

What is the Living Kidney Donor Safety Study?
The Living Kidney Donor (LKD) Safety Study is a multicenter prospective cohort study that looked at the long-term effects of becoming a kidney donor. A total of 17 transplant centres across Canada and Australia recruited study participants. At these centres, the study team recruited living kidney donors, controls (study buddies) and recipients into the study. The trial was conducted to better understand:
- The long-term health outcomes of living kidney donors, including:
- High blood pressure,
- High levels of protein (or albumin) in the urine (albuminuria) and
- Long-term kidney function (eGFR).
- The psychological effects of living kidney donation.
- The financial costs of living kidney donation evaluation.
- Living kidney donor factors which influence recipient outcomes.

The study’s primary findings were published in the Journal of the American Medical Association on May 23, 2024.
Why was this study needed?
A kidney transplant from a living donor is considered safe in healthy adults. Furthermore, it is the best treatment option for most patients with kidney failure. Receiving a kidney transplant from a living donor typically results in superior rates of graft survival and shorter wait times compared to a kidney transplant received from a deceased donor. Yet, the kidney transplant community, including donors, recipients, and potential donors, need to better understand the long-term effects of donation.
The Study’s Methods
Between 2004 and 2014, the LKD Safety Study team recruited 1042 living donors (924 standard criteria donors and 118 donors with isolated medical abnormalities), 396 non-donor participants and 824 kidney recipients to participate in a study focused on determining the long-term outcomes for living kidney donors. Specifically, the study looked at the donor’s risk of developing high blood pressure or albuminuria, and the rate of kidney function decline in the decade following donation. The study also examined changes in the participants’ quality of life. This includes medical, financial, and psychological implications of living kidney donation.

During the study, the team collected annual blood pressure measurements, health and psycho-social questionnaires, and kidney function lab results from each participant, including initial baseline data in 2004 and 9576 annual follow-up visits held between 2005 to 2021. The study team analyzed the data with a focus on improving the transplant decision-making process, informed consent, health policies and the follow-up of living donors to keep them in good health.
The Living Kidney Donor Safety Study Findings
The LKD Safety Study collected data from participants for more than a decade. After completing the data analysis, the study team found that living donors have a similar risk of developing high blood pressure and albuminuria as non-donors. There is also no greater rate of kidney function decline after the initial drop and recovery of kidney function following surgery between donors and non-donors.
Specifically, high blood pressure occurred in 17% of donors and non-donors and the change in average blood pressure over a decade (median of 7.3 years) was similar between the groups. Additionally, donors reported lower physical health than non-donors in the first 3 months after surgery, but similar physical health in all follow-up annual questionnaires in subsequent years. The LKD Safety Study team found no other clinically relevant difference in health-related quality of life, anxiety, or depression during follow-up.
Read the team’s findings
LKD Safety Study Newsletter
LKD Safety Study Clinical Findings
Étude sur la sécurité des donneurs vivants de reindonneurs vivants de rein (LKD Safety Study Newsletter -FR)

Thank you to our participants
The LKD Safety Study team would like to thank all our study participants for participating in this study. We greatly appreciate all your time and effort over the years. Above all, your dedication to finding answers about long-term outcomes for living kidney donors has allowed us to complete this study and improve our understanding of the long-term effects of donating a kidney.
LKD Safety Study Resources and Media

Media
- Hypertension and Kidney Function After Living Kidney Donation – JAMA Peer-Review Article
- Outcomes After Living Kidney Donation – JAMA Podcast interview with Dr. Amit X. Garg.
Living Kidney Donor Safety Study Participating Centres
Canadian Centres
- St Paul’s Hospital (Vancouver, BC)
- University Health Network (Toronto, ON)
- London Health Sciences Centre (London, ON)
- University of Alberta (Edmonton, AB)
- Ottawa Hospital (Ottawa, ON)
Vancouver General Hospital (Vancouver, BC) - St. Michael’s Hospital (Toronto, ON)
- Foothills Medical Centre (Calgary, AB)
- Royal Victoria Hospital (Montreal, QC)
- Queen Elizabeth II Hospital (Halifax, NS)
- Health Sciences Centre (Winnipeg, MB)
- St. Joseph’s Hospital (Hamilton, ON)
Australian Centres
- Sir Charles Gairdner Hospital (Peth, Western Australia)
- Monash Medical Centre (Clayton, Victoria)
- Royal Perth Hospital (Perth, Western Australia)
- Freemantle Hospital (Freemantle, Western Australia)
- Royal Adelaide Hospital (Adelaide, South Australia)
Publications from the LKD Safety Study
Meet our Team!

Dr. Amit Garg, MD, FRCPC, FACP, MEd, PhD, Associate Dean, Professor
Dr. Amit Garg is the Principal Investigator for the LKD Safety Study since it began in 2009. He holds the role of the Associate Dean for Clinical Research, at the Schulich School of Medicine & Dentistry, a Professor of Medicine and Epidemiology & Biostatistics at Western University, and is also an internationally recognized nephrologist and clinical scientist.
Dr. Garg serves as a staff nephrologist with London Health Sciences Centre, Scientist with the Lawson Health Research Institute, and Scientist with ICES. He is also the Program Lead for the ICES Kidney, Dialysis & Transplantation Provincial Research Program and the former Site Director of the ICES Western facility in London, Ontario. Dr. Garg conducts clinical and health services research to improve health outcomes for patients with chronic kidney disease. He is currently focused on large pragmatic trials and is developing a pragmatic trial training program.

Jennifer Arnold BA, BSc
Jennifer Arnold has been the Canadian national research coordinator for the LKD Safety Study since it began in 2009. She has a background in biology (2008), political science (1998) and clinical trials management (2009). Ms. Arnold began working on LKD projects with Dr. Garg in 2005 which included both the retrospective and pilot versions of the current large multicenter prospective cohort LKD Study.
Ms. Arnold also currently coordinates and assists with other non-LKD related studies and activities (i.e. grant applications). In her role as a research coordinator, Ms. Arnold coordinates and monitors all the research activities (study recruitment, data collection, data cleaning, study site management, regulatory paper work, sample collection, etc.) that a study may require until its completion.

Meaghan Cuerden-Knight – PhD
Dr. Meaghan Cuerden-Knight has been a biostatistician with London Health Sciences Centre since 2007 and has worked as a study statistician for the LKD Safety Study since 2007, before the start of the study. She has a background in biostatistics. Dr. Cuerden-Knight began working with Dr. Garg in 2007 and has focused her work on study planning, data cleaning, and data analysis. She is grateful for the opportunity to work on this important project.
Dr. Cuerden-Knight is a mom of three and is grateful for the opportunity to work on this important project.
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Sponsors

For further information or to obtain a copy of the publication, please contact LKDStudy@lhsc.on.ca.
The medical information on this site is provided as an information resource only, and is not to be used or relied on for any diagnostic or treatment purposes. This information does not create any patient-physician relationship, and should not be used as a substitute for professional advice, diagnosis and/or treatment.