Should a dialysis patient with end-stage renal disease and a normal folic acid level discontinue folic acid supplementation?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: January 27, 2026View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Discontinue Folic Acid Supplementation in This Dialysis Patient

Yes, you should discontinue folic acid supplementation in this dialysis patient with a normal folic acid level of 25 ng/mL, as the level is well above the normal range and continued supplementation provides no cardiovascular benefit while carrying potential risks. 1

Rationale for Discontinuation

Normal Folate Status Achieved

  • Your patient's folic acid level of 25 ng/mL exceeds the normal reference range (3-16 ng/mL), indicating adequate to supraphysiologic folate stores 1
  • The 2020 KDOQI guidelines specifically recommend folic acid supplementation only to correct documented folate or vitamin B12 deficiency/insufficiency based on clinical signs and symptoms 1
  • Once folate levels normalize, maintenance supplementation should be reduced to approximately 330 mcg DFE (dietary folate equivalents) for adults, which can typically be achieved through diet and standard multivitamin supplementation 1

No Cardiovascular Benefit from Continued Supplementation

  • The 2020 KDOQI guidelines provide a Grade 1A recommendation (the strongest level) against routinely supplementing folate for hyperhomocysteinemia in dialysis patients, as there is no evidence demonstrating reduction in adverse cardiovascular outcomes 1
  • This represents a critical shift from older practices that emphasized homocysteine lowering 1
  • Even though folic acid reduces homocysteine levels by approximately 35-40% in dialysis patients, this biochemical change does not translate into improved clinical outcomes 2, 3

Potential Risks of Excessive Supplementation

  • The FDA label warns that folic acid doses above 0.1 mg daily may obscure pernicious anemia by correcting hematologic abnormalities while allowing neurologic manifestations to progress 4
  • The established upper tolerable limit (UL) for folic acid is 1 mg/day, set specifically to avoid delayed diagnosis of vitamin B12 deficiency and minimize risk of neurological complications 1
  • Concerns exist regarding potential proliferative effects, insulin resistance, drug interactions (particularly with anticonvulsants), and hepatotoxicity at excessive doses 1

Recommended Management Approach

Immediate Action

  • Discontinue the current folic acid supplement 1
  • Ensure the patient receives a standard renal multivitamin that contains water-soluble vitamins at appropriate maintenance doses 1

Monitoring Strategy

  • Recheck folate levels in 3-6 months after discontinuation to ensure levels remain adequate but not excessive 1
  • The 2022 ESPEN guidelines recommend measuring folate status every 3 months until stabilization, then annually in diseases with increased folate needs 1
  • Monitor for any clinical signs of folate deficiency (macrocytic anemia, glossitis, neurological symptoms), though this is unlikely given the elevated baseline level 1

Long-term Maintenance

  • Standard renal multivitamins typically provide adequate water-soluble vitamin replacement for dialysis losses 1
  • If folate levels drop below normal range (typically <3 ng/mL) with clinical manifestations, consider resuming supplementation at 1-5 mg orally per day for 4 months, then reassess 1
  • The 2022 ESPEN guidelines note that in chronic hemodialysis patients with hyperhomocysteinemia, 5 mg or more per day may be required for non-diabetic patients and 15 mg per day for diabetic patients, but this is for documented deficiency states, not routine supplementation 1

Common Pitfalls to Avoid

  • Do not continue supplementation simply because the patient is on dialysis - the indication is deficiency correction, not routine prophylaxis for cardiovascular risk reduction 1
  • Do not use homocysteine levels as a target for folic acid dosing - lowering homocysteine does not improve cardiovascular outcomes in this population 1
  • Ensure vitamin B12 status is also assessed - folate supplementation can mask B12 deficiency, which is common in dialysis patients and requires separate treatment 1, 4
  • Verify the patient is receiving adequate dietary protein (60-80g/day) - this typically provides 120-260 mcg of dietary folic acid, which may be sufficient without supplementation in well-nourished patients 5

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Sustained reduction of hyperhomocysteinaemia with folic acid supplementation in predialysis patients.

Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, 1999

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.