Chugh K S, Jain S, Sakhuja V, Malik N, Gupta A, Gupta A, Sehgal S, Jha V, Gupta K L
Department of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Q J Med. 1992 Nov-Dec;85(307-308):833-43.
Over a 16-year period, 205 patients with hypertension were shown to have a renovascular aetiology. Of these, 125 (61 per cent) had Takayasu's arteritis, 58 (28.3 per cent) had fibromuscular dysplasia, 16 (7.8 per cent) had atherosclerosis, five (2.4 per cent) had polyarteritis nodosa and one (0.5 per cent) had renal artery aneurysm. Among patients with Takayasu's arteritis, males were affected as commonly as females. The mean age of these patients at the time of detection was 26.8 +/- 8.6 years (range 5-52 years). Type I arteritis was seen in nine (7.2 per cent), Type II in 40 (32 per cent) and Type III in 76 (60.8 per cent) patients. The abdominal aorta was involved in 117 (93.3 per cent) patients. Takayasu's arteritis was associated with ulcerative colitis in two patients and with renal amyloidosis and focal segmental glomerulosclerosis with a nephrotic syndrome in one patient each. Surgical intervention consisting of bypass procedures, autotransplantation or nephrectomy was performed in 17 (13.6 per cent) and angioplasty in nine (7.2 per cent) patients. Cure and improvement in blood pressure was observed in 82.4 per cent and 77.8 per cent respectively. Adequate control of blood pressure was achieved with drugs only in 22 (22.2 per cent) patients. A definite cause and effect relationship could not be established between any infective or immunological disorder and Takayasu's arteritis. Takayasu's arteritis is a far more common cause of renovascular hypertension in Indian population than fibromuscular dysplasia or atherosclerosis, which are more common in the western population.
在16年的时间里,205例高血压患者被证实有肾血管病因。其中,125例(61%)患有高安动脉炎,58例(28.3%)患有纤维肌性发育异常,16例(7.8%)患有动脉粥样硬化,5例(2.4%)患有结节性多动脉炎,1例(0.5%)患有肾动脉动脉瘤。在高安动脉炎患者中,男性和女性受影响的几率相同。这些患者在被发现时的平均年龄为26.8±8.6岁(范围为5至52岁)。9例(7.2%)患者为I型动脉炎,40例(32%)为II型,76例(60.8%)为III型动脉炎。117例(93.3%)患者的腹主动脉受累。2例高安动脉炎患者合并溃疡性结肠炎,各有1例患者合并肾淀粉样变性和局灶节段性肾小球硬化伴肾病综合征。17例(13.6%)患者接受了包括搭桥手术、自体肾移植或肾切除术在内的外科干预,9例(7.2%)患者接受了血管成形术。分别有82.4%和77.8%的患者血压得到治愈和改善。仅通过药物治疗,只有22例(22.2%)患者的血压得到了充分控制。在任何感染性或免疫性疾病与高安动脉炎之间都无法确立明确的因果关系。在印度人群中,高安动脉炎是肾血管性高血压比纤维肌性发育异常或动脉粥样硬化更常见的病因,而纤维肌性发育异常和动脉粥样硬化在西方人群中更常见。