TY - JOUR
T1 - Potential Mechanisms Involved in Chronic Kidney Disease of Unclear Etiology
AU - Holliday, Michael W.
AU - Li, Qingtian
AU - Bustamante, Edlyn G.
AU - Niu, Jingbo
AU - Huang, Luping
AU - Espina, Ilse M.
AU - Dominguez, Jose R.
AU - Truong, Luan
AU - Murray, Kristy O.
AU - Fan, Lei
AU - Anumudu, Samaya J.
AU - Shah, Maulin
AU - Fischer, Rebecca S.B.
AU - Vangala, Chandan
AU - Mandayam, Sreedhar
AU - Perez, Jose
AU - Pan, Jenny S.
AU - Ali, Sehrish
AU - Awan, Ahmed A.
AU - Sheikh-Hamad, David
N1 - Funding Information:
Biomedical Laboratory Research and Development Program career development award BX002912 (to J.S. Pan) and merit award BX002006 (to D. Sheikh-Hamad). M. Shah reports employment with the Michael E. DeBakey Veteran’s Affairs Medical Center and research funding from Leonard-Meron Biosciences for an industry-sponsored clinical trial. All remaining authors have nothing to disclose.
Funding Information:
We acknowledge the generous support of Dr. and Mrs. Harold Selzman through the Selzman Institute for Kidney Health. The Nicaragua Sugar Estates, LTD Scientific Advisory Board and its affiliates played no direct role in this study. The contents of this manuscript do not represent the views of the US Department of Veterans Affairs or the US Government.
Funding Information:
R.S.B. Fischer is supported by National Institutes of Health grant 5K01TW010863 from the Fogarty International Center. Salary support to M.W. Holliday was provided by the American Society of Nephrology Foundation for Kidney Research George B. Rath-mann research fellowship award as part of the Ben J. Lipps Research Fellowship Program. Salary support to K.O. Murray was provided by the El Comité Nacional de Productores de Azúcar de Nicaragua. Salary support was provided by US Department of Veterans Affairs Biomedical Laboratory Research and Development Program career development award BX002912 (to J.S. Pan) and merit award BX002006 (to D. Sheikh-Hamad).
Funding Information:
S.J. Anumudu reports employment with Exxon; occasional honoraria from St. George’s University for helping with student information events or webinars as a student counselor and the alumni admissions mentor program; and serving as an American Society of Nephrology Public Policy Committee Member and as a Renal Physicians Association board member, government affairs vice chair, and membership and education committee member (all roles are unpaid). E.G. Bustamante reports employment with Harris Health System. R.S.B. Fischer reports employment with Exxon Mobil and support from the National Institutes of Health grant 5K01TW010863 from the Fogarty International Center. S. Man-dayam reports consultancy agreements with Chinook and Sanofi; ownership interest in Medingenii Capital LLC and Prosalus Capital LLC; research funding from Alexion, Equillium, Goldfinch Bio, Novartis, Omeros, Pfizer, Roche, Travere, and Vertex; speakers bureau for Alexion, Bayer, and Otsuka; and other interests or relationships with the Mandayam Family Foundation and Unicef USA. K. Murray reports consultancy agreements with Valneva Corporation and serving on the Nicaragua Sugar Estates, LTD Scientific Advisory Board. Salary support to K. Murray was provided by the El Comité Nacional de Productores de Azúcar de Nicaragua. D. Sheikh-Hamad, M.W. Holliday, and J.S. Pan report employment with Michael E. DeBakey Veteran’s Affairs Medical Center. Salary support was provided by US Department of Veterans Affairs
Publisher Copyright:
© 2022 by the American Society of Nephrology.
PY - 2022/9
Y1 - 2022/9
N2 - Background and objectives The etiology of chronic kidney disease of unclear etiology, also known as Mesoamerican nephropathy, remains unclear. We investigated potential etiologies for Mesoamerican nephropathy in an immigrant dialysis population. Design, setting, participants, & measurements Migrants with Mesoamerican nephropathy kidney failure (n552) were identified by exclusion of known causes of kidney disease and compared using a cross-sectional survey with demographically similar patients with kidney failure from other causes (n563) and age/sex/place of origin–matched healthy participants (n516). Survey results were extended to the bench; C57BL/6 mice (n573) received 10–15 weekly intraperitoneal injections of paraquat (a reactive oxygen species–generating herbicide) or vehicle. Kidney function, histology, and expression of organic cation transporter-2 (proximal tubule entry for paraquat) and multidrug and toxin extrusion 1 (extrusion pathway) were examined. Kidney biopsies from Nicaraguan patients with acute Mesoamerican nephropathy were stained for the above transporters and compared with patients with tubulointerstitial nephritis and without Mesoamerican nephropathy. Results Patients with Mesoamerican nephropathy and kidney failure were young agricultural workers, almost exclusively men; the majority were from Mexico and El Salvador; and they had prior exposures to agrochemicals, including paraquat (27%). After adjustment for age/sex, exposure to any agrochemical or paraquat was associated with Mesoamerican nephropathy kidney failure (odds ratio, 4.86; 95% confidence interval, 1.82 to 12.96; P50.002 and odds ratio, 12.25; 95% confidence interval, 1.51 to 99.36; P50.02, respectively). Adjusted for age/sex and other covariates, 1 year of agrochemical exposure was associated with Mesoamerican nephropathy kidney failure (odds ratio, 1.23; 95% confidence interval, 1.04 to 1.44; P50.02). Compared with 16 matched healthy controls, Mesoamerican nephropathy kidney failure was significantly associated with exposure to paraquat and agrochemicals. Paraquat-treated male mice developed kidney failure and tubulointerstitial nephritis consistent with Mesoamerican nephropathy. Organic cation transporter-2 expression was higher in male kidneys versus female kidneys. Paraquat treatment increased organic cation transporter-2 expression and decreased multidrug and toxin extrusion 1 expression in male kidneys; similar results were observed in the kidneys of Nicaraguan patients with Mesoamerican nephropathy. Conclusions Exposure to agrochemicals is associated with Mesoamerican nephropathy, and chronic exposure of mice to paraquat, a prototypical oxidant, induced kidney failure similar to Mesoamerican nephropathy.
AB - Background and objectives The etiology of chronic kidney disease of unclear etiology, also known as Mesoamerican nephropathy, remains unclear. We investigated potential etiologies for Mesoamerican nephropathy in an immigrant dialysis population. Design, setting, participants, & measurements Migrants with Mesoamerican nephropathy kidney failure (n552) were identified by exclusion of known causes of kidney disease and compared using a cross-sectional survey with demographically similar patients with kidney failure from other causes (n563) and age/sex/place of origin–matched healthy participants (n516). Survey results were extended to the bench; C57BL/6 mice (n573) received 10–15 weekly intraperitoneal injections of paraquat (a reactive oxygen species–generating herbicide) or vehicle. Kidney function, histology, and expression of organic cation transporter-2 (proximal tubule entry for paraquat) and multidrug and toxin extrusion 1 (extrusion pathway) were examined. Kidney biopsies from Nicaraguan patients with acute Mesoamerican nephropathy were stained for the above transporters and compared with patients with tubulointerstitial nephritis and without Mesoamerican nephropathy. Results Patients with Mesoamerican nephropathy and kidney failure were young agricultural workers, almost exclusively men; the majority were from Mexico and El Salvador; and they had prior exposures to agrochemicals, including paraquat (27%). After adjustment for age/sex, exposure to any agrochemical or paraquat was associated with Mesoamerican nephropathy kidney failure (odds ratio, 4.86; 95% confidence interval, 1.82 to 12.96; P50.002 and odds ratio, 12.25; 95% confidence interval, 1.51 to 99.36; P50.02, respectively). Adjusted for age/sex and other covariates, 1 year of agrochemical exposure was associated with Mesoamerican nephropathy kidney failure (odds ratio, 1.23; 95% confidence interval, 1.04 to 1.44; P50.02). Compared with 16 matched healthy controls, Mesoamerican nephropathy kidney failure was significantly associated with exposure to paraquat and agrochemicals. Paraquat-treated male mice developed kidney failure and tubulointerstitial nephritis consistent with Mesoamerican nephropathy. Organic cation transporter-2 expression was higher in male kidneys versus female kidneys. Paraquat treatment increased organic cation transporter-2 expression and decreased multidrug and toxin extrusion 1 expression in male kidneys; similar results were observed in the kidneys of Nicaraguan patients with Mesoamerican nephropathy. Conclusions Exposure to agrochemicals is associated with Mesoamerican nephropathy, and chronic exposure of mice to paraquat, a prototypical oxidant, induced kidney failure similar to Mesoamerican nephropathy.
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U2 - 10.2215/CJN.16831221
DO - 10.2215/CJN.16831221
M3 - Article
C2 - 35944911
AN - SCOPUS:85137605167
SN - 1555-9041
VL - 17
SP - 1293
EP - 1304
JO - Clinical Journal of the American Society of Nephrology
JF - Clinical Journal of the American Society of Nephrology
IS - 9
ER -