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Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B.

Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. Research Abstract Details 

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  • Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. Abstract Text:

    vikki g nolanVikki G Nolan,qianli maQianli Ma,herbert t cohenHerbert T Cohen,adeboye adewoyeAdeboye Adewoye,anne c rybickiAnne C Rybicki,clinton baldwinClinton Baldwin,rhea n mahabirRhea N Mahabir,erica p homanErica P Homan,diego f wyszynskiDiego F Wyszynski,mary e fabryMary E Fabry,ronald l nagelRonald L Nagel,lindsay a farrerLindsay A Farrer,martin h steinbergMartin H Steinberg,

    Renal disease is common in sickle cell anemia. In this exploratory work, we used data from a longitudinal study of the natural history of sickle cell disease to examine the hypothesis that polymorphisms (SNPs) in selected candidate genes are associated with glomerular filtration rate (GFR). DNA samples and clinical and laboratory data were available for 1,140 patients with sickle cell anemia. GFR was estimated using the Cockcroft-Gault and Schwartz formulas for adults and children, respectively. We examined approximately 175 haplotype tagging (ht) SNPs in about 70 genes of the TGFbeta/BMP pathway for their association with GFR using linear regression. Four SNPs in BMPR1B, a bone morphogenetic protein (BMP) receptor gene, yielded statistically significant associations (P values ranging from 0.015 to 0.046). Three haplotypes in this gene were also associated with GFR. The TGF-beta/BMP pathway has been associated with the development of diabetic nephropathy, which has some features in common with sickle cell nephropathy. Our results suggest that, as with other subphenotypes of sickle cell disease, renal function may be genetically modulated.

    Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. Publishing Authors By Initials

    vg nolanVG Nolan,q maQ Ma,ht cohenHT Cohen,a adewoyeA Adewoye,ac rybickiAC Rybicki,c baldwinC Baldwin,rn mahabirRN Mahabir,ep homanEP Homan,df wyszynskiDF Wyszynski,me fabryME Fabry,rl nagelRL Nagel,la farrerLA Farrer,mh steinbergMH Steinberg,

    For similar genetic phenomena: variation (genetics): polymorphism, genetic: polymorphism, single nucleotide research abstracts see: genetic phenomena: variation (genetics): polymorphism, genetic: polymorphism, single nucleotide research

    PUBMED ID PMID:

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    Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: American journal of hematology

    VOLUME: 82

    Page Numbers: 179-84

    Journal Abbreviation: Am. J. Hematol.

    ISSN: 0361-8609

    DAY: 3

    MONTH: Mar

    YEAR: 2007

    Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 7610369

    Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. Keywords Mesh Terms:

    KEYWORDS: Polymorphism, Single Nucleotide

    MESH TERMS: genetics

    Chemical & Substance for Abstract: Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B. Information

    Substance Name: Bone Morphogenetic Protein Receptors, Ty

    Registry Number: EC 2.7.1.37

    Grant and Affiliation Information for Estimated glomerular filtration rate in sickle cell anemia is associated with polymorphisms of bone morphogenetic protein receptor 1B.

    AFFILIATION: Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NHLBI

    GRANT: T32 HL007501

    ACRONYM: HL

    MEDLINETA: Am J Hematol

    REFSOURCE:

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    ACCESSION NUMBER:

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