About Careers MedBlog Contact us
Medindia LOGIN REGISTER
Advertisement

DNA Testing may Soon be Routine for Patients with Kidney Disease

by Iswarya on December 27, 2018 at 1:10 PM
Font : A-A+

DNA Testing may Soon be Routine for Patients with Kidney Disease

Genes are responsible for about 1 in 10 cases of chronic kidney disease in adults, and identifying the responsible gene has an immediate impact on treatment for most of these patients. The findings of the study are published in the New England Journal of Medicine.

"Our study shows that genetic testing can be used to personalize the diagnosis and management of kidney disease and that nephrologists should consider incorporating it into the diagnostic workup for these patients," says Ali Gharavi, MD, chief of nephrology at Columbia University Vagelos College of Physicians and Surgeons, and a co-senior author of the study.

Advertisement


It's estimated that 1 in 10 adults in the United States has chronic kidney disease. Yet, for 15 percent of patients with chronic kidney disease, the underlying cause of kidney failure is unknown.

"There are multiple genetic causes of chronic kidney disease, and treatment can vary depending on the cause," says Gharavi. "But many of the genetic types are rare and can be difficult to detect with traditional diagnostics.
Advertisement

And because kidney disease is often silent in the early stages, some patients aren't diagnosed until their kidneys are close to failing, making it more difficult to find the underlying cause."

DNA sequencing has the potential to pinpoint the genetic culprits but has not been tested in a wide range of patients with chronic kidney disease.

"Our study identifies chronic kidney disease as the most common adult disease, outside of cancer, for which genomic testing has been demonstrated as clinically essential," says David Goldstein, Ph.D., director of Columbia University's Institute for Genomic Medicine and a co-senior author of the study.

In this study, researchers used DNA sequencing to look for genetic kidney disorders in 3,315 individuals with various types of chronic or end-stage kidney disease. For 8.5 percent of these individuals, clinicians had not been able to identify the cause of disease.

The researchers found a genetic disorder responsible for about 9 percent of the participants' kidney problems, and DNA testing reclassified the cause of kidney disease in 1 out of 5 individuals with a genetic diagnosis. Also, DNA testing was able to pinpoint a cause for 17 percent of participants for whom the diagnosis was not possible based on the usual clinical workup.

DNA results had a direct impact on clinical care for about 85 percent of the 168 individuals who received a genetic diagnosis and had medical records available for review. "For several patients, the information we received from DNA testing changed our clinical strategy, as each one of these genetic diagnoses comes with its own set of potential complications that must be carefully considered when selecting treatments," Gharavi says.

About half of the patients were diagnosed with a kidney disorder that also affects other organs and requires care from other specialists. A few (1.5 percent) individuals learned they had medical conditions unrelated to their kidney disease; In all of these cases, the incidental findings had an impact on kidney care. "For example, having a predisposition to cancer would modify the approach to immunosuppression for patients with a kidney transplant," adds Gharavi.

"These results suggest that genomic sequencing can optimize the development of new medicines for kidney disease through the selection of patient subgroups most likely to benefit from new therapies," says Adam Platt, Ph.D., Head of Global Genomics Portfolio at AstraZeneca and a co-senior author of the study.

While the current study shows the utility of DNA testing in people with kidney disease, another study led by Goldstein and Gharavi found that DNA testing in healthy individuals vastly overestimated the prevalence of kidney disease-associated genetic conditions.

"Altogether, our research suggests that DNA testing may be most useful when balanced with clinical information," says Goldstein.

Source: Eurekalert
Advertisement

Advertisement
Advertisement

Recommended Reading

Latest Genetics & Stem Cells News

 Stem Cell Treatment Resolves Perianal Fistulas in Crohn's Disease
Can stem cell therapy cure fistula? Yes, treatment with stem cells has had a success rate when used in perianal fistulas due to Crohn's Disease.
First Effective Preclinical Models for Most Common Genetic Cause of Leigh Syndrome
In zebrafish models of SURF1 mitochondrial disease, scientists have discovered drugs to prevent neurological decompensation.
Gene Therapy for Rare Eye Disease
New study advances intravitreal gene therapy platform to develop safe and effective therapies for visual loss in Usher Syndrome, rare disorder.
Autism-associated Mutation: New Insights
The study experiments shed light on a rare example of how autism-associated mutation could altered nuclear dynamics.
How Genomic Variants Could Help Diagnose Rare Genetic Disorders
A genotype-first approach to patient care involves selecting patients with specific genomic variants and then studying their traits and symptoms.
View All
This site uses cookies to deliver our services.By using our site, you acknowledge that you have read and understand our Cookie Policy, Privacy Policy, and our Terms of Use  Ok, Got it. Close
×

DNA Testing may Soon be Routine for Patients with Kidney Disease Personalised Printable Document (PDF)

Please complete this form and we'll send you a personalised information that is requested

You may use this for your own reference or forward it to your friends.

Please use the information prudently. If you are not a medical doctor please remember to consult your healthcare provider as this information is not a substitute for professional advice.

Name *

Email Address *

Country *

Areas of Interests