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. 2026 Apr 1;14:1776405. doi: 10.3389/fpubh.2026.1776405

Table 3.

Risk of bias and quality assessment of included studies using the Newcastle–Ottawa Scale (NOS).

Study Study design Selection (max 4) Comparability (max 2) Exposure/ Outcome (max 3) Total Score/9 Quality rating
Kim et al. (22) Case–control ★★★★ ★★ ★★ 8 Low risk (good quality); validated GC–MS exposure ascertainment
Durmaz et al. (23) Case–control ★★★★ ★★ ★★ 8 Low risk (good quality); creatinine-adjusted BPA measurement
Lee et al. (24) Cross-sectional ★★ ★★ ★★ 6 Moderate risk; cross-sectional exposure–outcome assessment limits temporality
Supornsilchai et al. (25) Case–control ★★★★ ★★ ★★ 8 Low risk (good quality); high-sensitivity LC–MS/MS method
Jung et al. (26) Case–control ★★★★ ★★ ★★ 8 Low risk (good quality); multicenter recruitment
Chen et al. (27) Case–control ★★★★ ★★ ★★ 8 Low risk (good quality); matched design and internal QC
Mohsen et al. (28) Cross-sectional ★★ ★★ ★★ 6 Moderate risk; limited adjustment for confounders
Durmaz et al. (29) Case–control ★★★★ ★★ ★★ 8 Low risk (good quality); clinically well-defined PT cases
Vu Huynh et al. (30) Case–control ★★★★ ★★ ★★ 8 Low risk (good quality); large sample size and recent data

★ indicates a point awarded for meeting a specific NOS criterion. NOS, Newcastle–Ottawa Scale; HPLC, high-performance liquid chromatography; LC–MS/MS, liquid chromatography–tandem mass spectrometry; UPLC–MS/MS, ultra-performance liquid chromatography–tandem mass spectrometry; GC–MS, gas chromatography–mass spectrometry; CPP, central precocious puberty; BMI, body mass index.