Serviços Personalizados
Journal
Artigo
Indicadores
- Citado por SciELO
- Acessos
Links relacionados
- Similares em SciELO
Compartilhar
Portuguese Journal of Nephrology & Hypertension
versão impressa ISSN 0872-0169
Port J Nephrol Hypert vol.29 no.1 Lisboa mar. 2015
EDITORIAL
CKD in disadvantaged populations
Guillermo Garcia-Garcia1, Vivekanand Jha2
on behalf of the World Kidney Day Steering Committee*
1 Nephrology Service, Hospital Civil de Guadalajara University of Guadalajara Health Sciences Center Guadalajara, Jal. Mexico
2 Postgraduate Institute of Medical Education and Research, Chandigarh, India, George Institute for Global Health, New Delhi, India and University of Oxford, United Kingdom
March 12, 2015 will mark the 10th anniversary of World Kidney Day (WKD), an initiative of the International Society of Nephrology and the International Federation of Kidney Foundations. Since its inception in 2006, WKD has become the most successful effort ever mounted to raise awareness among decision-makers and the general public about the importance of kidney disease. Each year WKD reminds us that kidney disease is common, harmful and treatable. The focus of WKD 2015 is on CKD in Disadvantaged Populations. This article reviews the key links between poverty and CKD and the consequent implications for the prevention of kidney disease and the care of kidney patients in these populations.
Chronic kidney disease (CKD) is increasingly recognized as a global public health problem and a key determinant of the poor health outcomes. There is compelling evidence that disadvantaged communities, i.e., those from low resource, racial and minority ethnic communities and/or indigenous and socially disadvantaged backgrounds, suffer from marked increases in the burden of unrecognized and untreated CKD. Although the entire populations of some low and middle-income countries could be considered disadvantaged, further discrimination on the basis of local factors creates a position of extreme disadvantage for certain population groups (peasants, those living in some rural areas, women, the elderly, religious minorities, etc). The fact that even in developed countries, racial and ethnic minorities bear a disproportionate burden of CKD and have worse outcomes, suggests there is much to learn beyond the traditional risk factors contributing to CKD-associated complications1.
About 1.2 billion people live in extreme poverty worldwide. Poverty negatively influences healthy behaviors, health care access and environmental exposure, all of which contribute to health care disparities2 (Table 1). The poor are more susceptible to disease because of lack of access to goods and services, in particular clean water and sanitation, information about preventive behaviors, adequate nutrition, and reduced access to healthcare3.
CKD IN DEVELOPED COUNTRIES
In the US, ethnic minorities have a higher incidence of end-stage renal disease (ESRD). Despite similar prevalence rates for early stages of CKD4, poor outcomes such as ESRD are 1.5-4 times higher2,5-7 among minorities (i.e., African Americans, Hispanics and Native Americans). Poverty further increases the disparity in ESRD rates, with African-Americans being at greater risk8. In the UK, rates of treated ESRD are higher in ethnic minority groups and with increasing social deprivation9. Similarly in Singapore, the CKD prevalence is higher among Malays and Indians compared to the Chinese, with socioeconomic and behavioral factors accounting for 70-80% of the excess risk10.
The incidence of ESRD is also higher among the less advantaged indigenous populations in developed countries. Canadian First Nations people experience ESRD at rates 2.5-4 times higher than the general population11. In Australia, the increase in the number of indigenous people starting renal replacement threapy (RRT) over the past 25 years exceeded that of the non-indigenous population by 3.5 fold, largely due to a disproportionate (> 10-fold) difference in ESRD due to type II diabetic nephropathy, a disease largely attributable to lifestyle issues such as poor nutrition and lack of exercise12. Indigenous populations also have a higher incidence of ESRD due to glomerulonephritis and hypertension13. Compared to the US general population, the ESRD incidence rate is higher in Guam and Hawaii, where the proportion of indigenous people is high, again driven primarily by diabetic ESRD14. Native Americans have a greater prevalence of albuminuria and higher ESRD incidence rate15-18. Nearly three-quarters of all incident ESRD cases among this population have been attributable to type II diabetes.
CKD IN DEVELOPING COUNTRIES
Poverty related factors, such as infectious diseases secondary to poor sanitation, inadequate supply of safe water, environmental pollutants and high concentrations of disease-transmitting vectors continue to play an important role in the development of CKD in low-income countries. Although rates of diabetic nephropathy are rising, chronic glomerulonephritis and interstitial nephritis are among the principal causes of CKD in many countries. Of note is the emergence of HIV-associated nephropathy as the major cause of CKD in Sub-Saharan Africa19.
A high prevalence of CKD of unknown etiology has been reported in rural agricultural communities from Central America, Egypt, India and Sri Lanka.
Male farmworkers are affected disproportionately, and the clinical presentation is suggestive of interstitial nephritis, confirmed on renal biopsies. The strong association with farm work has led to suggestions that exposure to agrochemicals, dehydration, and consumption of contaminated water might be responsible20. Additionally, the use of traditional herbal medications is common and frequently associated with CKD among the poor21,22. In Mexico, CKD prevalence among the poor is 2-3 fold higher than the general population, and the etiology is unknown in 30% of ESRD patients23-26.
LOW-BIRTH WEIGHT AND RISK OF CKD IN THE DISADVANTAGED
POPULATIONS
An association between low birth weight (LBW) due primarily to nutritional factors and kidney disease has been described in disadvantaged populations.
The frequency of LBW is more than double in the Aboriginal pupulation than in the non-Aboriginal population of Australia. The high prevalence of albuminuria in this population has been linked to low nephron number related to low birth weight27,28.
Morphometric studies of kidney biopsies in the Aboriginals show glomerulomegaly, perhaps secondary to nephron deficiency, which might predispose to glomerulosclerosis29,30. A correlation between LBW and CKD has also been described in poor African Americans and Caucasians living in the Southeastern US31. Similarly, in an Indian cohort, low birth weight and early malnutrition were associated with later development of metabolic syndrome, diabetes and diabetic nephropathy32. The finding of a high prevalence of proteinuria, elevated blood pressure and CKD of unknown etiology in South Asian children may also be explained by this mechanism33,34.
DISPARITIES IN ACCESS TO RENAL
REPLACEMENT THERAPY
A recent analysis shows that, globally, there were 2.6 million people on dialysis in 2010, 93% in high or upper middle-income countries. By contrast, the number of people requiring RRT was estimated at 4.9-9 million, suggesting that at least 2.3 million died prematurely because of lack of access to RRT.
Even though diabetes and hypertension increase the burden of CKD, the current provision of RRT is linked largely to two factors: per capita GNP and age, suggesting that poverty is a major disadvantage for receiving RRT. By 2030, the number of people receiving RRT around the world is projected to increase to 5.4 million. Most of this increase will be in developing countries of Asia and Africa35.
Access to RRT in the emerging world is dependent mostly on the health care expenditures and economic strength of individual countries, with the relationship between income and access to RRT being almost linear in low and middle-income countries19,36. In Latin America, RRT prevalence and kidney transplantation rates correlate significantly with gross national income and health expenditure37, while in India and Pakistan, less than 10% of all ESRD patients have access to RRT38. Additionally, developing countries have low transplant rates because of a combination of low levels of infrastructure; geographical remoteness; lack of legislation governing brain death; religious, cultural and social constraints; and commercial incentives that favour dialysis39.
There are also differences in utilization of renal replacement modalities between indigenous and nonindigenous groups in the developed countries. In Australia and New Zealand, the proportion of people receiving home dialysis is considerably lower among indigenous people. At the end of 2007 in Australia, 33% of non-indigenous people requiring RRT were receiving home-based dialysis therapies, in contrast to 18% of Aboriginal people. In New Zealand, homebased dialysis was utilized by 62% of non-indigenous RRT population but only by 42% of Maori/Pacific Islanders12.
The rate of kidney transplantation is also lower amongst disadvantaged communities. Maori and Pacific people are only 25% as likely to get a transplant as European New Zealanders, and the proportion of indigenous people who underwent transplantation and had a functioning kidney transplant is lower among Aboriginal Australians (12%) compared to non-indigenous Australians (45%). In the UK, white individuals from socially deprived áreas, South Asians and blacks were all less likely to receive a pre-emptive renal transplant or living donor transplants than their more affluent white counterparts9. A multinational study found that when compared with white patients, the likelihood of receiving a transplant for Aboriginal patients was 77% lower in Australia and New Zealand, and 66% lower in Canadian First Nations individuals40.
Disparities in renal care are more evident in developing nations. Data from India show that there are fewer nephrologists and nephrology services in the poorer states. As a result, people living in these states are likely to receive less care41. In Mexico, the fragmentation of the health care system has resulted in unequal access to renal replacement therapy. In the state of Jalisco, the acceptance and prevalence rates in the more economically advantaged insured population were higher (327 pmp and 939 pmp, respectively) than for patients without medical insurance (99 pmp and 166 pmp, respectively) The transplant rate also was dramatically different, at 72 pmp for those with health insurance and 7.5 pmp for those without it42.
THE BIDIRECTIONAL RELATIONSHIP BETWEEN POVERTY AND CKD
In addition to having a higher disease burden, the poor have limited access to resources for meeting the treatment costs. A large proportion of patients who are forced to meet the expensive ESRD treatment costs by incurring out-of-pocket expenditure, get pushed into extreme poverty. In one Indian study, over 70% patients undergoing kidney transplantation experienced catastrophic healthcare expenditures43.
Entire families felt the impact of this, including job losses and interruptions in education of children.
OUTCOMES
Overall mortality rates among those who do receive RRT are higher in the indigenous, minorities, and the uninsured populations, even after adjustment for comorbidities.
The hazard ratios for death on dialysis relative to the non-indigenous group are 1.4 for Aboriginal Australians and New Zealand Maori44. The Canadian First Nations patients achieve target levels for BP and mineral metabolism less frequently45. Inthe US, living in predominantly black neighborhoods was associated with higher than expected mortality rates on dialysis and increased time to transplantation46.
Similarly, black patients on PD had a higher risk of death or technique failure compared to whites47.
In Mexico, the mortality on PD is three-fold higher among the unisured population compared to Mexican patients receiving treatment in the US, and the survival rate is significantly lower than the insured Mexican population48, while in India almost two-thirds of the patients are unable to continue dialysis beyond the first 3 months due to financial reasons49.
SUMMARY
The increased burden of CKD in disadavantaged populations is due to both global factors and population-specific issues. Low socioeconomic status and poor access to care contribute to health care disparities, and exacerbate the negative effects of genetic or biologic predisposition. Provision of appropriate renal care to these populations requires a two-pronged approach: expanding the reach of dialysis through development of low-cost alternatives that can be practised in remote locations, and implementation and evaluation of cost-effective prevention strategies. Kidney transplantation should be promoted by expanding deceased donor transplant programs and use of inexpensive, generic immunosuppressive drugs. The message of WKD 2015 is that a concerted attack against the diseases that lead to ESRD, by increasing community outreach, better education, improved economic opportunity, and access to preventive medicine for those at highest risk, could end the unacceptable relationship between CKD and disadvantage in these communities.
References
1. Pugsley D, Norris KC, Garcia-Garcia G, Agodoa L. Global approaches for understanding the disproportionate burden of chronic kidney disease. Ethn Dis 2009;19(Suppl 1): S1-1S1-2. [ Links ]
2. Crews DC, Charles RF, Evans MK, Zonderman AB, Powe NR. Poverty, race, and CKD in a racially and socioeconomically diverse urban population. Am J Kidney Dis 2010: 55(6):992-1000. [ Links ]
3. Sachs JD. Macroeconomics and health: Investing in health for economic development. Report of the Commission on Macroeconomics and Health. WHO. 2001. [ Links ]
4. Kalantar-Zadhe K, Block G, Humphreys MH, Kopple JD. Reverse epidemiology of cardiovascular risk factors in maintenance dialysis patients. Kidney Int 2003;63(3):793-808. [ Links ]
5. Hsu CY, Lin F, Vittinghof E, Shlipak MG. Racial differences in the progression from chronic renal insufficiency to end-stage renal disease in the United States. J Am Soc Nephrol 2003;14(11): 29022907. [ Links ]
6. Norris K, Nissenson AR. Race, gender, and socioeconomic disparities in CKD in the United States. J Am Soc Nephrol 2008;19(7):12611270. [ Links ]
7. Bruce MA, Beech BM, Crook ED, et al. Association of socioeconomic status and CKD among African Americans: The Jackson Heart Study. Am J Kidney Dis 2010;55(6):1001-1008. [ Links ]
8. Volkova N, McClellan W, Klein M, et al. Neighborhood poverty and racial differences in ESRD incidence. J Am Soc Nephrol. 2008;19(2):356-64. [ Links ]
9. Caskey FJ. Renal replacement therapy: can we separate the effects of social deprivation and ethnicity? Kidney Int Suppl 2013;3(2):246249. [ Links ]
10. Sabanayagam C, Lim SC, Wong TY, Lee J, Shankar A, Tai ES. Ethnic disparities in prevalence and impact of risk factors of chronic kidney disease. Nephrol Dial Transplant 2010;25(8):25642570. [ Links ]
11. Gao S, Manns BJ, Culleton BF, et al. Prevalence of chronic kidney disease and survival among aboriginal people. J Am Soc Nephrol 2007;18(11): 2953-2959. [ Links ]
12. McDonald S. Incidence and treatment of ESRD among indigenous peoples of Australasia. Clin Nephrol 2010;74(Suppl 1): S28-S31. [ Links ]
13. Collins JF. Kidney disease in Maori and Pacific people in New Zealand. Clin Nephrol 2010; 74(Suppl 1):S61-S65. [ Links ]
14. Weil EJ, Nelson RG. Kidney disease among the indigenous peoples of Oceania. Ethn Dis 2006;16(Suppl 2):S24-S30. [ Links ]
15. United States Renal Data System: USRDS 2006 Annual Data Report. National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, 2013. [ Links ]
16. Kasiske BL, Rith-Najarian S, Casper ML, Croft JB. American Indian heritage and risk factors for renal injury. Kidney Int 1998;54(4):13051310. [ Links ]
17. Nelson RG, Morgenstern H, Bennett PH. An epidemic of proteinuria in Pima Indians with type 2 diabetes mellitus. Kidney Int 1998;54(6):20812088. [ Links ]
18. Scavini M, Shah VO, Stidley CA, et al. Kidney disease among the Zuni Indians: The Zuni Kidney Project. Kidney Int Suppl 2005;97:S126-S131. [ Links ]
19. Jha V, Garcia-Garcia G, Iseki K, et al. Chronic kidney disease: global dimension and perspectives. Lancet 2013;382(9888):260-272. [ Links ]
20. Almaguer M, Herrera R, Orantes CM. Chronic kidney disease of unknown etiology in agricultural communities. MEDICC Rev 2014;16(2):9-15 [ Links ]
21. Ulasi II, Ijoma CK, Onodugo OD, et al. Towards prevention of chronic kidney disease in Nigeria; a community-based study in Southeast Nigeria. Kidney Int Suppl 2013;3:195-201. [ Links ]
22. Otieno LS, McLigeyo SO, Luta M. Acute renal failure following the use of herbal medicines. East Afr Med J 1991;68(12):993-998. [ Links ]
23. Obrador GT, Garcia-Garcia G, Villa AR, et al. Prevalence of chronic kidney disease in the Kidney Early Evaluation Program (KEEP) Mexico and comparison with KEEP US. Kidney Int 2010; 77Suppl 116:S2-S8. [ Links ]
24. Gutierrez-Padilla JA, Mendoza-Garcia M, Plascencia-Perez S, et al. Screening for CKD and cardiovascular disease risk factors using mobile clinics in Jalisco, Mexico. Am J Kidney Dis 2010; 55(3):474-484. [ Links ]
25. Garcia-Garcia G, Gutierrez-Padilla AJ, Chavez-Iñiguez J, et al. Identifying undetected cases of chronic kidney disease in Mexico.> Targeting high-risk populations. Arch Med Res 2013;44(8):623-627. [ Links ]
26. Amato D, Alvarez-Aguilar C, Castañeda-Limones R, et al. Prevalence of chronic kidney disease in an urban Mexican population. Kidney Int Suppl 2005;97:S11-S17. [ Links ]
27. Hoy W, McDonald SP. Albuminuria: Marker or target in indigenous populations. Kidney Int Suppl 2004;66 92:S25-S31. [ Links ]
28. McDonald SP, Maguire GP, Hoy WE. Renal function and cardiovascular risk markers in a remote Australian Aboriginal community. Nephrol Dial Transplant 2003;18(8):15551561. [ Links ]
29. Hoy WE, Samuel T, Mott SA, et al. Renal biopsy findings among Indigenous Australians: a nationwide review. Kidney Int 2012;82(12):13211331. [ Links ]
30. Hoy WE, Hughson MD, Zimanyi M, et al. Distribution of volumes of individual glomeruli in kidneys at autopsy: association with age, nephron number, birthweight and body mass index. Clin Nephrol 2010;74 Suppl 1: S105S112. [ Links ]
31. Lackland DT, Bendall HE, Osmond C, Egan BM, Barker DJ. Low birth weights contribute to high-rates of early-onset of chronic renal failure in the Southeastern United States. Arch Intern Med 2000;160(10):1472-1476. [ Links ]
32. Bhargava SK, Sachdev HS, Fall CH, et al. Relation of serial changes in childhood body-mass index to impaired glucose tolerance in young adulthood. N Engl J Med 2004; 350(9):865875. [ Links ]
33. Jafar TH, Chaturvedi N, Hatcher J, et al. Proteinuria in South Asian children: prevalence and determinants. Pediatr Nephrol 2005; 20(10):14581465. [ Links ]
34. Jafar TH, Islam M, Poulter N, et al. Children in South Asia have higher body massadjusted blood pressure levels than white children in the United States: a comparative study. Circulation 2005; 111(10):12911297. [ Links ]
35. Liyanage T, Ninomiya T, Jha V, Patrice HM, Okpechi I, Zhao M, Lv J, Garg AX, Knight J, Gallagher M, Kotwal S, Cass A, Perkovic V. Worldwide access to treatment for end stage kidney disease: a systematic review (in press in the Lancet). [ Links ]
36. Barsoum R.S. Chronic kidney disease in the developing world. N Engl J Med 2006; 354(10):997-999. [ Links ]
37. Cusumano AM, Garcia-Garcia G, Gonzalez-Bedat MC, et al. Latin American Dialysis and Transplant Registry: 2008 prevalence and incidence of end-stage renal disease and correlation with socioeconomic indexes. Kidney Int Suppl 2013;3:153156. [ Links ]
38. Jha V. Current status of end-stage renal disease care in India and Pakistan. Kidney Int Suppl 2013; 3:157160. [ Links ]
39. Garcia-Garcia G, Harden PN, Chapman J; World Kidney Day Steering Committee 2012. The global role of kidney transplantation. Lancet 2012;379(9820):e36-e38. [ Links ]
40. Yeates KE, Cass A, Sequist TD, et al. Indigenous people in Australia, Canada, New Zealand and the United States are less likely to receive renal transplantation. Kidney Int 2009; 76(6): 659-664. [ Links ]
41. Jha V. Current status of chronic kidney disease care in southeast Asia. Semin Nephrol 2009;29(5):487-496. [ Links ]
42. Garcia-Garcia G, Monteon-Ramos JF, Garcia-Bejarano H, et al. Renal replacement therapy among disadvantaged populations in Mexico: a report from the Jalisco Dialysis and Transplant Registry (REDTJAL). Kidney Int Suppl 2005;68(97):S58-S61. [ Links ]
43. Ramachandran R, Jha V. Kidney transplantation is associated with catastrophic out of pocket expenditure in India. PLoS ONE 2013;8(7):e67812. [ Links ]
44. McDonald SP, Russ GR. Burden of end-stage renal disease among indigenous peoples in Australia and New Zealand. Kidney Int Suppl 2003;63(83):S123S127. [ Links ]
45. Chou SH, Tonelli M, Bradley JS, Gourishankar S, Hemmelgarn BR; Alberta Kidney Disease Network. Quality of care among Aboriginal hemodialysis patients. Clin J Am Soc Nephrol 2006;1(1): 5863. [ Links ]
46. Rodriguez RA, Sen S, Mehta K, Moody-Ayers S, Bacchetti P, OHare AM. Geography matters: Relationships among urban residential segregation, dialysis facilities, and patient outcomes. Ann Intern Med 2007;146(7):493501. [ Links ]
47. Mehrotra R, Story K, Guest S, Fedunyszyn M. Neighborhood location, rurality, geography and outcomes of peritoneal dialysis patients in the United States. Perit Dial Int 2012; 32(3):322331. [ Links ]
48. Garcia-Garcia G, Briseño-Renteria G, Luquin-Arellano VH, Gao Z, Gill J, Tonelli M. Survival among patients with kidney failure in Jalisco. J Am Soc Nephrol 2007;18(6):1922-1927. [ Links ]
49. Parameswaran S, Geda SB, Rathi M, et al. Referral pattern of patients with end-stage renal disease at a public sector hospital and its impact on outcome. Natl Med J India 2011; 24(4):208-213. [ Links ]
Correspondence to:
World Kidney Day, International Society of Nephrology,
Rues de Fabriques 1B,
1000, Brussels, Belgium
E-mail: info@worldkidneyday.org
Conflict of interest statement: None declared.
Received for publication: 14/10/2014
Accepted: 16/10/2014