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NR7958

Genetic basis of syndrome MIA (Malnutrition - Inflammation - Atherosclerosis) - complication of hemodialysis treatment

Public support

  • Provider

    Ministry of Health

  • Programme

    Branch programm of research of the Ministry of Health

  • Call for proposals

    VaV pro Ministerstvo zdravotnictví 1 (SMZ02004NR)

  • Main participants

  • Contest type

    VS - Public tender

  • Contract ID

    NR7958-5/2004

Alternative language

  • Project name in Czech

    Genetická podstata komplikace hemodialyzační léčby - syndromu MIA (Malnutrition-Inflammation-Atherosclerosis)

  • Annotation in Czech

    Charakterizovat na pacientech s chronickým renálním selháním a MIA syndromem frekvence alel a genotypů genů pro ghrelin, LBP a HFE a zjistit, zda se liší od výskytu alel v populaci. Zjistit, jak varianty genů pro ghrelin, LBP a HFE ovlivní komplikace hemodialyzační léčby a incidenci kardiovaskulárních onemocnění u pacientů s chronickým renálním selháním a MIA syndromem.

Scientific branches

  • R&D category

    NV - Nonindustrial research (Applied research excluded Industrial research)

  • CEP classification - main branch

    EB - Genetics and molecular biology

  • CEP - secondary branch

    FA - Cardiovascular diseases including cardio-surgery

  • CEP - another secondary branch

    FB - Endocrinology, diabetology, metabolism, nutrition

  • OECD FORD - equivalent branches <br>(according to the <a href="http://www.vyzkum.cz/storage/att/E6EF7938F0E854BAE520AC119FB22E8D/Prevodnik_oboru_Frascati.pdf">converter</a>)

    10603 - Genetics and heredity (medical genetics to be 3)<br>10604 - Reproductive biology (medical aspects to be 3)<br>10605 - Developmental biology<br>10608 - Biochemistry and molecular biology<br>10609 - Biochemical research methods<br>30101 - Human genetics<br>30201 - Cardiac and Cardiovascular systems<br>30202 - Endocrinology and metabolism (including diabetes, hormones)

Completed project evaluation

  • Provider evaluation

    V - Vynikající výsledky projektu (s mezinárodním významem atd.)

  • Project results evaluation

    Altogether 16 variants in 8 genes were analyzed as putative risk factors for renal failure and/or hemodialysis complications. Renal failure was associated with variants APOE, HFE, FTO, MTHFR. Ghrelin variants had effect on cholesterol a BMI development.

Solution timeline

  • Realization period - beginning

    Jan 1, 2004

  • Realization period - end

    Dec 31, 2008

  • Project status

    U - Finished project

  • Latest support payment

    Mar 5, 2008

Data delivery to CEP

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

  • Data delivery code

    CEP09-MZ0-NR-U/09:2

  • Data delivery date

    Apr 27, 2011

Finance

  • Total approved costs

    4,136 thou. CZK

  • Public financial support

    3,810 thou. CZK

  • Other public sources

    131 thou. CZK

  • Non public and foreign sources

    0 thou. CZK