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. 2013:2013:742545.
doi: 10.1155/2013/742545. Epub 2013 Feb 28.

Environmental lead exposure accelerates progressive diabetic nephropathy in type II diabetic patients

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Environmental lead exposure accelerates progressive diabetic nephropathy in type II diabetic patients

Wen-Hung Huang et al. Biomed Res Int. 2013.

Abstract

Whether environmental lead exposure has a long-term effect on progressive diabetic nephropathy in type II diabetic patients remains unclear. A total of 107 type II diabetic patients with stage 3 diabetic nephropathy (estimated glomerular filtration rate (eGFR) range, 30-60 mL/min/1.73 m(2)) with normal body lead burden (BLB) (<600 μ g/72 hr in EDTA mobilization tests) and no history of exposure to lead were prospectively followed for 2 years. Patients were divided into high-normal BLB (>80 μ g) and low-normal BLB (<80 μ g) groups. The primary outcome was a 2-fold increase in the initial creatinine levels, long-term dialysis, or death. The secondary outcome was a change in eGFR over time. Forty-five patients reached the primary outcome within 2 years. Although there were no differences in baseline data and renal function, progressive nephropathy was slower in the low-normal BLB group than that in the high-normal BLB group. During the study period, we demonstrated that each 100 μ g increment in BLB and each 10 μ g increment in blood lead levels could decrease GFR by 2.2 mL/min/1.72 m(2) and 3.0 mL/min/1.72 m(2) (P = 0.005), respectively, as estimated by generalized equations. Moreover, BLB was associated with increased risk of achieving primary outcome. Environmental exposure to lead may have a long-term effect on progressive diabetic nephropathy in type II diabetic patients.

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Figures

Figure 1
Figure 1
Flow chart showing the enrollment and status of patients.
Figure 2
Figure 2
Kaplan-Meier analysis showing that patients with high body lead burden (BLB) (>80 and <600 μg) had a higher likelihood (58.1%, 36/62) of achieving the primary endpoint than those with low BLB (<80 μg) (33.3%, 9/27; Logrank tests, Chi-square = 5.17,  P = 0.023) during the 24-month followup period.

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