We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
LGC Clinical Diagnostics

Ansh Labs

Develops and manufactures immunoassay reagent test kits used to advance target discovery, therapeutic development, bi... read more Featured Products: More products

Download Mobile App




Anti-Müllerian Hormone Immunoassay Validated

By LabMedica International staff writers
Posted on 04 Nov 2019
Print article
Image: The MenoCheck picoAMH ELISA is FDA cleared for in vitro diagnostic use as an aid in the determination of menopausal status in women between 42 and 62 years of age (Photo courtesy of Ansh Laboratories).
Image: The MenoCheck picoAMH ELISA is FDA cleared for in vitro diagnostic use as an aid in the determination of menopausal status in women between 42 and 62 years of age (Photo courtesy of Ansh Laboratories).
Anti-Müllerian hormone (AMH) is a homodimeric glycoprotein with roles in regulation of fetal sexual differentiation and folliculogenesis in the adult ovary. AMH is increasingly used as a biomarker of ovarian reserve in clinical practice, and is used both for management of fertility treatments and prediction of menopause.

The most common method of measurement used for AMH is enzyme-linked immunosorbent assay (ELISA), although earlier ELISA assays have suffered from problems with sample stability and measurement variability. Newer-generation assays have equivalent performance with fewer reproducibility issues.

A team of scientists from Baylor College of Medicine (Houston, TX, USA) collected 28 serum samples were collected from patients for whom AMH testing was requested and were measured by two assays. A subset of the specimens used in accuracy studies was used to perform correlation of AMH measurements with antral follicle count (AFC). Reference ranges given by the manufacturer were verified using samples from 26 healthy female volunteers aged 22–41 years with samples tested as previously described.

The team sought to validate the newly FDA-approved MenoCheck picoAMH ELISA (Ansh Laboratories, Webster, TX, USA) on the Dynex-DS2 platform (Dynex Technologies, Chantilly, VA, USA) for clinical use in their obstetrics and gynecology center. Accuracy of the picoAMH ELISA on the Dynex-DS2 was determined by comparison with ELISA performed onsite at the Ansh Laboratories’ CLIA-certified laboratory.

The investigators reported that Intra- and inter-assay CV of the picoAMH assay on the DS2 was ≤4% and the assay was linear between concentrations of 0.0067–16.24 ng/mL (0.048–116.0 pmol/L) AMH. Method comparison was performed with the manufacturer’s laboratory and indicated good correlation. The assay displayed no significant interference from hemolysis (1,000 mg/dL), lipemia (2,000 mg/dL), conjugated bilirubin (66 mg/dL), or biotin (10,000 ng/mL). Measurement of AMH on the DS2 was also correlated with antral follicle count, with R = 0.7128.

The authors concluded that their results indicate that the picoAMH ELISA on the DS2 has good analytical performance suitable for clinical use and that it can be used for patient testing in the reproductive endocrinology and infertility/in vitro fertilization (REI/IVF) setting in their hospital. The study was published in the November 2019 issue of the journal Practical Laboratory Medicine.

Related Links:
Baylor College of Medicine
Ansh Laboratories
Dynex Technologies


Gold Member
Fully Automated Cell Density/Viability Analyzer
BioProfile FAST CDV
New
Gold Member
Antipsychotic TDM Assays
Saladax Antipsychotic Assays
New
Basophil Activation Test
Flow CAST Kit
New
Mumps Virus Test
ReQuest Mumps IgG

Print article

Channels

Molecular Diagnostics

view channel
Image: A coronal MRI section shows a high-intensity focused ultrasound lesion in the left thalamus of the brain (Photo courtesy of UT Southwestern Medical Center)

Newly Identified Stroke Biomarkers Pave Way for Blood Tests to Quickly Diagnose Brain Injuries

Each year, nearly 800,000 individuals in the U.S. experience a stroke, which occurs when blood flow to specific areas of the brain is insufficient, causing brain cells to die due to a lack of oxygen.... Read more

Pathology

view channel
Image: As tumor cells flow through these microfluidic chambers, they are subjected to increasing shear stress and sorted based on their adhesion strength (Photo courtesy of UC San Diego)

Microfluidic Device Assesses Stickiness of Tumor Cells to Predict Cancer Spread

Ductal carcinoma in situ (DCIS), a type of early-stage breast cancer, is often referred to as stage zero breast cancer. In many cases, it remains harmless and does not spread beyond the milk ducts where... Read more
Copyright © 2000-2025 Globetech Media. All rights reserved.