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CLINICAL KIDNEY JOURNAL

Clinical Kidney Journal, 2016, vol. 9, no. 3, 454456


doi: 10.1093/ckj/sfw029
Advance Access Publication Date: 24 May 2016
Editorial Comment

EDITORIAL COMMENT

Diabetes mellitus as a cause of end-stage renal disease in Europe:


signs of improvement
Jan A.J.G. van den Brand
Department of Nephrology, Radboud Institute for Health Science, Radboud University Medical Center, Nijmegen,
The Netherlands
Correspondence and offprint requests to: Jan A.J.G. van den Brand; E-mail: jan.vandenbrand@radboudumc.nl

The ERA-EDTA Registry is an international collaboration collecting data on renal replacement therapy (RRT) in Europe and countries bordering the Mediterranean Sea via national and
international registries. The data are used for focused scientic
studies on specic questions and for epidemiological surveillance of the state of RRT in Europe, which is evaluated annually
and presented in the traditional ERA-EDTA Registry Reports. In
this issue of the Clinical Kidney Journal, Kramer et al. [1] provide a
summary of the 2013 ERA-EDTA Registry Annual Report. At present, the ERA-EDTA Registry covers 49 registries in 34 countries.
Almost two-thirds of these registries offer individual patient
data. The summary focused on diabetes mellitus (DM) as a
cause of end-stage renal disease (ESRD) requiring RRT.
Diabetes is an important health concern. The estimated
prevalence rate of diabetes in Europe was 8.5% in 2013 and is projected to increase to 10.3% in 2035 [2] (Figure 1). It is one of the
main underlying causes of death in adults, accounting for 10%
of all deaths in Europe [3]. Furthermore, persons who have diabetes in addition to chronic kidney disease have an 50% higher
risk of ESRD and death than those at a similar level of estimated
glomerular ltration rate [4]. Therefore, it is an important contributor to RRT in Europe. In total, 477 186 persons in Europe
were receiving RRT in 2013. This amounts to an overall prevalence
rate of 738 patients per million population in Europe and the Mediterranean, and 17% of these patients had DM as the primary cause
of kidney disease. The average incidence rate of RRT in 2013 was
122 persons per million population who started RRT in 2013 in
the ERA-EDTA Registry area. About 24% of the incident RRT
cases had DM as the primary cause of their kidney disease. One
immediately notes the marked difference between the proportion
of incident RRT cases due to DM and the proportion of prevalent
RRT patients with DM. The authors report a markedly poorer 5year survival rate on RRT of 50.6% for patients who had DM as

the primary kidney disease when compared with the overall 5year survival rate on RRT of 60.9%. Fortunately, evaluation of
more recent short-term survival sends a more uplifting message:
the overall 2-year survival rate on RRT has improved from 81.4%
between 2004 and 2008 to 82.7% between 2007 and 2011. This
improved survival rate was even more pronounced in patients
who suffered from ESRD requiring RRT due to diabetes: from
77.3% between 2004 and 2008 to 79.4% between 2007 and 2011.
Even more remarkably were the trends in incidence of RRT
due to DM over the past decade. Despite a decreasing incidence
of DM, its prevalence rate has steadily increased over the past
few decades and is projected to increase even further in the
two decades to come [2, 6]. Given the substantial proportion of
patients with DM who develop chronic kidney disease and ultimately ESRD, one would expect the incidence of RRT as a consequence of DM to increase as well. However, Kramer et al. [1]
show that the incidence of RRT has remained stable over the
past 10 years, even trending towards a slight decrease in recent
years (see Figure 3 of their paper). They made a similar observation on data from the United States Renal Data System (USRDS).
These results mean that the prevention of chronic kidney disease
secondary to DM has improved, at least for Western countries.
Still, the incidence of RRT secondary to DM was ve times
higher in the USA compared with Europe, whereas that of RRT
due to other causes of kidney disease was two times higher.
This may indicate that the progression of CKD to ESRD due to
DM is far greater in the USA compared with Europe. One may
speculate about underlying causes, which could include (i) differences in the management of ESRD, (ii) differences in genetic
background, particularly in African Americans and (iii) differences in the prevalence of risk factors for progressive kidney
damage. A study by van de Luijtgaarden et al. [8] indicated that
nephrologists in high RRT incidence countries were more likely

Received: February 17, 2016. Accepted: March 28, 2016


The Author 2016. Published by Oxford University Press on behalf of ERA-EDTA.
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/
licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
For commercial re-use, please contact journals.permissions@oup.com

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Editorial Comment

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diabetic patients seems to be working, thus curbing the expected


increase in ESRD due to DM. However, despite stabilizing DM incidence in recent years [17], the peak in DM prevalence is still to
come as persons with DM live longer than before. Continued effort is needed to address the underlying causes of diabetes and
diabetic nephropathy at a population level. We seem to have
won the rst battle in the ght against ESRD due to diabetes,
but the war is far from over.

Acknowledgements
J.A.J.G.v.d.B. is supported by a grant from the Dutch Kidney Foundation (DKF14OKG07).

Fig. 1. Trends in diabetes prevalence and forecasted prevalence of diabetes in


Europe. The black line represents the observed prevalence of diabetes over

(See related article by Kramer et al. Renal replacement therapy in


Europe: a summary of the 2013 ERA-EDTA Registry Annual Report
with a focus on diabetes mellitus. Clin Kidney J (2016) 9: 457469.)

time. The dotted, grey line is the forecasted prevalence. Data from Shaw et al.
[5], Danaei et al. [6], Whiting et al. [7] and Guariguata et al. [2].

References

to offer RRT for ESRD, even when they expect gains in quality of
life and survival to be modest [8]. Furthermore, the EVEREST
study indicated that the incidence of RRT was higher in high-income countries with a larger proportion of private for-prot dialysis facilities [9]. This may indicate that, in general, physicians in
the USA may be more willing to start RRT in older patients with
more comorbidities than those in Europe. It highlights an important limitation of the ERA-EDTA date in general: it captures only
treated cases of RRT and not cases of ESRD who are treated conservatively or die prior to the initiation of RRT. An analysis of
USRDS data indicates that even in white Americans, the incidence of RRT is markedly higher compared with Europeans [10].
Therefore, differences in genetic background do not fully explain
the differences in RRT risk between Europe and the USA.
Elevated blood pressure is an important culprit in the progression of diabetic nephropathy. Several trials indicate that aggressive treatment of blood pressure in diabetic patients results in
marked improvement in both overall and renal survival. Perhaps
surprisingly, World Health Organization reports indicate that the
prevalence of elevated blood pressure is substantially higher in
Europe than in the USA [11]. Clearly, differences in blood pressure
control do not explain the difference in RRT risk between Europe
and the USA. Moreover, given the comparatively high frequency of
elevated blood pressure in Europe, there may even be room for improvement in the prevention of ESRD.
If blood pressure does not explain the difference in RRT rate
between the USA and Europe, perhaps other underlying causes
of ESRD are more important. Elevated blood pressure may be
the cause, but also a consequence of vascular damage. Obesity,
poor glycaemic control and hyperlipidaemia all contribute
to vascular damage. Experimental evidence also suggests that
low-grade inammationa consequence of adiposity [12, 13],
hyperglycaemia [14] and hyperlipidaemia [15]have a direct
deleterious effect on the kidney as well. These potential underlying causes of vascular and renal damage are more prevalent
in the USA compared with Europe. A formal comparison between
the USA and Europe may shed light on the determinants for the
marked difference in RRT risk between the two regions, which
may highlight possible differences at a population level rather
than the individual patient level [16]. In turn, such data may
help both physicians and public health workers in the USA and
Europe to improve prevention of ESRD secondary to DM.
All in all, the data presented by Kramer et al. [1] give us reason
to be optimistic, and even though there may be some room
for improvement, secondary prevention of kidney damage in

1.

2.

3.

4.

5.

6.

7.

8.

9.

10.
11.

12.

13.

14.

Kramer A, Pippias M, Stel V et al. Renal replacement therapy


in Europe: a summary of the 2013 ERA-EDTA Registry Annual
Report with a focus on diabetes mellitus. Clin Kidney J 2016; 9:
457469
Guariguata L, Whiting DR, Hambleton I et al. Global estimates
of diabetes prevalence for 2013 and projections for 2035.
Diabetes Res Clin Pract 2014; 103: 137149
IDF Diabetes Atlas Group. Update of mortality attributable to
diabetes for the IDF Diabetes Atlas: estimates for the year
2011. Diabetes Res Clin Pract 2013; 100: 277279
Fox CS, Matsushita K, Woodward M et al. Associations of kidney disease measures with mortality and end-stage renal
disease in individuals with and without diabetes: a metaanalysis. Lancet 2012; 380: 16621673
Shaw JE, Sicree RA, Zimmet PZ. Global estimates of the prevalence of diabetes for 2010 and 2030. Diabetes Res Clin Pract
2010; 87: 414
Danaei G, Finucane MM, Lu Y et al. National, regional, and
global trends in fasting plasma glucose and diabetes prevalence since 1980: systematic analysis of health examination
surveys and epidemiological studies with 370 country-years
and 2.7 million participants. Lancet 2011; 378: 3140
Whiting DR, Guariguata L, Weil C et al. IDF diabetes atlas: global estimates of the prevalence of diabetes for 2011 and 2030.
Diabetes Res Clin Pract 2011; 94: 311321
van de Luijtgaarden MW, Noordzij M, van Biesen W et al. Conservative care in Europenephrologists experience with the
decision not to start renal replacement therapy. Nephrol Dial
Transplant 2013; 28: 26042612
Caskey FJ, Kramer A, Elliott RF et al. Global variation in renal
replacement therapy for end-stage renal disease. Nephrol Dial
Transplant 2011; 26: 26042610
Grams ME, Chow EK, Segev DL et al. Lifetime incidence of CKD
stages 3-5 in the United States. Am J Kidney Dis 2013; 62: 245252
World Health Organization. Global Health ObservatoryBlood
Pressure. http://www.who.int/gho/ncd/risk_factors/blood_
pressure_prevalence/en/
Ix JH, Sharma K. Mechanisms linking obesity, chronic kidney
disease, and fatty liver disease: the roles of fetuin-A, adiponectin, and AMPK. J Am Soc Nephrol 2010; 21: 406412
Wisse BE. The inammatory syndrome: the role of adipose
tissue cytokines in metabolic disorders linked to obesity.
J Am Soc Nephrol 2004; 15: 27922800
JeffersonJA,ShanklandSJ,PichlerRH.Proteinuriaindiabetickidney disease: a mechanistic viewpoint. Kidney Int 2008; 74: 2236

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| J.A.J.G. van den Brand

15. Wahba IM, Mak RH. Obesity and obesity-initiated metabolic


syndrome: mechanistic links to chronic kidney disease. Clin
J Am Soc Nephrol 2007; 2: 550562
16. Rose G. Sick individuals and sick populations. Int J Epidemiol
1985; 14: 3238

17. Centers for Disease Control and Prevention. Crude


and Age-Adjusted Rates of Diagnosed Diabetes per 100 Civilian,
Non-Institutionalized Adult Population, United States, 1980
2014. http://www.cdc.gov/diabetes/statistics/prev/national/
gageadult.htm

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