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Environment and chronic kidney disease in farmers

Abstract

The prevalence of chronic kidney disease (CKD) has been on the rise worldwide. Epidemiological studies performed primarily in Central America and South Asia have reported high prevalence of CKD among young and middle-aged men working in agricultural communities. The clinical features do not appear linked to any classical CKD risk factors, such as hypertension, diabetes, or chronic nephritis. The disease develops and progresses as interstitial nephritis, without showing noticeable symptoms or high levels of proteinuria. Pathologically, the disease essentially represents chronic interstitial nephritis and is termed chronic interstitial nephritis in agricultural communities (CINAC). The potential causes of CINAC include: (1) heat stress-related factors associated with increased ambient temperatures resulting from global warming; and (2) factors connected with exposure to agrochemicals and/or pesticides. Global warming and environmental pollution will undoubtedly pose a significant health risk to farmers, and heat stress during farm work could easily result in the development and progression of CKD. Japanese agricultural regions evidently will not be spared from global environmental changes. For future epidemiological studies, researchers should establish a more comprehensive analytical method that can incorporate additional risk-factor variables, such as occupational history (including agricultural work) and ambient temperature.

Introduction

Chronic kidney disease (CKD) is primarily caused by chronic glomerulonephritis, diabetes, or hypertension. In 2017, the global prevalence of CKD was 9.1% [1]. Patients with advanced CKD require renal replacement therapy, significantly impacting their healthcare costs and quality of life. In the past, causes of CKD were often specific renal disorders such as chronic glomerulonephritis and polycystic kidney disease. However, in recent years, an increasing number of patients have initiated maintenance dialysis due to non-specific renal disorders (e.g., diabetic nephropathy and hypertensive nephropathy) associated with aging or lifestyle-related diseases [2]. Moreover, etiologies of CKD cannot even be clarified in a certain number of Japanese patients undergoing chronic dialysis [2].

Recently, environmental and occupational risk factors have drawn global attention as potential causes of CKD, promoting epidemiological studies, pathophysiological assessments, and experimental pathological verification of these risk factors. The results have revealed the prevalence of CKD not only in high-income nations, but also in low- and middle-income countries and regions. In these developing countries and regions, certain individuals without commonly known CKD risk factors (i.e., aging, hypertension, and diabetes) present with kidney injury and progress to end-stage renal failure that requires renal replacement therapy [3].

In this review article, we provide an overview of CKD and its risk factors identified from different agricultural communities around the world. I then describe the current knowledge about the possible mechanisms of kidney injury in farmers.

Epidemiological evidence for hot spots of chronic kidney disease in the agricultural community

Descriptive research into CKD occurring frequently in agricultural workers was initiated in 2002 in Central America [4]. In El Salvador, CKD and end-stage renal failure had been frequently observed among young workers in sugarcane fields since the 1990s, and the number of patients with these kidney diseases had been showing an increasing tendency. These patients did not exhibit any classical risk factors of CKD, such as hypertension, diabetes, or glomerular diseases. A similar phenomenon was also observed in different regions of Central America, including Costa Rica [5] and Nicaragua [6]. These kidney diseases are thus now collectively referred to as Mesoamerican nephropathy (MeN), based on the geographical features of their origins [7]. MeN is also called chronic interstitial nephritis in agricultural communities (CINAC). This is because the disease rarely shows the characteristics of glomerular injury (such as proteinuria), and is defined by its clinical features (primarily renal tubular injury) and pathological hallmarks (chronic interstitial nephritis) [8]. Sugarcane field workers tend to experience repeated episodes of acute kidney injury (AKI) that is caused, for example, by dehydration during work hours [9]. This leads to gradual decreases in renal function over the course of a harvest season, ultimately progressing to CKD. The prevalence of CKD is thus high among sugarcane farmers. In addition to sugarcane work, other types of physical labor (such as cotton farming, corn growing, and construction work) can also cause CINAC [6, 10]. A common feature associated with these occupations is long, physically intensive labor performed by young men in low-altitude farmland [11]. This suggests that the clinical conditions of CINAC patients are caused by a common mechanism involving heat-induced recurrent AKI.

Similar to MeN, CKD not attributable to any classical risk factors has frequently been identified in Sri Lanka since the 1990s [12]. Patients with this kidney disease are predominantly male and between 40 and 50 years old. Cases are initially asymptomatic and the kidney injury progresses with no increase in urinary protein levels. Pathologically, this disease is a chronic interstitial nephritis and its pathophysiology is similar to that of MeN [13, 14]. One difference between MeN and Sri Lankan nephropathy is the working environments, with patients in Central America generally working in sugarcane, cotton, and corn fields, and those in Sri Lanka mainly growing rice in paddy fields [15]. Agricultural workers in Central America and Sri Lanka are thus likely exposed to slightly different types and quantities of water pollutants (i.e., chemical agents and heavy metals) [15].

Hotspots of “CKD with no associated classical risk factors” have been reported in other regions of the world. Kidney diseases in these hotspots as well as MeN and Sri Lankan nephropathy are collectively termed CKD of unknown etiology (CKDu) [3]. In Central India, CKDu is also called “Uddanam nephropathy”, named after a typical village in the state of Andhra Pradesh. In the 1990s, chronic interstitial nephritis found in this Indian region was reported to account for a significant proportion of the clinical features of 2,028 patients with renal failure [16]. Following this first report, a systematic epidemiological study was performed [17]. Hotspots of CKDu have also been identified in Mexico [18], Egypt [19] and others shown in Table 1.

Table 1 Original evidence of kidney disease in agricultural communities

We acknowledge that CINAC exists as a clinical condition. However, a few words of caution are required when discussing its prevalence. Chronic renal dysfunction inevitably occurs with aging and thus can be regarded as one of the natural changes in physiological function [20, 21]. This is similar to the fact that arteriosclerosis is accompanied by high blood pressure. Accordingly, as the proportion of hypertensive patients increases in the elderly, the prevalence of CKD rises with age. As for the CKD studies reported from various parts of the world, an important point to note is that sample cohort sizes are usually small. Moreover, certain publications do not show the age-stratified or age-adjusted prevalence of CKD (Table 1). CKD is diagnosed based on the positive results of kidney injury and urinary protein tests, each of which is performed twice with a ≥ 3-month interval. However, the majority of epidemiological studies of CKDu have lacked proof of chronicity, failing to strictly differentiate between CKD and AKI [22]. Furthermore, although the diagnosis of CKD in younger patients is commonly established based on a positive proteinuria alone [23], urinalysis results have often not been included in cohort data [24]. The diagnosis of CKD can also be made based on serum creatinine levels. Creatinine is an endogenous metabolic product, and its serum levels are dependent on muscle mass. Consequently, if agricultural workers who participate in clinical studies are physically active and have a high muscle mass, researchers may overestimate the prevalence of CKD.

CKD studies reported from many different locations have shown these kinds of weaknesses in providing scientifically accurate data on prevalence, but have generally shown an increased proportion of CKD patients among young and middle-aged men in agricultural community [24].

Putative etiology of occupational kidney injury related to agriculture

CINAC is defined based on the following patient characteristics [13]: (a) living or working in agricultural communities; (b) a lack of typical risk factors for CKD (including diabetes and hypertension); and (c) low levels of proteinuria. Similar to the clinical features of chronic interstitial nephritis, the kidneys in CINAC patients are small and display a thin cortex with increased echogenicity [13]. Risk factors for CKD identified to date that appear related to agricultural work include: elevated water intake, as a proxy for excessive work hours and/or heat stress [11]; high ambient temperature [25]; heavy metals in soil [3]; agrochemicals (fertilizers and pesticides) [26]; and low-quality drinking water [27] (Fig. 1). CKD is considered to progress at a different pace depending on the degree of exposure to these risk factors [13]. Perspiration from heat stress could conceivably lead to the excessive loss of body fluids (i.e., electrolyte-containing water), resulting in kidney injury. Dehydration can also potentially cause a variety of clinical conditions, including hyperuricemia and rhabdomyolysis. CINAC thus likely arises through combinations of these different pathological processes [28]. However, assuming that kidney injury is caused solely by events triggered by global warming would be unrealistic. In fact, one of the current hypotheses concerning the pathogenesis of CINAC proposes that MeN is associated with high temperatures, while agricultural chemicals are the primary cause of CKDu in South Asia. Some researchers have therefore suggested that CKDu should be called “agrochemical nephropathy”, rather than “global-warming nephropathy” [29,30,31].

Fig. 1
figure 1

Possible mechanisms for the development of kidney injury in agricultural workers. Farmers work outside, and are thus exposed to high temperatures for extended periods of time, particularly in summer. According to epidemiological studies performed in regions known to be CKD hotspots, causes of CKD include: working in the scorching sun, short breaks, inadequate quality and quantity of drinking water, and high levels of exposure to agrochemicals and pesticides. In areas where water quality is poor, easy access to surface water or groundwater suitable for drinking is not always available. This raises the concentrations of agrochemicals and pesticides remaining in the soil and increases their nephrotoxic potential

Currently, no direct evidence suggests that the development of CKD in agricultural workers is associated with exposure to agrochemicals, pesticides, or mixtures of both. However, pathological studies have clearly indicated that kidney injury can be caused by agrochemicals and pesticides contaminated with heavy metals or organic solvents [30]. Moreover, a recent collaborative research demonstrated 34 renal biopsies from Sri Lanka, El Salvador, India and France of patient with CINAC [8]. In addition to usual histopathology of chronic interstitial nephritis, the authors identified a unique constellation of proximal tubular cell including large dysmorphic lysosomes with a light-medium electron-dense matrix in CINAC mainly due to nephrotoxic chemicals. As this feature was also observed in renal histology of calcinurin inhibitor treated transplant patients, they suggested CINAC patients underwent a tubulotoxic mechanism similar to calcineurin inhibitor nephropathy [8]. As climate change persists, water resources (such as rivers and wells) are depleting, and this could lead to higher concentrations of agrochemicals in drinking water [32]. As a result, although the use of potentially harmful agrochemicals and pesticides has recently decreased, agricultural workers and residents in agricultural communities can still be exposed to high levels of chemical compounds that could cause CKDu [33]. Eliminating the risk of CKD thus remains a challenging task.

Need for investigating chronic kidney disease in the agricultural community

From the perspective of industrial health care, scientifically proving that certain occupations are linked to increased risks of specific types of chronic disease is important. For example, heat stress-induced renal dysfunction caused by sugarcane field labor correlates with reductions in crop yields and worker productivity [25]. The results of such analyses could be useful as a basis for the development of, for example, safety measures aimed at protecting workers from solar irradiation. Such data should also prove instrumental for managing work hours suitable for productive business operations. Regarding our society, no direct evidence has been published in Japan regarding changes in the prevalence of CKD, when this disease is considered a health problem associated with temperature increases. However, Japanese agricultural regions evidently will not be spared from global environmental changes. In this context, medical history and the results of health checkup (collectively called medical information) are insufficient for determining the etiology of CKD in previously conducted investigations. For future epidemiological studies in Japan, researchers should establish a more comprehensive analytical method that can incorporate additional risk-factor variables, such as occupational history (including agricultural work), ambient temperature and history of exposures to environmental pollutants.

Conclusion

Based on the clinical features and pathological characteristics identified in agricultural workers from CKD hotspots outside Japan, CINAC clearly represents a genuine public health issue. However, no conclusion has yet been reached regarding whether the prevalence of overall CKD is indeed higher among agricultural communities. This is partly because the epidemiological methodologies used for validating this correlation have sometimes been inadequate. The causes of CINAC include heat stress- and agrochemical-induced kidney injuries, suggesting that complex mechanisms underlie this pathogenesis. Furthermore, the main causes of CINAC appear to vary between different hotspots. In Japan, only a limited number of studies have thus far analyzed the prevalence of CKD in agricultural workers. However, Japanese agricultural regions evidently will not be spared from global warming in the future. It is desirable to practice epidemiological investigation focusing on the environment and occupation.

Availability of data and materials

Not applicable.

Abbreviations

CKD:

Chronic kidney disease

CINAC:

Chronic interstitial nephritis in agricultural communities

MeN:

Mesoamerican nephropathy

AKI:

Acute kidney injury

CKDu:

CKD of unknown etiology

References

  1. Collaboration GBDCKD. Global, regional, and national burden of chronic kidney disease, 1990–2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2020;395(10225):709–33.

    Article  Google Scholar 

  2. Nakai S, Iseki K, Itami N, et al. Overview of regular dialysis treatment in Japan (as of 31 December 2009). Ther Apher Dial. 2012;16(1):11–53.

    Article  Google Scholar 

  3. Lunyera J, Mohottige D, Von Isenburg M, et al. CKD of uncertain etiology: a systematic review. Clin J Am Soc Nephrol. 2016;11(3):379–85.

    Article  CAS  Google Scholar 

  4. Trabanino RG, Aguilar R, Silva CR, et al. End-stage renal disease among patients in a referral hospital in El Salvador. Rev Panam Salud Publica. 2002;12(3):202–6 (in Spanish).

    Article  Google Scholar 

  5. Wesseling C, van Wendel de Joode B, Crowe J, et al. Mesoamerican nephropathy: geographical distribution and time trends of chronic kidney disease mortality between 1970 and 2012 in Costa Rica. Occup Environ Med. 2015;72(10):714–21.

    Article  Google Scholar 

  6. Torres C, Aragon A, Gonzalez M, et al. Decreased kidney function of unknown cause in Nicaragua: a community-based survey. Am J Kidney Dis. 2010;55(3):485–96.

    Article  Google Scholar 

  7. Correa-Rotter R, Wesseling C, Johnson RJ. CKD of unknown origin in Central America: the case for a Mesoamerican nephropathy. Am J Kidney Dis. 2014;63(3):506–20.

    Article  Google Scholar 

  8. Vervaet BA, Nast CC, Jayasumana C, et al. Chronic interstitial nephritis in agricultural communities is a toxin-induced proximal tubular nephropathy. Kidney Int. 2020;97(2):350–69.

    Article  Google Scholar 

  9. Wesseling C, Aragon A, Gonzalez M, et al. Kidney function in sugarcane cutters in Nicaragua—a longitudinal study of workers at risk of Mesoamerican nephropathy. Environ Res. 2016;147:125–32.

    Article  CAS  Google Scholar 

  10. Peraza S, Wesseling C, Aragon A, et al. Decreased kidney function among agricultural workers in El Salvador. Am J Kidney Dis. 2012;59(4):531–40.

    Article  Google Scholar 

  11. Gonzalez-Quiroz M, Pearce N, Caplin B, et al. What do epidemiological studies tell us about chronic kidney disease of undetermined cause in Meso-America? A systematic review and meta-analysis. Clin Kidney J. 2018;11(4):496–506.

    Article  Google Scholar 

  12. Wanigasuriya KP, Peiris-John RJ, Wickremasinghe R, et al. Chronic renal failure in North Central Province of Sri Lanka: an environmentally induced disease. Trans R Soc Trop Med Hyg. 2007;101(10):1013–7.

    Article  Google Scholar 

  13. Jayasumana C, Orantes C, Herrera R, et al. Chronic interstitial nephritis in agricultural communities: a worldwide epidemic with social, occupational and environmental determinants. Nephrol Dial Transplant. 2017;32(2):234–41.

    CAS  PubMed  Google Scholar 

  14. Wijkstrom J, Jayasumana C, Dassanayake R, et al. Morphological and clinical findings in Sri Lankan patients with chronic kidney disease of unknown cause (CKDu): similarities and differences with Mesoamerican nephropathy. PLoS ONE. 2018;13(3):e0193056.

    Article  Google Scholar 

  15. Johnson RJ, Wesseling C, Newman LS. Chronic kidney disease of unknown cause in agricultural communities. N Engl J Med. 2019;380(19):1843–52.

    Article  Google Scholar 

  16. Mani MK. Chronic renal failure in India. Nephrol Dial Transplant. 1993;8(8):684–9 (discussion 3).

    Article  CAS  Google Scholar 

  17. Farag YMK, Karai Subramanian K, Singh VA, et al. Occupational risk factors for chronic kidney disease in Andhra Pradesh: “Uddanam Nephropathy.” Ren Fail. 2020;42(1):1032–41.

    Article  Google Scholar 

  18. Aguilar-Ramirez D, Rana-Custodio A, Villa A, et al. Decreased kidney function and agricultural work: a cross-sectional study in middle-aged adults from Tierra Blanca, Mexico. Nephrol Dial Transpl. 2020. https://doi.org/10.1093/ndt/gfaa041.

    Article  Google Scholar 

  19. El Minshawy O. End-stage renal disease in the El-Minia Governorate, upper Egypt: an epidemiological study. Saudi J Kidney Dis Transpl. 2011;22(5):1048–54.

    PubMed  Google Scholar 

  20. Delanaye P, Glassock RJ, Pottel H, et al. An age-calibrated definition of chronic kidney disease: rationale and benefits. Clin Biochem Rev. 2016;37(1):17–26.

    PubMed  PubMed Central  Google Scholar 

  21. O’Hare AM, Choi AI, Bertenthal D, et al. Age affects outcomes in chronic kidney disease. J Am Soc Nephrol. 2007;18(10):2758–65.

    Article  Google Scholar 

  22. Rigothier C, Chauveau B, Rubin S, et al. Chronic kidney disease of unknown origin in agricultural communities: beyond tropical mist? Nephrol Dial Transpl. 2020. https://doi.org/10.1093/ndt/gfaa265.

    Article  Google Scholar 

  23. Nagai K, Asahi K, Iseki K, et al. Estimating the prevalence of CKD in Japan. Clin Exp Nephrol. 2021. https://doi.org/10.1007/s10157-021-02049-0.

    Article  PubMed  Google Scholar 

  24. Lebov JF, Valladares E, Pena R, et al. A population-based study of prevalence and risk factors of chronic kidney disease in Leon. Nicaragua Can J Kidney Health Dis. 2015;2:6.

    PubMed  Google Scholar 

  25. Dally M, Butler-Dawson J, Krisher L, et al. The impact of heat and impaired kidney function on productivity of Guatemalan sugarcane workers. PLoS ONE. 2018;13(10):e0205181.

    Article  Google Scholar 

  26. Bandara JM, Wijewardena HV, Liyanege J, et al. Chronic renal failure in Sri Lanka caused by elevated dietary cadmium: Trojan horse of the green revolution. Toxicol Lett. 2010;198(1):33–9.

    Article  CAS  Google Scholar 

  27. Chandrajith R, Dissanayake CB, Ariyarathna T, et al. Dose-dependent Na and Ca in fluoride-rich drinking water–another major cause of chronic renal failure in tropical arid regions. Sci Total Environ. 2011;409(4):671–5.

    Article  CAS  Google Scholar 

  28. Johnson RJ, Stenvinkel P, Jensen T, et al. Metabolic and kidney diseases in the setting of climate change, water shortage, and survival factors. J Am Soc Nephrol. 2016;27(8):2247–56.

    Article  Google Scholar 

  29. Herath C, Jayasumana C, De Silva P, et al. Kidney diseases in agricultural communities: a case against heat-stress nephropathy. Kidney Int Rep. 2018;3(2):271–80.

    Article  Google Scholar 

  30. Weaver VM, Fadrowski JJ, Jaar BG. Global dimensions of chronic kidney disease of unknown etiology (CKDu): a modern era environmental and/or occupational nephropathy? BMC Nephrol. 2015;16:145.

    Article  Google Scholar 

  31. Valcke M, Levasseur ME, Soares da Silva A, et al. Pesticide exposures and chronic kidney disease of unknown etiology: an epidemiologic review. Environ Health. 2017;16(1):49.

    Article  Google Scholar 

  32. Nanayakkara S, Senevirathna ST, Abeysekera T, et al. An integrative study of the genetic, social and environmental determinants of chronic kidney disease characterized by tubulointerstitial damages in the North Central Region of Sri Lanka. J Occup Health. 2014;56(1):28–38.

    Article  CAS  Google Scholar 

  33. Jayasumana C, Fonseka S, Fernando A, et al. Phosphate fertilizer is a main source of arsenic in areas affected with chronic kidney disease of unknown etiology in Sri Lanka. Springerplus. 2015;4:90.

    Article  Google Scholar 

  34. Orantes CM, Herrera R, Almaguer M, et al. Chronic kidney disease and associated risk factors in the Bajo Lempa region of El Salvador: Nefrolempa study, 2009. MEDICC Rev. 2011;13(4):14–22.

    Article  Google Scholar 

  35. Wesseling C, Aragon A, Gonzalez M, et al. Heat stress, hydration and uric acid: a cross-sectional study in workers of three occupations in a hotspot of Mesoamerican nephropathy in Nicaragua. BMJ Open. 2016;6(12):e011034.

    Article  Google Scholar 

  36. Athuraliya NT, Abeysekera TD, Amerasinghe PH, et al. Uncertain etiologies of proteinuric-chronic kidney disease in rural Sri Lanka. Kidney Int. 2011;80(11):1212–21.

    Article  Google Scholar 

  37. Fitria L, Prihartono NA, Ramdhan DH, et al. Environmental and occupational risk factors associated with chronic kidney disease of unknown etiology in West Javanese rice farmers, Indonesia. Int J Environ Res Public Health. 2020;17(12):4521.

    Article  CAS  Google Scholar 

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This article was supported, in part, by JSPS Grant No. 18KK0431 and by the Japanese Association of Dialysis Physicians Grant No. 2019-1.

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Correspondence to Kei Nagai.

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Nagai, K. Environment and chronic kidney disease in farmers. Ren Replace Ther 7, 55 (2021). https://doi.org/10.1186/s41100-021-00377-1

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