What are the C-Reactive Protein (CRP) levels during pregnancy?

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Last updated: March 14, 2025View editorial policy

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From the Guidelines

C-reactive protein (CRP) levels typically increase during normal pregnancy, with values often rising above the non-pregnant reference range, and can be measured as part of pregnancy registries in rheumatology, as recommended by the EULAR guidelines 1.

CRP Levels During Pregnancy

  • CRP levels may double from baseline during the first trimester, and by the third trimester, they can increase up to 5-fold, reaching values of 3-10 mg/L in uncomplicated pregnancies.
  • This physiological elevation occurs due to the inflammatory state associated with normal pregnancy as the maternal immune system adapts to accommodate the developing fetus.
  • Despite this normal increase, CRP remains a useful marker for detecting infections or inflammatory conditions during pregnancy, though interpretation requires consideration of these pregnancy-induced elevations.

Clinical Considerations

  • Significantly elevated CRP levels (typically >10 mg/L) may indicate infection, preeclampsia, or other pregnancy complications requiring further investigation.
  • Healthcare providers should use pregnancy-specific reference ranges when interpreting CRP values and consider the clinical context, gestational age, and other laboratory and clinical findings when evaluating pregnant patients with elevated CRP levels.
  • Regular monitoring may be necessary in high-risk pregnancies or when infection or inflammation is suspected, as part of a comprehensive approach to pregnancy care, including the assessment of other relevant factors, such as disease activity and patient-reported outcomes 1.

From the Research

C-Reactive Protein Levels During Pregnancy

  • C-Reactive Protein (CRP) levels during pregnancy have been studied to understand their role in diagnosing infections and predicting complications 2, 3, 4, 5, 6.
  • Median CRP values for women not in labor ranged from 0.7-0.9 mg/dL, depending on gestational age, with 95% of the values being 1.5 mg/dL or lower 2.
  • CRP values are higher in pregnant women than in non-pregnant individuals, with an upper reference limit of 19 mg/L in each trimester 3.
  • CRP levels increase linearly with body mass index (BMI) 3.
  • Elevated CRP levels during the first trimester of pregnancy may be indicative of preeclampsia and intrauterine growth restriction 5.
  • A cutoff value of >1.86 μg/mL for CRP has been found to be predictive of maternal adverse outcomes (MAO) 4.
  • CRP levels do not cross the placental barrier and may be useful in diagnosing infections in newborns 6.

Trimester-Specific Reference Intervals

  • Trimester-specific reference intervals for CRP have been defined, with an upper reference limit of 19 mg/L in each trimester 3.
  • Using pregnancy-specific reference intervals for CRP can improve diagnostic accuracy for infection 3.
  • CRP levels are similar in each trimester, with no consistent change in CRP levels with gestational age among serially sampled women not in labor 2.

Predictive Value of CRP

  • Elevated CRP levels at midpregnancy can predict gestational complications, including maternal and neonatal adverse outcomes 4.
  • CRP levels >1.86 μg/mL have been found to predict MAO, considering maternal age, hypertension, and gestational diabetes mellitus (GDM) 4.
  • Mean CRP levels were significantly elevated in women who later developed preeclampsia or delivered a growth-restricted baby 5.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

C-reactive protein in normal pregnancy.

Obstetrics and gynecology, 1991

Research

C-reactive protein during normal pregnancy.

European journal of obstetrics, gynecology, and reproductive biology, 1990

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.

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