HomeAnswersMedical GastroenterologybilirubinWhy is my bilirubin level a bit higher?

Is it fine to have a bit higher bilirubin level?

Share

The following is an actual conversation between an iCliniq user and a doctor that has been reviewed and published as a Premium Q&A.

Medically reviewed by

iCliniq medical review team

Published At April 2, 2018
Reviewed AtJanuary 17, 2024

Patient's Query

Hello doctor,

I am a 29-year-old male, weigh 198.4 lbs , height is 5 feet 9 inches, non-smoker, non-alcohol drinker. I do not have any symptoms or signs, normal eye, and skin color. I am taking Cipralex 15 mg for the past one year. Had a history of bladder stone and it required admission for one week until it passed normally by medications without surgical intervention. When I reviewed my blood test results, I found out the bilirubin level is bit higher than normal. I was overthinking, so I kept repeating the test weekly. What do you think of my case? Could we consider bilirubin high? If yes, what might be the causes?

Answered by Dr. Babu Lal Meena

Hi,

Welcome to icliniq.com.

If Mmol means micron mol, then it is fine (attachment removed to protect patient identity). It looks like a normal variant of hyperbilirubinemia. Most common cause of the condition is hemolysis, Gilbert syndrome is also a common cause of such a situation. In both the conditions, we find the unconjugated bilirubin. I hope your urine is not yellow.

Another issue is you have high BMI. It is obesity. So, you may have a fatty liver disease, that could be the cause of high ALT. I want to do a fibroscan and repeat ultrasound for fatty liver and TATA box mutation for Gilbert syndrome and reticulocyte counts with smear examination and G6PD level in blood. Rest of the workup you have already done. You may provide the complete reports of the investigation, including the previous investigation. So it will be good for us and help to interpret.

The Probable causes

Hemolysis (thalassemia variant or G6PD deficiency), Gilbert syndrome, fatty liver disease.

Investigations to be done

Do fibroscan and repeat ultrasound for fatty liver. TATA box mutation for Gilbert syndrome, reticulocyte counts with smear examination and G6PD level in blood, liver function tests, fasting blood glucose, HbA1c.

Differential diagnosis

Hemolysis (thalassemia variant or G6PD deficiency), Gilbert syndrome, fatty liver disease.

Treatment plan

Provide the reports. Do regular exercise, at least 1 to 2 hours a day. A low-fat diet. Target weight is 75 to 80 kg, lose 5 kg in the next three months. Stop alcohol, if you are addicted to that. Capsule Vitamin E, 400 mg once in a day.

Same symptoms don't mean you have the same problem. Consult a doctor now!

Dr. Babu Lal Meena
Dr. Babu Lal Meena

Medical Gastroenterology

Community Banner Mobile
By subscribing, I agree to iCliniq's Terms & Privacy Policy.

Ask your health query to a doctor online

Medical Gastroenterology

*guaranteed answer within 4 hours

Disclaimer: No content published on this website is intended to be a substitute for professional medical diagnosis, advice or treatment by a trained physician. Seek advice from your physician or other qualified healthcare providers with questions you may have regarding your symptoms and medical condition for a complete medical diagnosis. Do not delay or disregard seeking professional medical advice because of something you have read on this website. Read our Editorial Process to know how we create content for health articles and queries.

This website uses cookies to ensure you get the best experience on our website. iCliniq privacy policy