Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7311
Title: Angiotensin-converting enzyme gene polymorphism is associated with anemia in non-small-cell lung cancer
Authors: Yaren, A.
Oztop, I.
Turgut, S.
Turgut, G.
Değirmencioğlu, Serkan
Demirpence, M.
Keywords: Anemia
Angiotensin-converting enzyme gene polymorphism
Non-small-cell lung cancer
adult
age distribution
allele
anemia
angiotensin converting enzyme gene
article
blood sampling
computer program
controlled study
DNA polymorphism
female
gene
gene deletion
gene insertion
genetic analysis
genetic association
genotype
human
lung non small cell cancer
major clinical study
male
polymerase chain reaction
sex ratio
statistical analysis
Alleles
Carcinoma, Non-Small-Cell Lung
Case-Control Studies
Erythropoietin
Female
Genetic Predisposition to Disease
Genotype
Humans
Lung Neoplasms
Male
Middle Aged
Polymorphism, Genetic
Renin
Abstract: The angiotensin-converting enzyme (ACE) plays an important role not only in the regulation of vascular homeostasis but also in stimulation of hematopoiesis. We aimed to evaluate the association between insertion/deletion (I/D) polymorphism of the ACE gene and anemia at the time of the diagnosis. We enrolled 75 patients with non-small-cell lung cancer (NSCLC) and 85 age- and sex-matched healthy control participants. The I/D polymorphism of ACE was identified by using polymerase chain reaction from peripheral blood samples. Statistical analyses were performed with SPSS for Windows. The distributions of the ACE genotypes and alleles are similar in patients and in healthy participants (P = 0.29 and P = 0.08, respectively). In patients with NSCLC, 34 (45.3%) had anemia; of whom 3 (8.8%) had genotype II, 24 (70.6%) had genotype ID, and 7 (20.6%) had genotype DD (P = 0.001). The patients with the II and ID genotypes had more frequent anemia at the time of the diagnosis (odds ratio = 6.02; P = 0.001). Our findings suggest that I/D polymorphism of the ACE gene may influence the development of anemia in patients with NSCLC. Copyright © 2008 by the Society for Experimental Biology and Medicine.
URI: https://hdl.handle.net/11499/7311
https://doi.org/10.3181/0705-RM-141
ISSN: 1535-3702
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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