Romano Elena, Rinzivillo Maria, Lamberti Giuseppe, Marasco Matteo, Esposito Gianluca, Campana Davide, Panzuto Francesco
Digestive Disease Unit, Department of Medical-Surgical Sciences and Translational Medicine, Sant'Andrea University Hospital, Sapienza University of Rome, ENETS Center of Excellence, Rome, Italy.
Department of Medical and Surgical Sciences (DIMEC), Alma Mater Studiorum-University of Bologna, Medical Oncology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Transl Gastroenterol Hepatol. 2025 May 29;10:57. doi: 10.21037/tgh-24-113. eCollection 2025.
Chromogranin A (CgA) is extensively recognized as a biomarker in neuroendocrine neoplasms (NENs) due to its secretion alongside peptide hormones and biogenic amines in neuroendocrine cells. Despite its widespread clinical use, the reliability of CgA as a diagnostic and prognostic tool remains controversial because of its variable expression in various diseases and the influence of factors such as medication and disease characteristics. This review critically examines the role of CgA beyond neuroendocrine contexts, particularly in gastrointestinal conditions where increased levels may mislead clinical diagnostics.
This review was conducted by performing a search on the PubMed database regarding CgA and both pathological and non-pathological conditions, excluding NENs.
Conditions such as chronic atrophic gastritis (CAG), proton pump inhibitor usage, and inflammatory bowel diseases (IBDs), among others, can lead to elevated CgA levels, often without any malignant association. Studies reviewed underscore the necessity for cautious interpretation of elevated CgA levels to avoid misdiagnosis and unnecessary anxiety in patients. The review further discusses the implications of non-neuroendocrine diseases contributing to elevated CgA levels, emphasizing the need for improved specificity in testing and a greater awareness among clinicians about the factors influencing CgA levels.
This comprehensive understanding assists in better managing patient outcomes through more accurate diagnosis and appropriate therapeutic interventions.
嗜铬粒蛋白A(CgA)在神经内分泌细胞中与肽类激素和生物胺一同分泌,因此被广泛认为是神经内分泌肿瘤(NENs)的生物标志物。尽管其在临床中广泛应用,但由于其在各种疾病中的表达存在差异以及药物和疾病特征等因素的影响,CgA作为诊断和预后工具的可靠性仍存在争议。本综述批判性地研究了CgA在神经内分泌背景之外的作用,特别是在胃肠道疾病中,其水平升高可能会误导临床诊断。
通过在PubMed数据库中搜索关于CgA以及除NENs之外的病理和非病理状况来进行本综述。
慢性萎缩性胃炎(CAG)、质子泵抑制剂的使用以及炎症性肠病(IBDs)等状况可导致CgA水平升高,且通常与恶性情况无关。所综述的研究强调谨慎解读CgA水平升高的必要性,以避免对患者的误诊和不必要的焦虑。该综述进一步讨论了非神经内分泌疾病导致CgA水平升高的影响,强调检测需提高特异性以及临床医生需更清楚了解影响CgA水平的因素。
这种全面的认识有助于通过更准确的诊断和适当的治疗干预更好地管理患者的预后。