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. 2018 Jul 30;38(8):986-991.
doi: 10.3969/j.issn.1673-4254.2018.08.14.

[Correlation between TGF-B gene promoter-509C/T polymorphism and IgA nephropathy in core families in Guangxi Zhuang Autonomous Region and the therapeutic effect of dendrobium]

[Article in Chinese]
Affiliations

[Correlation between TGF-B gene promoter-509C/T polymorphism and IgA nephropathy in core families in Guangxi Zhuang Autonomous Region and the therapeutic effect of dendrobium]

[Article in Chinese]
Shiliang Li et al. Nan Fang Yi Ke Da Xue Xue Bao. .

Abstract

Objective: To investigate the correlation between transformation growth factor (TGF- B) polymorphisms and IgA nephropathy and the therapeutic effect of dendrobium on IgA nephropathy.

Methods: Polymerase chain reaction- restriction fragment length polymorphism (PCR- RFLP) and direct sequencing were used for analysis of 118 patients with IgA nephropathy from core families in Guangxi Zhuang Autonomous Region. The imbalanced transfer of TGF iso1-509 C/T in the affected offsprings was observed by transfer imbalance test and HRR analysis. The TGF-B genotype of the patients and the core family members were detected. The therapeutic effects of Dendrobium candidum combined with hormone and ACEI/ARB treatments were evaluated by observing the patient's urine protein (24 hUpr), serum albumin (ALB), creatinine (Scr) and urea nitrogen (BUN) levels.

Results: In the 118 patients with IgA nephropathy, we identified TGF-B 1 promoter -509C/T genotype CC in 32 (27.1%) cases, CT in 58 (49.2%) cases, and TT in 28 (23.7%) cases. In the core family of the patients, CC genotype was found in 33 (28.0%) cases, CT in 55 (46.6%) cases, and TT in 30 (28.0%) cases. The treatments significantly lowered 24 hUpr, Scr, and BUN levels (P > 0.05) in patients with CC genotype, significantly lowered 24 hUpr and BUN levels in patients with CT genotype (P < 0.05), and significantly lowered 24 hUpr and BUN level and increased (P < 0.05) ALB level (P < 0.01) in patients with TT genotype.

Conclusions: There is no significant correlation between TGF-B promoter - 509C/T polymorphism and IgA nephropathy. The patients with CC genotype are sensitive to the treatments with hormone and ACEI/ ARB and show a stronger response to combined treatments with dendrobium.

目的: 探讨IgA肾病(IgAN)患者转化生长因子-β(TGF-β)的启动子-509C/T位点多态性及铁皮石斛处方的疗效。

方法: 采用PCR-RFLP和直接测序法鉴定118例桂西壮族IgA肾病患者,按TGF-β1基因测序情况,分为CC、CT和TT三种类型,每种类型随机分为试验组和观察组。另外选取入选患者的兄弟姐妹118例作为家系对照组,采用传递不平衡检验和HRR分析的方法观察TGFβ1-509 C/T在患病子代的不平衡传递。随机抽取具有至少1名健康的兄弟姐妹同胞的壮族IgA N患者,检测患者和核心家系成员的TGF-β基因型,在激素联合ACEI/ARB基础上观察铁皮石斛处方的干预效果,并检测患者尿蛋白定量(24 hUpr)、血清白蛋白(ALB)、肌酐(Scr)、尿素氮(BUN)水平的变化情况。

结果: 桂西壮族IgA N患者TGF-β1启动子-509C/T位点基因CC型32例(占27.1%),CT型58例(占49.2%),TT型28例(占23.7%)。而IgAN患者核心家系人群为CC型33例(占28.4%),CT型55例(占46.6%),TT型30例(占25.0%)。治疗前试验组与观察组差异无统计学意义(P > 0.05),治疗后,CC型:试验组24 hUpr、Scr、BUN水平降低的幅度较观察组高(P < 0.01或P < 0.05)。ALB水平升高的幅度较观察组高,但其差异无统计学意义(P > 0.05);CT型:24 hUpr和BUN水平降低的幅度较观察组高(P < 0.01)。Scr水平降低的幅度较观察组高,ALB水平降低的幅度较观察组高,但其差异无统计学意义(P > 0.05);TT型:24 hUpr、BUN水平降低的幅度较观察组高(P < 0.01或P < 0.05)。ALB水平升高的幅度较观察组高(P < 0.01)。Scr水平降低的幅度较观察组高,但差异无统计学意义(P > 0.05)。

结论: 桂西壮族居民TGF-β启动子-509C/T位点多态性与IgA N患病无关联性;西药联合铁皮石斛处方治疗可有效提高IgA N的临床疗效;携带TGF-β启动子-509基因位点CC型的患者,不仅对西医治疗敏感,对铁皮石斛处方联合干预效果更敏感。

Keywords: Caulis dendrobii; IgA nephropathy; gene polymorphism; transforming growth factor-beta.

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References

    1. Segarra-Medrano A, Carnicer-Caceres C, Valtierra-Carmeno N, et al. Value of urinary levels of interleukin- 6, epidermal growth factor, monocyte chemoattractant protein type1 and transforming growth factor β1 in predicting the extent of fibrosis lesions in kidney biopsies of patients with IgA nephropathy. Nefrologia. 2017;37(5):531–8. doi: 10.1016/j.nefro.2016.11.017. [Segarra-Medrano A, Carnicer-Caceres C, Valtierra-Carmeno N, et al. Value of urinary levels of interleukin- 6, epidermal growth factor, monocyte chemoattractant protein type1 and transforming growth factor β1 in predicting the extent of fibrosis lesions in kidney biopsies of patients with IgA nephropathy[J]. Nefrologia, 2017, 37 (5): 531-8.] - DOI - PubMed
    1. Wang C, Liu X, Peng H, et al. Mesangial cells stimulated by immunoglobin a1 from IgA nephropathy upregulates transforming growth factor-beta 1 synthesis in podocytes via Renin-Angiotensin system activation. Arch Med Res. 2010;41(4):255–60. doi: 10.1016/j.arcmed.2010.05.003. [Wang C, Liu X, Peng H, et al. Mesangial cells stimulated by immunoglobin a1 from IgA nephropathy upregulates transforming growth factor-beta 1 synthesis in podocytes via Renin-Angiotensin system activation[J]. Arch Med Res, 2010, 41(4): 255-60.] - DOI - PubMed
    1. Reeves WB, Andreoli TE. Transforming growth factor beta contributes to progressive diabetic nephropathy. Proc Nati Acad Sci USA. 2000:7667–9. [Reeves WB, Andreoli TE. Transforming growth factor beta contributes to progressive diabetic nephropathy[J]. Proc Nati Acad Sci USA, 2000: 7667-9.] - PMC - PubMed
    1. Luedecking EK, Dekosky ST, Mehdi H, et al. Analysis of genetic polymorphisms in the transforming growth factor-beta1 gene and the risk of Alzheimer's disease. Hum Genet. 2000;106(5):565–9. doi: 10.1007/s004390000313. [Luedecking EK, Dekosky ST, Mehdi H, et al. Analysis of genetic polymorphisms in the transforming growth factor-beta1 gene and the risk of Alzheimer's disease[J]. Hum Genet, 2000, 106(5): 565-9.] - DOI - PubMed
    1. Penfold RS, Prendecki M, Mcadoo S, et al. Primary IgA nephropathy: current challenges and future prospects. Int J Nephrol Renovasc Dis. 2018;11:137–48. doi: 10.2147/IJNRD. [Penfold RS, Prendecki M, Mcadoo S, et al. Primary IgA nephropathy: current challenges and future prospects[J]. Int J Nephrol Renovasc Dis, 2018, 11: 137-48.] - DOI - PMC - PubMed

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