANl9IBQoJEBYUhQ0TXYnaE6EKOIF4DTuTIgEIP-YoYsQtgCU0jQ7RzPKBGecsTlarbXTuO-afdv5vrahDVi5Cg_13ne2wmZ05WA7h63DvRqsdkPA33aoca2VH7BRthm9vkRnRjVBXx3nAr2vHt-WT8nL6_p5-fCSlIzzIcmIBiayiqc5A855YUxuhKDpJiOMMAZQMihNSbRQGd9wozJhCpMXeSyqBWELdDvl9r77GnUYZGtDqZtGOd2NQRJesByIYGmUkkla-i4Er43svW2V30sC8oBPTvhkxCcP-OQuem6O8eOm1dWf45dXFNBJEOLLfWovt93oXaz8T-oPN5R6Wg</recordid><startdate>20140201</startdate><enddate>20140201</enddate><creator>Vasiliadis, Ioannis</creator><creator>Kolovou, Genovefa</creator><creator>Kolovou, Vana</creator><creator>Giannakopoulou, Vasiliki</creator><creator>Boutsikou, Maria</creator><creator>Katsiki, Niki</creator><creator>Papadopoulou, Evaggelia</creator><creator>Mavrogeni, Sophie</creator><creator>Sorontila, Konstantina</creator><creator>Pantos, Costas</creator><creator>Cokkinos, Dennis V.</creator><general>Springer US</general><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>20140201</creationdate><title>Gene polymorphisms and thyroid function in patients with heart failure</title><author>Vasiliadis, Ioannis ; 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rs1799752 [Ins(I)/Del(D)]} gene polymorphisms and their correlation with thyroid function in patients with heart failure (HF). Peak oxygen uptake (VO 2 ) was evaluated (by Weber classification) during a symptom-limited cardiopulmonary exercise test in 194 patients. Thyroid-stimulating hormone, triiodothyronine (T3), thyroxine (T4), and free (F) T3 and FT4 were also measured. According to their cardiovascular (CV) capacity, patients were subdivided into four groups: group A included patients with peak VO 2 &gt;20 ml/kg/min, group B 16–20 ml/kg/min, group C 10–16 ml/kg/min, and group D 6–10 ml/kg/min. Patients were also genotyped for NFkB and ACE genetic variants. T3 was increased and FT3 was decreased for every raise in Weber’s classification ( p  = 0.007 and p  = 0.012, respectively). Del carriers had elevated FT3 levels compared with Ins carriers ( p  = 0.021). Patients with II genotype had elevated T4 levels compared with ID genotype ( p  = 0.044). Both T4 and FT4 were decreased in D allele carriers ( p  = 0.007 and p  = 0.045, respectively). Thyroid hormones correlated with CV capacity. Associations between the NFkB and ACE gene polymorphisms and thyroid hormones levels were also observed. Further larger studies are required to clarify genes contribution in HF.</abstract><cop>Boston</cop><pub>Springer US</pub><pmid>23543433</pmid><doi>10.1007/s12020-013-9926-x</doi><tpages>9</tpages></addata></record>
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subjects Aged
Cohort Studies
Diabetes
Endocrinology
Female
Genotype
Heart Failure - blood
Heart Failure - genetics
Heart Failure - physiopathology
Humanities and Social Sciences
Humans
Internal Medicine
Male
Medicine
Medicine & Public Health
Middle Aged
multidisciplinary
NF-kappa B p50 Subunit - genetics
Original Article
Peptidyl-Dipeptidase A - genetics
Polymorphism, Genetic
Science
Thyroid Function Tests
Thyroid Gland - physiology
Thyrotropin - blood
Thyroxine - blood
Triiodothyronine - blood
title Gene polymorphisms and thyroid function in patients with heart failure
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