Risk of ESRD in the United States

被引:61
作者
Albertus, Patrick [1 ,2 ]
Morgenstern, Hal [2 ,3 ,4 ,5 ]
Robinson, Bruce [5 ,6 ,7 ]
Saran, Rajiv [1 ,2 ,5 ,7 ]
机构
[1] Univ Michigan, Sch Publ Hlth, Kidney Epidemiol & Cost Ctr, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Publ Hlth, Dept Epidemiol, 1415 Washington Hts, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Publ Hlth, Dept Environm Hlth Sci, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI USA
[5] Univ Michigan, Inst Healthcare Policy & Innovat, Ann Arbor, MI 48109 USA
[6] Univ Michigan, Arbor Res Collaborat Hlth, Ann Arbor, MI 48109 USA
[7] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI USA
关键词
End-stage renal disease (ESRD); incidence; risk; cumulative incidence; risk estimate; lifetime risk; lifetable; racial disparity; US Renal Data System (USRDS); epidemiology; public health; mortality; nationwide surveillance; health inequity; STAGE RENAL-DISEASE; AGE-CONDITIONAL PROBABILITIES; CHRONIC KIDNEY-DISEASE; LIFETIME RISK; VARIANTS ASSOCIATE; RACIAL DISPARITIES; AFRICAN-AMERICAN; APOL1; VARIANTS; BREAST-CANCER; CKD;
D O I
10.1053/j.ajkd.2016.05.030
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Although incidence rates of end-stage renal disease (ESRD) in the United States are reported routinely by the US Renal Data System (USRDS), risks (probabilities) are not reported. Short-and long-term risk estimates need to be updated and expanded to minority populations, including Native Americans, Asian/Pacific Islanders, and Hispanics. Study Design: Risk estimation from surveillance data in large populations using life-table methods. A competing-risks framework was applied by constructing a hypothetical cohort followed from birth to death. Setting & Participants: Total US population. Incidence and mortality rates of ESRD were obtained from the USRDS; all-cause mortality rates were obtained from CDC WONDER. Predictors: Age, sex, race/ethnicity, and year. Outcomes: 10-year to lifetime risks (cumulative incidence) of ESRD. Results: Among males, lifetime risks of ESRD from birth using 2013 data were 3.1% (95% CI, 3.0%-3.1%) for non-Hispanic whites, 8.0% (95% CI, 7.9%-8.2%) for non-Hispanic blacks, 3.8% (95% CI, 3.4%-4.9%) for non-Hispanic Native Americans, 5.1% (95% CI, 4.8%-5.4%) for non-Hispanic Asians/Pacific Islanders, and 6.2% (95% CI, 6.1%-6.4%) for Hispanics. Among females, lifetime risks were 2.0% (95% CI, 2.0%-2.1%) for non-Hispanic whites, 6.8% (95% CI, 6.7%-6.9%) for non-Hispanic blacks, 3.6% (95% CI, 3.3%-4.2%) for non-Hispanic Native Americans, 3.8% (95% CI, 3.6%-4.0%) for non-Hispanic Asian/Pacific Islanders, and 4.3% (95% CI, 4.2%-4.5%) for Hispanics. Lifetime risk of ESRD from birth increased from 3.5% in 2000 to 4.0% in 2013 in males and decreased from 3.0% to 2.8% in females. Limitations: Standard life-time assumption of fixed age-specific rates over time and possible ESRD misclassification. To be useful in clinical practice, this application will require additional predictors (eg, comorbid conditions and chronic kidney disease stage). Conclusions: ESRD risk in the United States varies more than 2-fold among racial/ethnic groups for both sexes. (C) 2016 by the National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:862 / 872
页数:11
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