Diagnostic value of serum GDF-15 in patients with pseudomyxoma peritonei

Bing Wang1, Jie Zhang1, Ruiqing Ma2

  • 1Department of Clinical Laboratory of Aerospace Center Hospital, Beijing 100049, China.

Clinical Biochemistry
|September 20, 2024
PubMed
Abstract

Insights

Serum growth differentiation factor 15 (GDF-15) shows promise as a diagnostic marker for pseudomyxoma peritonei (PMP). Combining GDF-15 with carbohydrate antigen 125 (CA125) significantly improves diagnostic accuracy for PMP.

Area of Science:

  • Oncology
  • Biochemistry
  • Medical Diagnostics

Background:

  • Pseudomyxoma peritonei (PMP) is a rare malignancy with limited diagnostic biomarkers.
  • Accurate diagnosis of PMP is challenging due to the lack of sensitive and specific serum markers.
  • Novel serum markers are needed to improve PMP diagnosis and patient management.

Purpose of the Study:

  • To investigate the diagnostic utility of serum growth differentiation factor 15 (GDF-15) in patients with PMP.
  • To evaluate GDF-15 as a potential biomarker for PMP diagnosis.
  • To compare the diagnostic performance of GDF-15 alone and in combination with CA125.

Main Methods:

  • A 1:1 matched case-control study was conducted with 44 PMP patients and 44 healthy controls.
  • Serum GDF-15 concentrations were measured using ELISA.
  • Receiver operating characteristic (ROC) curve analysis was employed to assess diagnostic value.

Main Results:

  • Serum GDF-15 levels were significantly higher in PMP patients (median 1192.77 pg/mL) compared to controls (median 533.27 pg/mL) (P<0.001).
  • GDF-15 demonstrated good diagnostic performance for PMP with an AUC of 0.907, 93.18% sensitivity, and 77.27% specificity.
  • The combination of GDF-15 and CA125 yielded a larger AUC (P=0.027) with 86.36% sensitivity and 95.45% specificity.

Conclusions:

  • Serum GDF-15 presents potential as a novel diagnostic marker for PMP.
  • Combining GDF-15 with CA125 offers superior diagnostic performance for PMP compared to GDF-15 alone.
  • GDF-15 levels correlate with age, suggesting potential age-related variations in PMP patients.