pubmed-article:11699055 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C0015780 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C0152035 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C0011860 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C0014442 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C0010200 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C0914912 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C1442161 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C1955829 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C1333402 | lld:lifeskim |
pubmed-article:11699055 | lifeskim:mentions | umls-concept:C0678951 | lld:lifeskim |
pubmed-article:11699055 | pubmed:issue | 11 | lld:pubmed |
pubmed-article:11699055 | pubmed:dateCreated | 2001-11-7 | lld:pubmed |
pubmed-article:11699055 | pubmed:abstractText | To investigate the genetic susceptibility associated with cough related to angiotensin-converting enzyme inhibitor (ACEI) therapy in patients with type 2 diabetes, 189 non-insulin-dependent diabetes mellitus (NIDDM) patients with proteinuria or hypertension treated with perindopril were studied. Cough was considered to be present if the patients had been bothered by a cough during treatment and if they had had related symptoms for at least 2 weeks without an identifiable cause. Polymerase chain reaction (PCR) coupled with single-strand conformation polymorphism (SSCP) was used to detect polymorphisms of ACE and bradykinin B2-receptor genes. After 8 weeks of treatment, 49.2% (93 of 189) of our NIDDM patients were found to be suffering from ACEI-related cough. ACEI-related cough was mainly associated with female patients, with 71.7% (76 of 106) of female and only 20.5% (17 of 83) of male patients experiencing cough after ACEI treatment. There was a significant association of ACE II genotype with ACEI-related cough. The genotype frequencies were 58.2% for II, 47.8% for ID, and 16.7% for DD in patients with ACEI-associated cough and 41.8% for II, 52.2% for ID, and 83.3% for DD in subjects without ACEI-associated cough (chi(2) = 10.268; df = 2, P =.006). As female patients made up the majority of the subjects suffering from ACEI-related cough, we further analyzed the association of ACE I/D genotype with ACEI-related cough separately by sex. Male patients with ACEI-related cough were not associated with ACE I/D genotype distribution, while female patients were strongly associated with ACE I/D genotype polymorphism (chi(2) = 16.12; df = 2; P <.001). There was no association between the bradykinin B2 receptor gene -58T/C polymorphism with ACEI-related cough. In conclusion, our results indicate that Chinese diabetic female subjects are susceptible to ACEI-related cough, and this susceptibility may be genetically predetermined. | lld:pubmed |
pubmed-article:11699055 | pubmed:language | eng | lld:pubmed |
pubmed-article:11699055 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11699055 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11699055 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11699055 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11699055 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11699055 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11699055 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11699055 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11699055 | pubmed:month | Nov | lld:pubmed |
pubmed-article:11699055 | pubmed:issn | 0026-0495 | lld:pubmed |
pubmed-article:11699055 | pubmed:author | pubmed-author:TsaiJ CJC | lld:pubmed |
pubmed-article:11699055 | pubmed:author | pubmed-author:LeeY JYJ | lld:pubmed |
pubmed-article:11699055 | pubmed:copyrightInfo | Copyright 2001 by W.B. Saunders Company | lld:pubmed |
pubmed-article:11699055 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11699055 | pubmed:volume | 50 | lld:pubmed |
pubmed-article:11699055 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11699055 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11699055 | pubmed:pagination | 1346-50 | lld:pubmed |
pubmed-article:11699055 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:meshHeading | pubmed-meshheading:11699055... | lld:pubmed |
pubmed-article:11699055 | pubmed:year | 2001 | lld:pubmed |
pubmed-article:11699055 | pubmed:articleTitle | Angiotensin-converting enzyme gene insertion/deletion, not bradykinin B2 receptor -58T/C gene polymorphism, associated with angiotensin-converting enzyme inhibitor-related cough in Chinese female patients with non-insulin-dependent diabetes mellitus. | lld:pubmed |
pubmed-article:11699055 | pubmed:affiliation | Department of Clinical Research, Ping-Tung Christian Hospital, Ping-Tung, Taiwan, Republic of China. | lld:pubmed |
pubmed-article:11699055 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:11699055 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
entrez-gene:1636 | entrezgene:pubmed | pubmed-article:11699055 | lld:entrezgene |
entrez-gene:624 | entrezgene:pubmed | pubmed-article:11699055 | lld:entrezgene |
entrez-gene:25245 | entrezgene:pubmed | pubmed-article:11699055 | lld:entrezgene |
http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:11699055 | lld:entrezgene |
http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:11699055 | lld:entrezgene |
http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:11699055 | lld:pubmed |