Angiotensin converting enzyme gene polymorphism in Korean patients with primary knee osteoarthritis

被引:32
作者
Hong, SJ
Yang, HI
Yoo, MC
In, CS
Yim, SV
Jin, SY
Choe, BK
Chung, JH
机构
[1] Kyung Hee Univ, Coll Med, Dept Internal Med, Div Rheumatol, Seoul 130702, South Korea
[2] Kyung Hee Univ, Coll Med, Dept Orthoped Surg, Seoul 130702, South Korea
[3] Kyung Hee Univ, Coll Oriental Med, Dept Acupuncture, Seoul 130702, South Korea
[4] Kyung Hee Univ, Coll Med, Dept Internal Med, Div Rheumatol, Seoul 130702, South Korea
关键词
angiotensin converting enzyme; osteoarthritis; polymorphism; risk factor;
D O I
10.1038/emm.2003.26
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Angiotensin converting enzyme (ACE) plays an important role in the physiology of vasculature, blood pressure and inflammation. ACE gene, known to have insertion/deletion (I/D) polymorphism, has been widely investigated in its relation with cardiovascular and neurodegenerative diseases and longevity. ACE gene polymorphism in an inflammation associated osteoarthritis (OA) patients is not known. Here we have investigated ACE gene polymorphism in 142 Korean primary knee OA patients and 135 healthy volunteers to establish any clinical correlates between ACE polymorphism and knee osteoarthritis. Clinical parameters such as disease onset age, Kellgren-Lawrence grade and Lequesne's functional index provided additional analysis of the relationship of ACE polymorphism and clinical features of OA. Early onset OA showed significantly higher allele frequency and carriage rate of I than late onset OA. Radiographically severe and functionally poor OA showed higher carriage rate of I allele than radiographically mild and functionally good OA, respectively. This study first reports ACE gene polymorphism to be a risk factor for early onset, severe form primary knee OA.
引用
收藏
页码:189 / 195
页数:7
相关论文
共 29 条
[1]   A deletion in the angiotensin converting enzyme (ACE) gene is common among African Americans with essential hypertension [J].
Asamoah, A ;
Yanamandra, K ;
Thurmon, TF ;
Richter, R ;
Green, R ;
Lakin, T ;
Martin, C .
CLINICA CHIMICA ACTA, 1996, 254 (01) :41-46
[2]   DELETION POLYMORPHISM IN THE GENE FOR ANGIOTENSIN-CONVERTING ENZYME IS A POTENT RISK FACTOR FOR MYOCARDIAL-INFARCTION [J].
CAMBIEN, F ;
POIRIER, O ;
LECERF, L ;
EVANS, A ;
CAMBOU, JP ;
ARVEILER, D ;
LUC, G ;
BARD, JM ;
BARA, L ;
RICARD, S ;
TIRET, L ;
AMOUYEL, P ;
ALHENCGELAS, F ;
SOUBRIER, F .
NATURE, 1992, 359 (6396) :641-644
[3]  
CAMBIEN F, 1988, AM J HUM GENET, V43, P774
[4]   Kallikrein cascade and cytokines in inflamed joints [J].
Cassim, B ;
Mody, G ;
Bhoola, KD .
PHARMACOLOGY & THERAPEUTICS, 2002, 94 (1-2) :1-34
[5]   Immunolocalization of bradykinin receptors on human synovial tissue [J].
Cassim, B ;
Naidoo, S ;
Ramsaroop, R ;
Bhoola, KD .
IMMUNOPHARMACOLOGY, 1997, 36 (2-3) :121-125
[6]   Deletion polymorphism of the angiotensin-converting enzyme gene is independently associated with left ventricular mass and geometric remodeling in systemic hypertension [J].
Gharavi, AG ;
Lipkowitz, MS ;
Diamond, JA ;
Jhang, JS ;
Phillips, RA .
AMERICAN JOURNAL OF CARDIOLOGY, 1996, 77 (15) :1315-1319
[7]   Vascular mechanisms in osteoarthritis [J].
Ghosh, P ;
Cheras, PA .
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2001, 15 (05) :693-709
[8]   ANGIOTENSIN-I CONVERTING-ENZYME (ACE) GENE POLYMORPHISM AND ESSENTIAL-HYPERTENSION IN JAPAN - ETHNIC DIFFERENCE OF ACE GENOTYPE [J].
ISHIGAMI, T ;
IWAMOTO, T ;
TAMURA, K ;
YAMAGUCHI, S ;
IWASAWA, K ;
UCHINO, K ;
UMEMURA, S ;
ISHII, M .
AMERICAN JOURNAL OF HYPERTENSION, 1995, 8 (01) :95-97
[9]   Angiotensin I converting enzyme gene polymorphism in Chinese patients with hypertension [J].
Jeng, JR ;
Harn, HJ ;
Jeng, CY ;
Yueh, KC ;
Shieh, SM .
AMERICAN JOURNAL OF HYPERTENSION, 1997, 10 (05) :558-561
[10]   Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease [J].
Kehoe, PG ;
Russ, C ;
McIlroy, S ;
Williams, H ;
Holmans, P ;
Holmes, C ;
Liolitsa, D ;
Vahidassr, D ;
Powell, J ;
McGleenon, B ;
Liddell, M ;
Plomin, R ;
Dynan, K ;
Williams, N ;
Neal, J ;
Cairns, NJ ;
Wilcock, G ;
Passmore, P ;
Lovestone, S ;
Williams, J ;
Owen, MJ .
NATURE GENETICS, 1999, 21 (01) :71-72