Singh Lovely, Fiza Mustaqueem Syed, Singh Priyanka, Jaiswal Pooja, Mohd Taj, Alam Roshan, Gupta Ashutosh, Keshav Rohit
Department of Pathology, Integral Institute of Medical Sciences and Research, Lucknow, IND.
Department of Biochemistry, Integral Institute of Medical Sciences and Research, Lucknow, IND.
Cureus. 2025 Aug 16;17(8):e90229. doi: 10.7759/cureus.90229. eCollection 2025 Aug.
Gallbladder pathology encompasses a spectrum from benign inflammation to aggressive malignancies, with gallbladder cancer (GBC) being one of the most lethal gastrointestinal cancers. Emerging evidence suggests that metabolic dysregulation, particularly lipid abnormalities, may drive carcinogenesis. However, the relationship between serum lipid profiles and gallbladder lesion progression remains poorly characterized.
This study aimed to investigate serum lipid abnormalities across benign (n = 48), premalignant (n = 11), and malignant (n = 12) gallbladder lesions to identify potential metabolic biomarkers for early detection and risk stratification.
A cross-sectional study was conducted on 71 cholecystectomy specimens (benign, premalignant, malignant) from April 2023 to March 2025. Histopathological evaluation categorized lesions, while fasting serum lipid profiles (total cholesterol, triglycerides, low-density lipoprotein (LDL), high-density lipoprotein (HDL), and very-low-density lipoprotein (VLDL)) were analyzed using automated biochemical assays. Statistical analysis included ANOVA and Pearson correlation tests, with significance at p < 0.05.
The cohort (mean age: 48.7 ± 14.1 years) showed female predominance (77.5%). Malignant lesions presented at older ages (mean: 55.1 years) and exhibited significant hypertriglyceridemia (301.75 ± 85.69 mg/dL; p = 0.014) and elevated VLDL (54.82 ± 22.74 mg/dL; p = 0.052) compared to benign/premalignant groups. HDL was the lowest in malignancies (37.00 ± 9.05 mg/dL).
Progressive lipid derangements - particularly hypertriglyceridemia, elevated VLDL, and reduced HDL - are associated with malignant transformation in gallbladder lesions. Serum lipid profiling may serve as a non-invasive tool for risk stratification and early detection. These findings highlight the potential for metabolic interventions in high-risk populations, though further longitudinal studies are needed to establish causality and therapeutic implications.
胆囊病理学涵盖了从良性炎症到侵袭性恶性肿瘤的一系列病变,胆囊癌(GBC)是最致命的胃肠道癌症之一。新出现的证据表明,代谢失调,尤其是脂质异常,可能驱动癌症发生。然而,血清脂质谱与胆囊病变进展之间的关系仍未得到充分描述。
本研究旨在调查良性(n = 48)、癌前(n = 11)和恶性(n = 12)胆囊病变中的血清脂质异常情况,以确定用于早期检测和风险分层的潜在代谢生物标志物。
对2023年4月至2025年3月期间的71例胆囊切除术标本(良性、癌前、恶性)进行了横断面研究。通过组织病理学评估对病变进行分类,同时使用自动生化分析法分析空腹血清脂质谱(总胆固醇、甘油三酯、低密度脂蛋白(LDL)、高密度脂蛋白(HDL)和极低密度脂蛋白(VLDL))。统计分析包括方差分析和Pearson相关性检验,p < 0.05具有统计学意义。
该队列(平均年龄:48.7 ± 14.1岁)以女性为主(77.5%)。恶性病变患者年龄较大(平均:55.1岁),与良性/癌前组相比,表现出显著的高甘油三酯血症(301.75 ± 85.