Key result
Lower serum ANGPTL8 identifies PCOS with an AUC of ~0.88.
Why the study?
The study was conducted to analyze the correlation between ANGPTL8 and PCOS and explore the clinical diagnostic value of ANGPTL8 in PCOS.
Does serum ANGPTL8 level correlate with PCOS and have clinical diagnostic value?
Case-Control (n=210)
No
Does serum ANGPTL8 level correlate with PCOS and have clinical diagnostic value?
Effect estimate: AUC 0.881 (95% CI 0.836-0.926)
p-value: p=<0.001
Serum ANGPTL8 levels are significantly lower in PCOS patients and show promise as a novel diagnostic biomarker, especially when combined with sex hormones.
May not support routine ANGPTL8 testing for PCOS; leaves open diagnostic utility pending prospective validation.
OBJECTIVE: To analyze the correlation between angiopoietin-like protein 8 (ANGPTL8) and polycystic ovary syndrome (PCOS) and explore the clinical diagnostic value of ANGPTL8 in PCOS. METHODS: In this retrospective case-control study, we included 94 PCOS patients (study group) from our hospital's Reproductive Center from June 2023 to December 2024 and 116 age-matched women with normal ovarian function (control group) from the Gynecology Department. Serum levels of anti-Müllerian hormone (AMH), sex hormones, and ANGPTL8 were measured in all participants. RESULTS: The study group exhibited higher AMH, LH, LH/FSH ratio, and E2 levels compared to the control group (p < 0.001). Serum ANGPTL8 levels were lower in PCOS patients (p < 0.001). Logistic multivariate regression analysis identified BMI, AMH, LH, and ANGPTL8 as independent influencing factors for PCOS. Elevated ANGPTL8 levels were associated with reduced PCOS risk (p < 0.001), while increased BMI, AMH, and LH levels correlated with higher PCOS risk (p < 0.05). At a cutoff value of 12.871 ng/mL, ANGPTL8 demonstrated a sensitivity of 90.4%, specificity of 77.6%, and an area under the curve (AUC) of 0.881 (95% CI: 0.836-0.926, p < 0.001), indicating moderate-to-high diagnostic efficacy. The combined use of ANGPTL8 with AMH or sex hormones improved diagnostic performance compared to individual markers. Notably, the combination of ANGPTL8 and sex hormones yielded a higher AUC (0.980) than ANGPTL8 with AMH (AUC = 0.928). CONCLUSION: Serum ANGPTL8 levels are significantly lower in PCOS patients and inversely associated with PCOS risk. ANGPTL8 shows promise as a novel diagnostic biomarker for PCOS, especially when integrated into multi-marker panels with existing hormonal parameters.
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Wang et al. (2026) conducted a case-control in Polycystic ovary syndrome (PCOS) (n=210). Serum ANGPTL8 levels vs. Normal ovarian function (controls) was evaluated on Diagnostic efficacy for PCOS (AUC 0.881, 95% CI 0.836-0.926, p=<0.001). Serum ANGPTL8 levels were significantly lower in PCOS patients and demonstrated diagnostic efficacy for PCOS at a cutoff of 12.871 ng/mL (AUC 0.881; 95% CI 0.836-0.926; P<0.001).
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