Feasibility Test of Folic Acid on Acute Kidney Injury

1. Background Information Acute Kidney Injury (AKI) is a worldwide health issue affecting over 13 million people each year with a significant hospital mortality of 20-40%. It is characterized by an abrupt loss of kidney function and is associated with multiple long-term sequelae including chronic kidney disease (CKD) and reliance on renal replacement therapy (RRT). Patients with AKI place a substantial financial burden on healthcare resources. In England, the annual cost of AKI is estimated at £1 billion, consuming 1% of the National Health Service (NHS) budget; in the United States (US), inpatient AKI costs $5 to $24 billion per year. However, there are few therapies to moderate the risk and long-term sequelae of AKI. Timely, efficient treatment of AKI will benefit both patients and health care systems. The National Confidential Enquiry into Patient Outcome and Death (NCEPOD) report on hospital mortality primarily due to AKI judges that good clinical practice occurred in only 50% cases, 33% patients were under insufficient investigations, 29% patients received inadequate clinical management, and complications were badly handled in over 50% cases. Progression of the admission stage of AKI to a higher stage was reported to be associated with a 39% inpatient mortality compared with a 21% mortality in those who did not progress. If the AKI stage could be prevented to deteriorate to a higher stage, the mortality rate of AKI patients during hospital stay would drop almost half. 1.1 Epidemiology, Etiology and Pathophysiology of AKI AKI is a common problem in all countries of the world, and its prevalence has been reported to range from <1% to 66%. Apart from population differences, different classification systems used in epidemiological studies also conduced to the varied estimation of AKI incidence. Little epidemiological data is available for AKI in Hong Kong (HK). Szeto reported a crude hospital admission of AKI of 12% amongst 140,000 hospital admissions observed in a tertiary referral center of HK. The crude mortality rate of AKI in patients attending an emergency department (ED) in HK is 25%. AKI is a multifactorial syndrome. The causes of AKI can be classified into three categories: prerenal, intrinsic renal and postrenal. Prerenal causes involve reduced renal perfusion due to medication, sepsis or volume depletion (e.g., diuretic overuse and diarrhea). Intrinsic renal causes typically result from infections, prolonged hypotension, nephrotoxic drugs or pre-existing renal impairment (e.g., glomerulonephritis and vasculitis). Postrenal AKI is due to obstruction of urinary flow, especially common in elderly men. Sepsis, infection and use of nephrotoxic drugs are common causes of AKI overall, leading to reduced renal blood flow. Sepsis is the most common contributor to AKI (25%). In intensive care unit (ICU) settings, AKI was found to occur in more than half of patients, and half of all patients with AKI in ICU have sepsis. Drug induced AKI occurs in 20% of hospital cases, and those drugs include non-steroidal anti-inflammatory drugs (NSAIDs), metformin, aminoglycosides, angiotensin converting enzyme inhibitors (ACEI), angiotensin II receptor blockers (ARBs), diuretics and iodine containing X-ray contrast. In low-to-middle-income settings, environmental factors such as endemic infections (e.g., malaria and dengue fever) and contaminated water are also common factors to induce AKI. The diverse etiologies of AKI along with other comorbidities make it difficult to determine and understand the pathophysiology of AKI. Recently, oxidative stress has been accepted as the primary mediator of adverse outcomes in AKI, playing a critical role in both initiating and further development of AKI. In the context of deficient renal blood flow in AKI, ischemia-reperfusion represents the most common mechanism in which oxygen and nutrient delivery as well as waste removal are impaired; this mismatch of oxygen supply and demand, and accumulation of waste lead to cellular injury and even death. Sepsis-induced AKI also triggers oxidative stress. Oxidative stress as a key component in the pathophysiology of AKI provides a target for potential therapeutics. Currently, the KDIGO serum creatinine-based criteria is mostly used to stage AKI. The KDIGO defines AKI as either an increase in serum creatinine to ≥1.5 times baseline or ≥0.3 mg/dl (≥26.5 μmol/l) within 48 hours. Depending on the cause and severity of AKI, the clinical presentation of patients with AKI varies. Mild to moderate AKI could be asymptomatic, and severe AKI could present clinical symptoms of uremia. AKI is a rapid (within 48 hours) loss of kidney function, and delays in detection and treatment may contribute to an in-hospital mortality rate of 20-40% that is higher than acute stroke and acute myocardial infarction combined. 1.2 Treatment for AKI Management of AKI is primarily supportive, lacking effective therapeutic drugs. The key to management is assuring hemodynamic stability and preventing hypovolemia in patients so as to ensure sufficient renal perfusion. Depending on the cause and severity of AKI, treatments in hospital usually include: blood pressure and circulating electrolyte control; body fluid balance (e.g., with fluid replacement and/or diuretics); review and cessation of nephrotoxic medication; removing the obstruction if there's a blockage; and use of antibiotics. In severe cases, dialysis may be needed but dialysis is not disease-modifying. Malnutrition is a frequent problem in patients with AKI. Patients should follow a kidney-friendly eating plan to help the kidneys heal, maintain adequate nutrition and restrict potassium. There are no approved pharmacological agents for treating AKI. 1.3 Folate Folic acid is a common external supplement of folate (Vitamin B9). Folic acid is a synthetic, parent compound of folate family. Folic acid gets metabolized into 5-methyltetrahydrofolate (5-MTHF). 5-MTHF is the biologically active form of folate and the predominant form of dietary folate in plasma. A systematic review was conducted in accordance with the PRISMA guidelines and registered in PROSPERO (CRD42024589377). The investigators searched six databases (PubMed, MEDLINE, CINAHL, CENTRAL, Embase, and Web of Science) from their inception until March 2024, identifying 36 randomized controlled trials (RCTs) that evaluated folate use in patients with CKD or AKI. Of these, 22 RCTs compared folate use with no use in patients with CKD, with treatment durations ranging from 4 weeks to 4.5 median years, and majority use folic acid. Notably, no published data focused on AKI populations. Among included RCTs, 20 reported that folate use significantly reduced homocysteine (Hcy) levels but not directly reduced cardiovascular events in CKD patients. Only 5 trials assessed markers of kidney disease progression including 3 measured serum creatinine and 2 measured estimated glomerular filtration rate (eGFR) with inconsistent findings. The largest study, China Stroke Primary Prevention Trial with 1671 CKD patients, demonstrated that folate use slowed the annual decline in eGFR compared to controls (0.96 ± 5.81% vs. 1.72 ± 6.08%, respectively). Similarly, a modest reduction in serum creatinine was observed in end-stage renal disease (ESRD) patients receiving folate (10.94 ± 2.01 vs. 11.30 ± 2.31 in controls). Safety analyses across all 22 RCTs revealed no severe adverse events attributable to folate, and no significant differences in adverse outcomes were noted between the treatment and control groups. Low doses: In a rat model of AKI with ischemia-reperfusion, 5-MTHF at a low dose of 3 μg/kg body weight improved kidney function, reduced plasma creatinine levels and alleviate oxidative stress within 24 hours. The expression of neutrophil gelatinase-associated lipocalin (NGAL), a marker of proximal tubular injury, was significantly reduced after folate treatment. 5-MTHF activated the nuclear factor erythroid 2-related factor 2 (Nrf2), a key regulator of the antioxidant defense system. Nrf2 activation regulates gene expression of detoxification enzymes and antioxidant proteins, which is vital to restore antioxidant defense against oxidative stress injury. Oxidative stress is the mainstay responsible to the adverse outcomes in AKI. The expression of antioxidant enzymes, superoxide dismutase-1 (SOD-1), glutathione synthesizing enzymes and heme oxygenase-1 (HO-1), were all upregulated after folate treatment. High doses: Folic acid, a precursor of folate, at high doses, e.g., 250 mg/ /kg body weight, has been used to induce AKI in animals. Folic acid causes AKI due to the rapid onset of folic acid crystals within renal tubules with a subsequent acute tubular necrosis, epithelial regeneration and renal cortical scarring. High concentrations of folic acid will lead to oxidative stress, mitochondrial abnormalities, ferroptosis, pyroptosis and increased expression of fibroblast growth factor 23 (FGF23). However, folic acid induced AKI is only experimental in animals, and high levels of folic acid have not been observed in the clinic kidney diseases. 1.4 Unmet Clinical Need AKI is a common health issue with high morbidity and mortality in hospital. Delays in detection and treatment result in an in-hospital mortality rate of 20-40% that is higher than acute stroke and acute myocardial infarction combined. Management of AKI is primarily supportive. There are no approved pharmacological agents for treating AKI. Oxidative stress provides a target for therapeutics. Animal experiments have shown folate IN LOW DOSES alleviated oxidative stress, decreased plasma creatinine levels and improved kidney function of AKI. Folate administration has been studied to improve survival of patients with CKD using randomized clinical trials. Evidence for the protective effect of folate against AKI to safely reduce circulating creatinine levels, progression to CKD/ESRD and mortality in adult patients with AKI is needed. 1.5 Impact If folate treatment improved outcome for 1% cases, as the global burden of AKI per year is 13 million cases, then potentially 130,000 patients could benefit per year; in HK, as AKI identified with a crude hospital admission of 12%, among around 2 million hospital admissions in one year, potentially 2,500 patients could benefit per year.
2. Aims and Hypotheses 2.1 Aims This study aims to evaluate the folate intervention feasibility in adult patients with AKI, and the possibility of conducting a future fully powered RCT. The investigators propose to conduct this feasibility study among adults with AKI receiving usual care in the ED, ICU and medical wards at Queen Mary Hospital (QMH). 2.2 Hypotheses The hypotheses of this study are set as meeting the feasibility criteria: ≥70% of patients recognized as eligible by clinicians are randomly allocated to study arm of which ≥70% of patients complete 90% or greater of the course of treatment and less than 5% adverse events (AEs) difference between no supplement control and folate supplement arms.
3. Plan of Investigation

This is a feasibility study with an open-label, randomized, 1:1 ratio (Usual care vs. 5 mg folic acid + Usual care).

This study will be conducted in accordance with Good Clinical Practice (GCP) guidelines and reported in accordance with the Consolidated Standards of Reporting Trials (CONSORT) statement.

3.1 Screening, recruitment and consent The investigators will check hospital records and the Clinical Management System (CMS) to identify potential participants. Then, the investigators will use a screening form to determine the eligibility of potential participants, and review their medical records. Eligible patients will be informed the study and asked for the consent to participate.

3.2 Randomization An investigator with no clinical involvement in the trial will do block randomization. The two study arms of control, and 5 mg/d folate will be allocated according to the randomization orders.

The study information and medications will be put into sealed envelopes. The outside of the envelope will contain the name of the study and possible arms contained within, but not which arm is selected. Each enrolled patient will be assigned an order number and receive the corresponding envelope. The patient ID, date, time and other information will be recorded on the envelope. Once the patients completed all baseline assessments, they will be allocated the treatment. In the case of broken or lost envelopes, the researcher figures out what the number of the envelope it is and replaces the envelope with the same treatment according to the allocation.

Hospital clinicians are responsible for administration of the allocated treatment. The patient's own doctors are free to modify or stop study treatment if they feel that it is in the best interests of the patient without the need for the patient to withdraw from the study.

3.3 Data collection An admission log, blood tests, investigations, medication review, and adverse events will be recorded for every patient. Screening form and consent form will be recorded for every patient. A member of the hospital clinical or research staff (as appropriate/designated) will collect this information and enter it into an IT system. The investigators will collect patient information before randomization and follow up daily for up to 30 days. Additional follow-ups will be conducted at 3 months and one year by contacting patients on the ward, in an outpatient setting, by phone or via their electronic record. Personal information and study data will be kept for 3 years after the completion of the study.