{"title":"胸腔积液中的潜在生物标志物:ACE1、ACE2和KLK12水平","authors":"Serkan Sen, Ahmet Dumanli","doi":"10.1155/ijcp/4269986","DOIUrl":null,"url":null,"abstract":"<div>\n <p><b>Aim:</b> This study aims to investigate the potential roles of angiotensin converting enzyme (ACE) 1 and ACE2, along with kallikrein-related peptidase 12 (KLK12) levels in pleural fluids and serum, in distinguishing between transudative and exudative pleural effusions.</p>\n <p><b>Methods:</b> Pleural fluid and serum samples were collected from a total of 46 patients. Levels of ACE1, ACE2, and KLK12 were measured using the ELISA method. Patients were classified as having transudative or exudative pleural effusions based on Light’s criteria. Data were analyzed using statistical methods.</p>\n <p><b>Results:</b> According to the study findings, ACE1 levels in pleural fluid were significantly higher in the exudative group compared with the transudative group. There was no significant difference observed in ACE2 levels between the two groups. Interestingly, KLK12 levels were found to be higher in the transudative group compared with the exudative group. In serum, both ACE1 and ACE2 levels were significantly higher in the exudative group.</p>\n <p><b>Discussion:</b> These results indicate that ACE1 and KLK12 may serve as important biomarkers in the diagnostic evaluation of pleural effusions. In particular, the pleural fluid to serum (PF/S) ratios of ACE1 and KLK12 showed statistically significant differences between transudative and exudative groups, highlighting their potential in differentiating pleural effusion etiologies. While pleural fluid ACE2 levels alone did not show a significant difference, serum ACE2 concentrations and PF/S ACE2 ratios differed significantly, suggesting possible systemic changes. These findings underscore the importance of evaluating serum parameters alongside pleural fluid analysis as such comparisons may enhance diagnostic accuracy. However, the relatively small sample size limits the generalizability of these results, and further studies with larger cohorts are warranted to confirm these findings.</p>\n </div>","PeriodicalId":13782,"journal":{"name":"International Journal of Clinical Practice","volume":"2025 1","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/ijcp/4269986","citationCount":"0","resultStr":"{\"title\":\"Potential Biomarkers in Pleural Effusions: ACE1, ACE2, and KLK12 Levels\",\"authors\":\"Serkan Sen, Ahmet Dumanli\",\"doi\":\"10.1155/ijcp/4269986\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n <p><b>Aim:</b> This study aims to investigate the potential roles of angiotensin converting enzyme (ACE) 1 and ACE2, along with kallikrein-related peptidase 12 (KLK12) levels in pleural fluids and serum, in distinguishing between transudative and exudative pleural effusions.</p>\\n <p><b>Methods:</b> Pleural fluid and serum samples were collected from a total of 46 patients. Levels of ACE1, ACE2, and KLK12 were measured using the ELISA method. Patients were classified as having transudative or exudative pleural effusions based on Light’s criteria. Data were analyzed using statistical methods.</p>\\n <p><b>Results:</b> According to the study findings, ACE1 levels in pleural fluid were significantly higher in the exudative group compared with the transudative group. There was no significant difference observed in ACE2 levels between the two groups. Interestingly, KLK12 levels were found to be higher in the transudative group compared with the exudative group. In serum, both ACE1 and ACE2 levels were significantly higher in the exudative group.</p>\\n <p><b>Discussion:</b> These results indicate that ACE1 and KLK12 may serve as important biomarkers in the diagnostic evaluation of pleural effusions. In particular, the pleural fluid to serum (PF/S) ratios of ACE1 and KLK12 showed statistically significant differences between transudative and exudative groups, highlighting their potential in differentiating pleural effusion etiologies. While pleural fluid ACE2 levels alone did not show a significant difference, serum ACE2 concentrations and PF/S ACE2 ratios differed significantly, suggesting possible systemic changes. These findings underscore the importance of evaluating serum parameters alongside pleural fluid analysis as such comparisons may enhance diagnostic accuracy. However, the relatively small sample size limits the generalizability of these results, and further studies with larger cohorts are warranted to confirm these findings.</p>\\n </div>\",\"PeriodicalId\":13782,\"journal\":{\"name\":\"International Journal of Clinical Practice\",\"volume\":\"2025 1\",\"pages\":\"\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-07-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1155/ijcp/4269986\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Clinical Practice\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1155/ijcp/4269986\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Clinical Practice","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1155/ijcp/4269986","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
Potential Biomarkers in Pleural Effusions: ACE1, ACE2, and KLK12 Levels
Aim: This study aims to investigate the potential roles of angiotensin converting enzyme (ACE) 1 and ACE2, along with kallikrein-related peptidase 12 (KLK12) levels in pleural fluids and serum, in distinguishing between transudative and exudative pleural effusions.
Methods: Pleural fluid and serum samples were collected from a total of 46 patients. Levels of ACE1, ACE2, and KLK12 were measured using the ELISA method. Patients were classified as having transudative or exudative pleural effusions based on Light’s criteria. Data were analyzed using statistical methods.
Results: According to the study findings, ACE1 levels in pleural fluid were significantly higher in the exudative group compared with the transudative group. There was no significant difference observed in ACE2 levels between the two groups. Interestingly, KLK12 levels were found to be higher in the transudative group compared with the exudative group. In serum, both ACE1 and ACE2 levels were significantly higher in the exudative group.
Discussion: These results indicate that ACE1 and KLK12 may serve as important biomarkers in the diagnostic evaluation of pleural effusions. In particular, the pleural fluid to serum (PF/S) ratios of ACE1 and KLK12 showed statistically significant differences between transudative and exudative groups, highlighting their potential in differentiating pleural effusion etiologies. While pleural fluid ACE2 levels alone did not show a significant difference, serum ACE2 concentrations and PF/S ACE2 ratios differed significantly, suggesting possible systemic changes. These findings underscore the importance of evaluating serum parameters alongside pleural fluid analysis as such comparisons may enhance diagnostic accuracy. However, the relatively small sample size limits the generalizability of these results, and further studies with larger cohorts are warranted to confirm these findings.
期刊介绍:
IJCP is a general medical journal. IJCP gives special priority to work that has international appeal.
IJCP publishes:
Editorials. IJCP Editorials are commissioned. [Peer reviewed at the editor''s discretion]
Perspectives. Most IJCP Perspectives are commissioned. Example. [Peer reviewed at the editor''s discretion]
Study design and interpretation. Example. [Always peer reviewed]
Original data from clinical investigations. In particular: Primary research papers from RCTs, observational studies, epidemiological studies; pre-specified sub-analyses; pooled analyses. [Always peer reviewed]
Meta-analyses. [Always peer reviewed]
Systematic reviews. From October 2009, special priority will be given to systematic reviews. [Always peer reviewed]
Non-systematic/narrative reviews. From October 2009, reviews that are not systematic will be considered only if they include a discrete Methods section that must explicitly describe the authors'' approach. Special priority will, however, be given to systematic reviews. [Always peer reviewed]
''How to…'' papers. Example. [Always peer reviewed]
Consensus statements. [Always peer reviewed] Short reports. [Always peer reviewed]
Letters. [Peer reviewed at the editor''s discretion]
International scope
IJCP publishes work from investigators globally. Around 30% of IJCP articles list an author from the UK. Around 30% of IJCP articles list an author from the USA or Canada. Around 45% of IJCP articles list an author from a European country that is not the UK. Around 15% of articles published in IJCP list an author from a country in the Asia-Pacific region.