Eren P A, Turan K, Berber I, Canbakan M, Kara M, Tellioglu G, Bugan U, Sevinç C, Turkmen F, Titiz M I
Departments of Molecular Genetics, Haydarpasa Numune Research and Training Hospital, Istanbul, Turkey.
Clin Nephrol. 2009 Aug;72(2):114-21.
The calcium sending receptor (CaSR) allows parathyroid and kidney tubular cells to regulate PTH secretion and tubular calcium reabsorption. In the present report, we examined the relationship between CaSR gene polymorphisms and parathyroid CaSR expression and serum calcium/parathyroid hormone (PTH) levels and clinical progress in ESRD patients in the Turkish population.
We genotyped the CaSR R990G and Q1011E variants in 192 end-stage renal disease (ESRD) patients by allele-specific PCR. CaSR expression in parathyroid tissues of operated 33 patients was quantified with quantitative reverse transcription-PCR.
Compared with other genotypes, the ratio of both codon 990-AA and 1011-CC polymorphisms was found higher in operated patients (p = 0.001). In the total patient group PTH levels were found higher in patients with CC1011 genotype than those with CG1011 (1015.15 +/- 925.41 pg/ml; 523.84 +/- 544.6 pg/ml, respectively, p = 0.002). There were statistically important higher Ca2+ levels in the AA990 allele carrying cases than AG990 positive ones (9.3 +/- 1.0 mg/dl vs. 8.8 +/- 0.9, p = 0.006). On the other hand, the expression of CaSR in parathyroid tissue was found inversely proportional with serum PTH level (r = -0.71).
Present data suggest that co-presence of CaSR gene AA990 and CC1011 alleles is a possible risk factor for bad prognosis in secondary hyperparathyroidism. Patients carrying this genotype have tendency to require operation early in their medical therapy period and need postoperative close follow up for possible recurrences.
钙敏感受体(CaSR)可使甲状旁腺和肾小管细胞调节甲状旁腺激素(PTH)分泌及肾小管钙重吸收。在本报告中,我们研究了土耳其人群中终末期肾病(ESRD)患者的CaSR基因多态性与甲状旁腺CaSR表达、血清钙/甲状旁腺激素(PTH)水平及临床进展之间的关系。
我们采用等位基因特异性PCR对192例终末期肾病(ESRD)患者的CaSR R990G和Q1011E变异进行基因分型。用定量逆转录PCR对33例手术患者甲状旁腺组织中的CaSR表达进行定量分析。
与其他基因型相比,手术患者中密码子990-AA和1011-CC多态性的比例更高(p = 0.001)。在总患者组中,CC1011基因型患者的PTH水平高于CG1011基因型患者(分别为1015.15±925.41 pg/ml;523.84±544.6 pg/ml,p = 0.002)。携带AA990等位基因的病例的Ca2 +水平在统计学上显著高于AG990阳性病例(9.3±1.0 mg/dl对8.8±0.9,p = 0.006)。另一方面,发现甲状旁腺组织中CaSR的表达与血清PTH水平呈负相关(r = -0.71)。
目前的数据表明,CaSR基因AA990和CC1011等位基因的共同存在可能是继发性甲状旁腺功能亢进预后不良的一个风险因素。携带这种基因型的患者在药物治疗期间有较早接受手术的倾向,术后需要密切随访以防复发。