Clinical Trial Details
— Status: Recruiting
Administrative data
NCT number |
NCT06105229 |
Other study ID # |
NO.GDREC2020278H |
Secondary ID |
|
Status |
Recruiting |
Phase |
|
First received |
|
Last updated |
|
Start date |
August 1, 2022 |
Est. completion date |
June 2024 |
Study information
Verified date |
October 2023 |
Source |
Guangdong Provincial People's Hospital |
Contact |
zhilian li, doctor |
Phone |
13580560903 |
Email |
lizhilian[@]gdph.org.cn |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
The goal of this observational study is to assess the clinical value of humanin in acute
kidney injury. The main questions it aims to answer are:whether Humanin can be a novel marker
for predicting AKI Researchers will compare humanin concentration in healthy people to see if
humanin can be a novel marker for predicting AKI
Description:
Acute Kidney Injury (AKI) is a clinically critical condition manifested by a sharp decline in
kidney function, with approximately 13.3 million people diagnosed with AKI each year in
hospital worldwide and associated with 1.7 million deaths. According to global multi-center
research data, the total incidence of AKI in hospital is as high as 21%, and the incidence of
acute kidney injury in hospitalized patients in China is 0.99%~11.6%. AKI increases the risk
of long-term chronic kidney disease (CKD) and end-stage renal disease (ESRD), and has a very
high long-term mortality rate. The diagnosis of AKI is mainly based on blood creatinine or
urine output, and the current KDIGO criteria are used, but blood creatinine is a very
insensitive indicator, so in the past 20 years, scholars have been exploring biological
markers that are more sensitive than blood creatinine and urine output. Humanin is a
mitochondrial polypeptide containing 24 amino acids. It was first identified in Alzheimer's
disease patients in 2001. Studies have shown that Humanin has a strong mitochondrial
protective effect in neurodegenerative diseases, cardiovascular diseases, diabetes, male
infertility, cancer and other diseases, and its mechanism may be related to anti-apoptosis,
anti-inflammation, regulation of autophagy and maintenance of mitochondrial homeostasis,
because Humanin can function through autocrine, paracrine or endocrine forms, so it can be
detected in the blood. Studies have shown that Humanin expression in serum or plasma of
patients with diabetes and coronary heart disease is declined. In our previous study, the
investigators found that Humanin was elevated in plasma in a mouse model of AKI with sepsis.
The goal of this observational study is to assess the clinical value of humanin in acute
kidney injury. The main questions it aims to answer are:whether Humanin can be a novel marker
for predicting AKI