Citation: | Ramanathan Aravind Selvin Kumar, Karuppiah Balakrishnan, Vijayan Murali, Raju Kamaraj, Mani Dhivakar, Chinniah Rathika, Thirunavukkarasu Manikandan, Ravi Padma Malini, Krishnan Jeyaram Illiayaraja, Senguttuvan Prabha. Effect of angiotensin converting enzyme gene I/D polymorphism in South Indian children with nephrotic syndrome[J]. The Journal of Biomedical Research, 2019, 33(3): 201-207. DOI: 10.7555/JBR.32.20150095 |
[1] |
Srivastava T, Simon SD, Alon US. High incidence of focal segmental glomerulosclerosis in nephrotic syndrome of childhood[J]. Pediatr Nephrol, 1999, 13(1): 13-18. doi: 10.1007/s004670050555
|
[2] |
Hogg R, Middleton J, Vehaskari VM. Focal segmental glomerulosclerosis-epidemiology aspects in children and adults[J]. Pediatr Nephrol, 2007, 22(2): 183-186. http://www.wanfangdata.com.cn/details/detail.do?_type=perio&id=5c93caee40c7bac82d06f6c6f1ae1c7e
|
[3] |
Hogg RJ, Portman RJ, Milliner D, et al. Evaluation and management of proteinuria and nephrotic syndrome in children: recommendations from a pediatric nephrology panel established at the National Kidney Foundation conference on proteinuria, albuminuria, risk, assessment, detection, and elimination (PARADE)[J]. Pediatrics, 2000, 105(6): 1242-1249. doi: 10.1542/peds.105.6.1242
|
[4] |
Sharples PM, Poulton J, White RH. Steroid responsive nephrotic syndrome is more common in Asians[J]. Arch Dis Child, 1985, 60(11): 1014-1017. doi: 10.1136/adc.60.11.1014
|
[5] |
McKinney PA, Feltbower RG, Brocklebank JT, et al. Time trends and ethnic patterns of childhood nephrotic syndrome in Yorkshire, UK[J]. Pediatr Nephrol, 2001, 16(12): 1040-1044. doi: 10.1007/s004670100021
|
[6] |
Li RM, Branton MH, Tanawattanacharoen S, et al. Molecular identification of SV40 infection in human subjects and possible association with kidney disease[J]. J Am Soc Nephrol, 2002, 13(9): 2320-2330. doi: 10.1097/01.ASN.0000028249.06596.CF
|
[7] |
Huang HD, Lin FJ, Li XJ, et al. Genetic polymorphisms of the renin-angiotensin-aldosterone system in Chinese patients with end-stage renal disease secondary to IgA nephropathy[J]. Chin Med J (Engl), 2010, 123(22): 3238-3242. http://cn.bing.com/academic/profile?id=3392708438651b3e1b6274a464ebae3a&encoded=0&v=paper_preview&mkt=zh-cn
|
[8] |
Kopkan L, Cervenka L. Renal interactions of renin-angiotensin system, nitric oxide and superoxide anion: implications in the pathophysiology of salt-sensitivity and hypertension[J]. Physiol Res, 2009, 58(S2): S55-S67. http://cn.bing.com/academic/profile?id=212ba9294f3530c4ea1a42dfd3f5f407&encoded=0&v=paper_preview&mkt=zh-cn
|
[9] |
Parsa A, Peden E, Lum RF, et al. Association of angiotensinconverting enzyme polymorphisms with systemic lupus erythematosus and nephritis: analysis of 644 SLE families[J]. Genes Immun, 2002, 3(S1): S42-S46. doi: 10.1038/sj.gene.6363907
|
[10] |
Uemura K, Nakura J, Kohara K, et al. Association of ACE I/D polymorphism with cardiovascular risk factors[J]. Hum Genet, 2000, 107(3): 239-242. doi: 10.1007/s004390000358
|
[11] |
Lin C, Yang HY, Wu CC, et al. Angiotensin converting enzyme insertion/deletion polymorphism contributes high risk for chronic kidney disease in Asian male with hypertension-a meta-regression analysis of 98 observational studies[J]. PLoS One, 2014, 9(1): e87604. doi: 10.1371/journal.pone.0087604
|
[12] |
Naresh VV, Reddy AL, Sivaramakrishna G, et al. Angiotensin converting enzyme gene polymorphism in type Ⅱ diabetics with nephropathy[J]. Indian J Nephrol, 2009, 19(4): 145-148. doi: 10.4103/0971-4065.59335
|
[13] |
Takezako T, Zhang B, Serikawa T, et al. The D allele of the angiotensin-converting enzyme gene and reperfusion-induced ventricular arrhythmias in patients with acute myocardial infarction[J]. Jpn Circ J, 2001, 65(7): 603-609. doi: 10.1253/jcj.65.603
|
[14] |
Taniguchi I, Yamazaki T, Wagatsuma K, et al. The DD genotype of angiotensin converting enzyme polymorphism is a risk factor for coronary artery disease and coronary stent restenosis in Japanese patients[J]. Jpn Circ J, 2001, 65(10): 897-900. doi: 10.1253/jcj.65.897
|
[15] |
Prasun P, Prasad N, Tripathi G, et al. Association of angiotensin-converting enzyme gene I/D polymorphism with steroid responsiveness in childhood nephrotic syndrome[J]. Indian J Nephrol, 2011, 21(1): 26-29. doi: 10.4103/0971-4065.75215
|
[16] |
Oktem F, Sirin A, Bilge I, et al. ACE I/D gene polymorphism in primary FSGS and steroid-sensitive nephrotic syndrome[J]. Pediatr Nephrol, 2004, 19(4): 384-389. doi: 10.1007/s00467-003-1398-4
|
[17] |
Patil SJ, Gulati S, Khan F, et al. Angiotensin converting enzyme gene polymorphism in Indian children with steroid sensitive nephrotic syndrome[J]. Indian J Med Sci, 2005, 59(10): 431-435. doi: 10.4103/0019-5359.17049
|
[18] |
Jayapalan JJ. Muniandy S, Chan SP. Null association betweenACE gene I/D polymorphism and diabetic nephropathy among multiethnic Malaysian subjects[J]. Indian J Hum Genet, 2008, 16(2): 78-86. http://www.researchgate.net/publication/47622034_Null_association_between_ACE_gene_ID_polymorphism_and_diabetic_nephropathy_among_multiethnic_Malaysian_subjects
|
[19] |
Tsai IJ, Yang YH, Lin YH, et al. Angiotensin-converting enzyme gene polymorphism in children with idiopathic nephrotic syndrome[J]. Am J Nephrol, 2006, 26(2): 157-162. doi: 10.1159/000092982
|
[20] |
Fahmy ME, Fattouh AM, Hegazy RA, et al. ACE gene polymorphism in Egyptian children with idiopathic nephrotic syndrome[J]. Bratisl Lek Listy, 2008, 109(7): 298-301. http://cn.bing.com/academic/profile?id=23df587115d771900b9b52277c517e26&encoded=0&v=paper_preview&mkt=zh-cn
|
[21] |
Al-Eisa A, Haider MZ, Srivastva BS. Angiotensin converting enzyme gene insertion/deletion polymorphism in idiopathic nephrotic syndrome in Kuwaiti Arab children[J]. Scand J Urol Nephrol, 2001, 35(3): 239-242. doi: 10.1080/003655901750292033
|
[22] |
Saber-Ayad M, Sabry S, Abdel-Latif I, et al. Effect of angiotensin-converting enzyme gene insertion/deletion polymorphism on steroid resistance in Egyptian children with idiopathic nephrotic syndrome[J]. J Renin Angiotensin Aldosterone Syst, 2010, 11(2): 111-118. doi: 10.1177/1470320309359021
|
[23] |
Ghorbani A, Omidvar B, Beladi-Mousavi SS, et al. The effect of pentoxifylline on reduction of proteinuria among patients with type 2 diabetes under blockade of angiotensin system: a double blind and randomized clinical trial[J]. Nefrologia, 2012, 32(6): 790-796. http://cn.bing.com/academic/profile?id=a51946f5ff4568562247742b7c288525&encoded=0&v=paper_preview&mkt=zh-cn
|
[24] |
Hohenfellner K, Wingen AM, Nauroth O, et al. Impact of ACE I/D gene polymorphism on congenital renal malformations[J]. Pediatr Nephrol, 2001, 16(4): 356-361. doi: 10.1007/s004670100567
|
[25] |
Sasse B, Hailemariam S, Wüthrich RP, et al. Angiotensin converting enzyme gene polymorphisms do not predict the course of idiopathic nephrotic syndrome in Swiss children[J]. Nephrology (Carlton), 2006, 11(6): 538-541. doi: 10.1111/nep.2006.11.issue-6
|
[26] |
Tabel Y, Berdeli A, Mir S, et al. Effects of genetic polymorphisms of the renin-angiotensin system in children with nephrotic syndrome[J]. J Renin Angiotensin Aldosterone Syst, 2005, 6(3): 138-144. doi: 10.3317/jraas.2005.020
|
[27] |
Celik US, Noyan A, Bayazit AK, et al. ACE gene polymorphism in Turkish children with nephrotic syndrome[J]. Ren Fail, 2006, 28(5): 401-403. doi: 10.1080/08860220600599084
|
[28] |
Shahid S, Abid A, Mehdi SQ, et al. Association of the ACE-Ⅱ genotype with the risk of nephrotic syndrome in Pakistani children[J]. Gene, 2012, 493(1): 165-168. doi: 10.1016/j.gene.2011.10.016
|
[29] |
Serdaroglu E, Mir S, Berdeli A, et al. ACE gene insertion/ deletion polymorphism in childhood idiopathic nephrotic syndrome[J]. Pediatr Nephrol, 2005, 20(12): 1738-1743. doi: 10.1007/s00467-005-2010-x
|
[30] |
Reiser J, von Gersdorff G, Loos M, et al. Induction of B7-1 in podocytes is associated with nephrotic syndrome[J]. J Clin Invest, 2004, 113(10): 1390-1397. doi: 10.1172/JCI20402
|
[31] |
Luther Y, Bantis C, Ivens K, et al. Effects of the genetic polymorphisms of the renin-angiotensin system on focal segmental glomerulosclerosis[J]. Kidney Blood Press Res, 2003, 26(5-6): 333-337. doi: 10.1159/000073939
|
[32] |
Hartleben B, Gödel M, Meyer-Schwesinger C, et al. Autophagy influences glomerular disease susceptibility and maintains podocyte homeostasis in aging mice[J]. J Clin Invest, 2010, 120(4): 1084-1096. doi: 10.1172/JCI39492
|
[33] |
Qiu MY, Xie QF, Wang LN, et al. Association between angiotensin-converting enzyme 2 gene polymorphisms and childhood primary nephrotic syndrome[J]. Zhongguo Dang Dai Er Ke Za Zhi, 2015, 17(3): 232-236. http://d.old.wanfangdata.com.cn/Periodical/zgddekzz201503008
|
[34] |
Sasongko TH, Sadewa AH, Kusuma PA, et al. ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population[J]. Kobe J Med Sci, 2005, 51(3-4): 41-47. http://cn.bing.com/academic/profile?id=d68368d3d12b47570aee3ed8fba7cb9a&encoded=0&v=paper_preview&mkt=zh-cn
|
[35] |
Zhou TB, Qin YH, Su LN, et al. Relationship between angiotensin-converting enzyme insertion/deletion gene polymorphism and susceptibility of minimal change nephrotic syndrome: a meta-analysis[J]. Int J Nephrol, 2011, 2011: 360357. http://cn.bing.com/academic/profile?id=5c0ecadf8603fa0639e2e6214a3f0ebb&encoded=0&v=paper_preview&mkt=zh-cn
|
[36] |
Yuan M, Duan Z, Sun Y, et al. Effects of estrogen on ACE-Ang Ⅱ-AT1 axis in ovariectomy and hypoxic pulmonary hypertension rats[J]. Zhonghua Yi Xue Za Zhi, 2014, 94(22): 1696-1700. http://www.wanfangdata.com.cn/details/detail.do?_type=perio&id=zhyx201422009
|
[37] |
Higaki J, Baba S, Katsuya T, et al. Deletion allele of angiotensin-converting enzyme gene increases risk of essential hypertension in Japanese men: the suita study[J]. Circulation, 2000, 101(17): 2060-2065. doi: 10.1161/01.CIR.101.17.2060
|
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