Evaluation of Cytogenetic Alterations in Patients of Chronic Kidney Disease

Author:

Samarth Ravindra M.12,Tiwari Rajnarayan R.2,Modi Gopesh3,Soni Kishore K.2,Banjare Mohan. L.4,Ul Hasan Shariq1,Jain Sanjay4

Affiliation:

1. ICMR-Department of Research, Bhopal Memorial Hospital and Research Centre (ICMR-BMHRC), Bhopal, Madhya Pradesh, India

2. ICMR-Department of Environmental Health and Epidemiology, National Institute for Research in Environmental Health (ICMR-NIREH), Bhopal, Madhya Pradesh, India

3. Department of Nephrology, Samarpan Super Specialty Clinics, Bhopal, Madhya Pradesh, India

4. Department of Nephrology Kamla Nehru Hospital/Gas Rahat, Bhopal, Madhya Pradesh, India

Abstract

Introduction: In recent years, there has been a rise in chronic kidney disease (CKD), and it has been estimated that by 2040, CKD will be the fifth most common cause of death globally. In addition to diabetes, hypertension, obesity, hyperlipidemia, and nonalcoholic fatty liver disease commonly associated with CKD, exposure to various toxins as a result of pollution or industrial disasters is also discussed as a cause for multi-organ pathology including kidneys. Although few cytogenetic studies were undertaken to assess the genetic damage in survivors of the disaster, no studies are available on the cytogenetic damage of toxic-gas exposed population having CKD. Therefore, the present multi-group cross-sectional study was undertaken to assess the independent role of CKD as well as toxic gas exposure on cytogenetics. Methods: The cytogenetic alterations were evaluated through chromosomal aberration analysis and micronuclei assay. The study included 608 study participants divided into four groups on the basis of history of exposure to the leaked gas and presence or absence of CKD. Results: The results of the study showed no statistically significant difference in cytogenetic damage between gas-exposed and non-exposed patients of CKD, whereas significantly higher cytogenetic damage was observed among gas-exposed participants having CKD compared to gas-exposed participants free from CKD, suggesting that cytogenetic changes could be due to CKD itself. Conclusions: Thus, to conclude, the cytogenetic alterations observed in the study can be partly attributed to the disease itself.

Publisher

Medknow

Subject

Nephrology

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