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开始接受腹膜透析的非糖尿病中国患者出现新发高血糖。

New-onset hyperglycemia in nondiabetic chinese patients started on peritoneal dialysis.

作者信息

Szeto Cheuk-Chun, Chow Kai-Ming, Kwan Bonnie Ching-Ha, Chung Kwok-Yi, Leung Chi-Bon, Li Philip Kam-Tao

机构信息

Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Shatin, Hong Kong, China.

出版信息

Am J Kidney Dis. 2007 Apr;49(4):524-32. doi: 10.1053/j.ajkd.2007.01.018.

Abstract

BACKGROUND

Glucose has been used as the osmotic agent added to standard peritoneal dialysis (PD) solutions since its inception. Patients who have no history of glucose intolerance may develop hyperglycemia after the initiation of PD therapy. However, the prevalence and long-term implications of new-onset hyperglycemia in PD patients has not been studied.

METHODS

We studied 405 consecutive patients with renal failure newly started on PD therapy. Fasting plasma glucose levels 1 month after being stable on PD therapy were reviewed. Clinical factors affecting fasting plasma glucose levels were explored. Patients were followed up for 49.7 +/- 28.4 months.

RESULTS

Of 405 patients, 136 had underlying diabetic nephropathy and another 17 had preexisting diabetes before starting PD therapy. Of the remaining 252 patients, fasting plasma glucose levels were greater than 200 mg/dL (>11.1 mmol/L) in 21 (8.3%) and 126 to 200 mg/dL (7.0 to 11.1 mmol/L) in 48 patients (19.0%). Seven patients required insulin therapy, 3 required low-dose sulfonylurea therapy, and all other patients had glucose levels controlled by means of dietary restriction only. Fasting plasma glucose levels significantly correlated with patient age (Pearson r = 0.278; P < 0.001), Charlson comorbidity score (r = 0.484; P < 0.001), baseline serum C-reactive protein level (r = 0.390; P < 0.001), and serum albumin level (r = -0.182; P < 0.001). However, patients with new-onset hyperglycemia had similar values for body weight, body mass index, peritoneal transport parameters, and ultrafiltration profile compared with other patients. At 36 months, actuarial survival rates were 93.7%, 85.3%, 81.6%, and 66.7% for patients with fasting glucose levels less than 100, 100 to less than 126, 126 to less than 200, and 200 mg/dL or greater (5.6, 5.6 to <7.0, 7.0 to <11.1, and >or=11.1 mmol/L) and 65.9% for patients with preexisting diabetes, respectively (overall log rank test, P < 0.001).

CONCLUSION

New-onset hyperglycemia is common in patients without diabetes started on PD therapy. Contrary to common belief, obese patients do not appear to have a greater risk of hyperglycemia. Our results suggest that even mild hyperglycemia, with fasting plasma glucose level greater than 100 mg/dL (>5.6 mmol/L), is associated with worse survival in PD patients.

摘要

背景

自标准腹膜透析(PD)溶液问世以来,葡萄糖一直被用作渗透剂添加其中。既往无葡萄糖不耐受病史的患者在开始PD治疗后可能会出现高血糖。然而,PD患者新发高血糖的患病率及其长期影响尚未得到研究。

方法

我们研究了405例新开始接受PD治疗的连续性肾衰竭患者。回顾了患者在PD治疗稳定1个月后的空腹血糖水平。探讨了影响空腹血糖水平的临床因素。对患者进行了49.7±28.4个月的随访。

结果

405例患者中,136例有潜在的糖尿病肾病,另外17例在开始PD治疗前已有糖尿病。在其余252例患者中,21例(8.3%)的空腹血糖水平大于200mg/dL(>11.1mmol/L),48例(19.0%)的空腹血糖水平为126至200mg/dL(7.0至11.1mmol/L)。7例患者需要胰岛素治疗,3例需要低剂量磺脲类药物治疗,所有其他患者仅通过饮食限制来控制血糖水平。空腹血糖水平与患者年龄显著相关(Pearson r=0.278;P<0.001)、Charlson合并症评分(r=0.484;P<0.001)、基线血清C反应蛋白水平(r=0.390;P<0.001)和血清白蛋白水平(r=-0.182;P<0.001)。然而,与其他患者相比,新发高血糖患者的体重、体重指数、腹膜转运参数和超滤情况的值相似。在36个月时,空腹血糖水平低于100、100至低于126、126至低于200以及200mg/dL或更高(5.6、5.6至<7.0、7.0至<11.1以及≥11.1mmol/L)的患者的精算生存率分别为93.7%、85.3%、81.6%和66.7%,已有糖尿病的患者的精算生存率为65.9%(总体对数秩检验,P<0.001)。

结论

开始接受PD治疗的非糖尿病患者中,新发高血糖很常见。与普遍看法相反,肥胖患者似乎没有更高的高血糖风险。我们的结果表明,即使是轻度高血糖,空腹血糖水平大于100mg/dL(>5.6mmol/L),也与PD患者较差的生存率相关。

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