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Pregnancy-associated plasma protein A (PAPP-A)

SI UNITS (recommended)

CONVENTIONAL UNITS



(First-Trimester Marker for Chromosomal Abnormalities & Placental Function)

Synonyms

  • PAPP-A
  • Pregnancy-associated plasma protein A
  • PAPPA
  • Metalloproteinase PAPP-A
  • First-trimester Down syndrome marker
  • Placental protein A

Units of Measurement

  • mIU/L
  • µIU/mL
  • IU/L
  • mIU/mL

Unit Relationships

1 mIU/mL=1000 mIU/L1\ \text{mIU/mL} = 1000\ \text{mIU/L}1 mIU/mL=1000 mIU/L 1 µIU/mL=0.001 mIU/mL1\ \text{µIU/mL} = 0.001\ \text{mIU/mL}1 µIU/mL=0.001 mIU/mL 1 IU/L=1000 mIU/L1\ \text{IU/L} = 1000\ \text{mIU/L}1 IU/L=1000 mIU/L

Most laboratories report PAPP-A in mIU/L or mIU/mL.

Description

Pregnancy-Associated Plasma Protein A (PAPP-A) is a large zinc-binding metalloproteinase produced mainly by:

  • Syncytiotrophoblasts of the placenta
  • Decidual cells
  • Granulosa cells

PAPP-A plays a key role in placental development through cleavage of insulin-like growth factor–binding proteins (IGFBPs), especially IGFBP-4 → increasing free IGF, promoting:

  • Trophoblast invasion
  • Placental perfusion
  • Fetal growth

PAPP-A is a first-trimester maternal serum marker used in aneuploidy screening.

Physiological Role

  • Enhances IGF bioavailability
  • Regulates trophoblast proliferation
  • Supports placental and fetal development
  • Influences vascular remodeling of uteroplacental circulation

Low PAPP-A reflects early placental dysfunction.

Clinical Significance

LOW PAPP-A (Most Important Finding)

Strongly associated with:

1. Trisomy Risk

Used in first-trimester aneuploidy screening:

  • Down syndrome (Trisomy 21)low PAPP-A
  • Trisomy 18
  • Trisomy 13

Typically:

  • PAPP-A < 0.4 MoM → elevated aneuploidy risk
  • PAPP-A < 0.2 MoM → high risk

2. Placental Dysfunction

Low PAPP-A in 1st trimester is linked with:

  • Preeclampsia
  • Fetal growth restriction (FGR/IUGR)
  • Preterm birth
  • Stillbirth
  • Placental abruption

3. Adverse Pregnancy Outcomes

Lower PAPP-A = higher risk.

4. First-Trimester Screening Panels

Part of FMF algorithm with:

  • Nuchal translucency (NT)
  • Free β-hCG
  • Maternal age
  • Doppler resistance indices

HIGH PAPP-A

Usually benign and not clinically problematic.

Mild increase seen in:

  • Multiple gestation
  • Diabetic pregnancies
  • High placental volume

Not used clinically to diagnose disease.

Reference Intervals (Gestation-Dependent)

(Values vary widely by gestational age; interpreted as MoM - Multiples of Median)

Absolute PAPP-A Values (General Ranges)

Gestational AgeTypical PAPP-A (mIU/mL)
8–9 weeks0.5 – 2.0 mIU/mL
10–11 weeks1.0 – 4.0 mIU/mL
11–12 weeks2.0 – 6.0 mIU/mL
12–13 weeks3.0 – 10.0 mIU/mL

(Exact values vary by assay → MoM is used.)

MoM Interpretation

  • 1.0 MoM → expected median
  • <0.4 MoM → high risk (aneuploidy, placental disease)
  • >1.5 MoM → usually normal/benign

Diagnostic Uses

1. First-Trimester Combined Screening (Primary Use)

PAPP-A + NT + free β-hCG for detecting:

  • Down syndrome (T21)
  • Edwards syndrome (T18)
  • Patau syndrome (T13)

2. Predicting Placental Insufficiency

Low PAPP-A strongly linked with:

  • Early-onset preeclampsia
  • IUGR
  • Preterm birth
  • Stillbirth
  • Abnormal uterine artery Dopplers

3. Maternal-Fetal Risk Stratification

Women with PAPP-A <0.3 MoM often undergo:

  • Serial growth scans
  • Additional Doppler studies
  • Closer surveillance in 2nd–3rd trimester

4. First-Trimester Fetal Health Indicator

Reflects overall placental health early in pregnancy.

Analytical Notes

  • Sample: maternal serum
  • Best measured between 8–13+6 weeks
  • Strong gestational-age dependency → MUST convert to MoM
  • Hemolysis and lipemia may interfere with assays
  • Automated immunoassays used (chemiluminescence, ELISA)

Clinical Pearls

  • Low PAPP-A = placental dysfunction until proven otherwise.
  • When PAPP-A is low, always check uterine artery Doppler at 20–24 weeks.
  • Extreme low (<0.2 MoM) strongly predicts early severe preeclampsia.
  • PAPP-A is not a stand-alone test — used only as part of combined screening.
  • High PAPP-A values generally have no adverse clinical meaning.

Interesting Fact

PAPP-A was originally discovered as a protein elevated in pregnancy serum - later found to be a protease regulating IGF, crucial to placental development. Its molecular role explains why low levels indicate poor placental growth.

References

  1. Tietz Clinical Chemistry & Molecular Diagnostics, 8th Edition - Maternal Serum Screening
  2. Fetal Medicine Foundation (FMF) - PAPP-A Screening
  3. ACOG - First-Trimester Screening Guidelines
  4. ISUOG - Early Pregnancy Biomarkers
  5. Mayo Clinic Laboratories - PAPP-A
  6. ARUP Consult - Maternal Serum Screening
  7. NIH / MedlinePlus - PAPP-A Test

Last updated: January 27, 2026

Reviewed by : Medical Review Board

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