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Complete Blood Count (CBC) Test Overview

Published: August 9, 2026Updated: August 16, 2026

This test measures the level of 1-methylhistidine, a byproduct of muscle metabolism, in the amniotic fluid surrounding the baby during pregnancy.

Quick summary

{"1-Methylhistidine is a natural chemical produced when the body breaks down certain proteins","This test helps doctors evaluate fetal development and detect potential metabolic disorders","The test is performed on a sample of amniotic fluid collected during pregnancy","Abnormal levels may indicate issues with fetal muscle metabolism or genetic conditions"}

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
27162-7
Short code
1Me-hist Amn-sCnc
Synonyms
1Me-hist Amn-sCnc
Category
chemistry
Sample
fluid
Container
Sterile tube
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Specimen volume
2-5 mL
Stability
Room temperature: 2h, Refrigerated: 24h
Hemolysis max
300
TAT
4–24 hours
Order
routine

The complete blood count (CBC) is a common blood test that measures the different cells in your blood, including red blood cells, white blood cells, and platelets, and helps your doctor evaluate your overall health and screen for many conditions.

The 1-methylhistidine test measures the amount of 1-methylhistidine in amniotic fluid. 1-Methylhistidine is a compound produced when the body metabolizes certain amino acids, particularly from muscle tissue. This test is part of prenatal screening that helps healthcare providers assess fetal health and development.

A healthcare professional will draw a small sample of blood from a vein in your arm, usually on the inside of your elbow, using a thin needle. The procedure takes only a few minutes, and you can return to your normal activities right afterward.

During amniocentesis, a healthcare provider uses ultrasound guidance to insert a thin needle through the abdomen and into the uterus to collect a small sample of amniotic fluid. The sample is then sent to a laboratory where the level of 1-methylhistidine is measured. This procedure is typically performed between 15-20 weeks of pregnancy, though timing may vary based on clinical needs.

This test is important because it helps detect a wide range of conditions, such as anemia, infections, and blood disorders, often before symptoms appear, allowing your doctor to diagnose problems early and plan the most appropriate treatment for you.

Measuring 1-methylhistidine in amniotic fluid can provide important information about fetal metabolism. Abnormal levels may suggest certain genetic metabolic disorders or issues with fetal muscle development. This information helps healthcare providers make informed decisions about pregnancy management and prepare for any necessary interventions after birth.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

The 1-methylhistidine test helps detect potential metabolic disorders in the fetus, including certain amino acid metabolism abnormalities. Elevated or reduced levels may indicate conditions affecting muscle metabolism or genetic disorders. This test is often used in conjunction with other prenatal tests to provide a comprehensive assessment of fetal health. Results help healthcare providers determine if additional testing or special care is needed during pregnancy and after delivery.

Frequently asked questions

Is this test safe for my baby?
Amniocentesis carries a small risk of complications, including infection, bleeding, or miscarriage. The procedure is performed under ultrasound guidance to minimize risks. Your healthcare provider will discuss the risks and benefits with you before the test.
How long does it take to get results?
Results typically take several days to a week, as the sample requires specialized laboratory analysis. Your healthcare provider will contact you with results and explain what they mean for your pregnancy.
What do abnormal results mean?
Abnormal 1-methylhistidine levels may indicate a metabolic disorder or genetic condition. However, further testing is usually needed to confirm a diagnosis. Your healthcare provider will explain the results and recommend appropriate follow-up care.
Does an abnormal result mean my baby will have health problems?
Not necessarily. Abnormal results require further investigation to determine the cause. Some abnormalities may be temporary or have minimal impact, while others may require special planning for delivery and newborn care. Your healthcare team will provide guidance and support.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy