Journal of Clinical Pharmacy and Therapeutics最新文献

{"title":"Efficacy of Biological or Targeted Synthetic Disease-Modifying Anti-Rheumatic Drugs in Active Psoriatic Arthritis: A Network Meta-Analysis of Randomized Controlled Trials","authors":"Siming Gao,&nbsp;Hui Song","doi":"10.1155/jcpt/6541156","DOIUrl":"https://doi.org/10.1155/jcpt/6541156","url":null,"abstract":"<div>\u0000 <p><b>Objective:</b> Many biological or targeted synthetic disease-modifying anti-rheumatic drugs (b/ts DMARDs) are used in the treatment of psoriatic arthritis (PsA) during recent years, but there are few head-to-head studies that directly compare these drugs to evaluate and compare the relative efficacy of these treatments at week 24. The aim of this study is to conduct a comprehensive comparison of all clinically used bDMARDs or tsDMARDs for PSA using a network meta-analysis to evaluate relative efficacy of these drugs, which is evaluated by ACR20, ACR50, ACR70, PASI75, and PASI90.</p>\u0000 <p><b>Methods:</b> All randomized controlled trials of these treatments are searched in PubMed, Web of Science, and Embase, and data are extracted from the included articles, and network meta-analysis is performed using the Stata 13 software.</p>\u0000 <p><b>Results:</b> secukinumab 300 mg is the top-ranked treatment for ACR20 and PASI90, infliximab 5 mg/kg is the top-ranked treatment for ACR50, and adalimumab 40 mg is the top-ranked treatment for ACR70 and PASI75.</p>\u0000 <p><b>Conclusions:</b> Tumor necrosis factor-α inhibitors and interleukin 17A inhibitors are the top-ranked treatments for arthritis and skin responses of active PsA.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/6541156","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143717223","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Exploring the Therapeutic Effect of Quercetin in Asthma and Pulmonary Fibrosis Overlap Syndrome Post-COVID-19","authors":"Baolan Wang,&nbsp;Zhe Zhang,&nbsp;Yi Wang,&nbsp;Rong Zhu,&nbsp;Xiuqin Zhang","doi":"10.1155/jcpt/5548573","DOIUrl":"https://doi.org/10.1155/jcpt/5548573","url":null,"abstract":"<div>\u0000 <p><b>Backgrounds:</b> Quercetin has potentially beneficial therapeutic effects for several chronic, inflammatory disorders of the airways. Thus, we explore the therapeutic value and mechanism of quercetin in the treatment of asthma and pulmonary fibrosis overlap syndrome after COVID-19.</p>\u0000 <p><b>Methods:</b> The potential targets and molecular mechanisms of quercetin for the treatment of overlap syndrome were predicted using a network pharmacology method. The binding mechanism between the core potential compounds and their targets was predicted using molecular docking with AutoDock Vina. An asthma model induced by ovalbumin was built to evaluate the effect of quercetin on asthma.</p>\u0000 <p><b>Results:</b> 55 common targets and eight key genes between the overlap syndrome and quercetin were obtained for further study. Most of the interested target genes were mainly focused on inflammation-related signaling pathways. Via molecular docking, quercetin showed a high degree of affinity for TNF, IL-6, and MMP9. In addition, quercetin improved asthma symptoms, inflammatory response, and pulmonary fibrosis.</p>\u0000 <p><b>Conclusion:</b> This study, which examined the use of quercetin for the treatment of the overlap syndrome of asthma and pulmonary fibrosis following COVID-19 from the aspect of network pharmacology, might serve as a useful guidepost for future studies and clinical applications.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/5548573","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143717374","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A Network Pharmacology-Based Strategy for Predicting Anti-Inflammatory Targets of Zao Ren An Shen Capsule in the Treatment of Asthma","authors":"Baolan Wang,&nbsp;Zhe Zhang,&nbsp;Yi Wang,&nbsp;Rong Zhu,&nbsp;Xiuqin Zhang","doi":"10.1155/jcpt/4669223","DOIUrl":"https://doi.org/10.1155/jcpt/4669223","url":null,"abstract":"<div>\u0000 <p><b>Backgrounds:</b> The Zao Ren An Shen (ZRAS) Capsule, stemming from a traditional Chinese herbal formula, is recognized as a safe and effective sleep-regulating medication. Asthma often worsens during the night and early morning due to its distinct day–night rhythm, suggesting the potential for the ZRAS Capsule to intervene in asthma attacks and prognosis. Since inflammation is a primary mechanism in asthma, exploring the anti-inflammatory effects of the ZRAS Capsule is essential.</p>\u0000 <p><b>Methods:</b> This study identifies the intersection of ZRAS Capsule-related targets and anti-inflammatory targets to uncover potential anti-inflammatory mechanisms. Core compounds and relevant genes were identified using protein–protein and compound–protein interaction networks. KEGG pathway and Gene Ontology analyses were performed on the anti-inflammatory targets to validate their role in mitigating asthma inflammation. Binding activities between the compounds and anti-inflammatory targets were assessed using western blot, qRT-PCR, molecular docking, and immunohistochemistry (IHC).</p>\u0000 <p><b>Results:</b> Key compounds, including luteolin, (S)-Coclaurine, and zizyphusine, along with targets IL6, TNF, and MMP9, were identified. Their biological processes were linked to the IL-17 signaling pathway and TNF signaling pathway. Notably, the identified compounds inhibited the mRNA and protein expression of IL6, TNF, and MMP9.</p>\u0000 <p><b>Conclusion:</b> Regulation of the IL-17/TNF signaling pathway is likely crucial for the protective effects of the ZRAS Capsule in asthma treatment.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/4669223","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143707537","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Pirfenidone Alleviates Intrauterine Infection-Induced Lung Injuries in Neonates by Targeting Transforming Growth Factor Beta 1/Sma- and Mad-Related Protein Signaling Pathway","authors":"Wenling Ding,&nbsp;Renchang Liu,&nbsp;Chunyou Wu,&nbsp;Ruobing Shan","doi":"10.1155/jcpt/6656368","DOIUrl":"https://doi.org/10.1155/jcpt/6656368","url":null,"abstract":"<div>\u0000 <p><b>Objective:</b> To explore the effect and mechanism of pirfenidone (PFD) on lung injuries in newborn rats caused by intrauterine inflammation.</p>\u0000 <p><b>Methods:</b> In vivo, we established the intrauterine inflammation model with lipopolysaccharide (LPS) injection in pregnant rats. The administration of PFD in pregnant rats was performed to evaluate its beneficial effect against intrauterine inflammation-induced lung injuries in neonatal rats. Lung tissues of newborns from three groups of pregnant rats (Saline + DMSO, LPS + DMSO, and LPS + PFD) were collected. Immunohistochemistry (IHC) and Western blot were used to detect the fibrotic-related protein expressions. In vitro, LPS-induced mouse lung epithelial cells (MLE 12) were employed to explore the underlying mechanism of PFD against intrauterine inflammation-induced lung injury in neonates.</p>\u0000 <p><b>Results:</b> In vivo, the radial alveolar count (RAC) was decreased, the mean linear intercept (MLI) was increased, and the lung injury score was high in intrauterine inflammation (LPS + DMSO-treated pregnant rats) induced lung injuries in newborns. The protein level of matrix metallopeptidase 9 (MMP-9), TGF-β1 (transforming growth factor beta 1), phospho-Smad2 (Sma- and mad-related protein 2), and phosphor-Smad3 (Sma- and mad-related protein 3) levels were upregulated in neonatal lungs with intrauterine infection. Lung injuries were alleviated in LPS + PFD groups, and the protein levels of TGF-β1, p-Smad2, p-Smad3, and MMP-9 were reduced. In vitro, PFD attenuated the LPS-induced inflammatory response and reduced the expressions of MMP-9, TIMP-1, and Collagen IV in lung epithelial cells through the TGF-β1/Smad2/3 signaling pathway.</p>\u0000 <p><b>Conclusions:</b> PFD alleviates intrauterine infection-induced lung injuries in neonates by targeting transforming growth factor beta 1/Sma- and mad-related protein signaling pathway. The inhibition of TGF-β1 signaling by PFD prevents the neonatal lung injuries by reducing MMP-9 and Collagen IV protein levels. This study provides theoretical basis and insights for PFD-mediated intervention of lung injury in neonates with intrauterine infection.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/6656368","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143707536","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Exploring the Antibiofilm and Antibacterial Potential of Datura stramonium and Prosopis farcta Against Gram-Positive and Gram-Negative Bacteria","authors":"Soheila Shahroodian,&nbsp;Maryam Mirshekar,&nbsp;Maryam Koupaei,&nbsp;Shiva Mirkalantari,&nbsp;Nour Amirmozafari","doi":"10.1155/jcpt/4815952","DOIUrl":"https://doi.org/10.1155/jcpt/4815952","url":null,"abstract":"<div>\u0000 <p><b>Background</b>: The rise of drug-resistant bacteria poses a significant challenge to global healthcare, underscoring the urgent need for new therapeutic interventions. In this study, ethanolic extracts of <i>Datura stramonium</i> and <i>Prosopis farcta</i>, sourced from Northern Iran, were examined for their antibacterial properties against <i>Staphylococcus aureus</i>, <i>Escherichia coli</i>, <i>Acinetobacter baumannii</i>, <i>Klebsiella pneumoniae</i>, and <i>Pseudomonas aeruginosa</i>.</p>\u0000 <p><b>Methods:</b> The antibacterial activities of the medicinal extracts were examined in this study using disc diffusion, microbroth dilution, and agar well diffusion methods against both Gram-positive and Gram-negative microorganisms. In addition, the extracts were assessed for toxicity using the MTT assay on HT29 cells. The biofilm-inhibitory effects of the extracts were also investigated.</p>\u0000 <p><b>Results:</b> The results showed that the ethanolic extracts from <i>D. stramonium</i> and <i>P. farcta</i> have strong antibacterial activity against <i>S. aureus</i>. However, their activity against <i>P. aeruginosa</i> and <i>A. baumannii</i> is less pronounced. The extracts showed significant antibiofilm capabilities against the tested bacteria at both MIC and 2× MIC concentrations (<i>p</i> &lt; 0.05). The MTT test showed HT29 cells were more sensitive to <i>P. farcta</i> extract than <i>D. stramonium,</i> especially at 200 μg/mL concentration.</p>\u0000 <p><b>Conclusion:</b> The findings demonstrate that ethanolic extracts of <i>P. farcta</i> and <i>D. stramonium</i> exhibit significant antibacterial activity, particularly against <i>S. aureus</i>, while also effectively disrupting bacterial biofilms. These results suggest that these extracts possess considerable potential as alternative therapeutic agents against drug-resistant bacterial infections. Further investigation is warranted to elucidate the specific mechanisms of action and to explore their efficacy in clinical applications.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/4815952","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143698902","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Efficacy and Safety of Intranasal Dexmedetomidine Combined With Oral Chloral Hydrate for Sedation in Neonatal MRI Procedures: A Single-Center Retrospective Study","authors":"Wenyan Dong,&nbsp;Lingdi Zhu,&nbsp;Linlin Xu,&nbsp;Zhenkun Yang,&nbsp;Shuoxiong Wu","doi":"10.1155/jcpt/6597033","DOIUrl":"https://doi.org/10.1155/jcpt/6597033","url":null,"abstract":"<div>\u0000 <p><b>Background:</b> Pharmacological sedation during neonatal magnetic resonance imaging (MRI) is crucial for procedure success and minimizing artifacts. Hence, it is vital to evaluate the effectiveness and safety of conventional sedatives in this population. In this study, we aim to evaluate the effectiveness of oral chloral hydrate combined with intranasal dexmedetomidine in neonatal MRI.</p>\u0000 <p><b>Methods:</b> Neonates aged 0 to 28 days undergoing MRI were enrolled and received intranasal dexmedetomidine followed by oral chloral hydrate. Subsequently, sedation scores, onset time, and overall time of sedation, as well as any potential adverse reactions, were recorded.</p>\u0000 <p><b>Results:</b> All neonates completed the MRI without notable adverse reactions. 128 neonates (90.1%) completed the MRI study with a single dose, while 14 neonates (9.9%) required additional medications. In the neonates with a single dose, no statistically significant differences in onset time were observed across postnatal days, gender, and weight. And no statistically significant differences in total time were observed across postnatal days and gender. However, the total time was significantly extended in the neonates with a weight under 3 kg. Furthermore, compared to the neonates with a single dose, the total time was significantly extended in the neonates with additional medications.</p>\u0000 <p><b>Conclusion:</b> Oral chloral hydrate combined with intranasal dexmedetomidine is effective and safe for neonatal MRI, but extra attention is needed for neonates under 3 kg.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/6597033","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143689939","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Impaired Autophagic Flux by Citalopram Inhibits DR5 Degradation and Increases TRAIL-Mediated Apoptosis","authors":"K. M. A. Zinnah,&nbsp;Ali Newaz Munna,&nbsp;Jae-Won Seol,&nbsp;Sang-Youel Park","doi":"10.1155/jcpt/7538839","DOIUrl":"https://doi.org/10.1155/jcpt/7538839","url":null,"abstract":"<div>\u0000 <p>To overcome TRAIL resistance, we tested the antidepressant drug citalopram (CTL) in combination with TRAIL. The resistance of several types of cancer cells to TRAIL impedes TRAIL-induced cancer cell death. In this study, we investigated the role of, and molecular mechanism by which, the antidepressant CTL-induced cell death in TRAIL-resistant lung cancer cells. We found that CTL increased death receptor 5 (DR5) expression levels by impairing autophagic flux and protecting against lysosomal degradation, thereby increasing the TRAIL-induced apoptosis of TRAIL-resistant A549 lung cancer cells. We also found that CTL impaired autophagic flux and promoted the conversion of light chain 3 (LC3)-I to its lipid-conjugated form, LC3-II, thereby inducing autophagosome accumulation. Our hypothesis that impaired autophagic flux plays an important role in the upregulation of DR5 being confirmed when we determined that DR5 upregulation by CTL was markedly decreased in the presence of rapamycin, an autophagy inducer. Further verification of our theory was achieved through experiments pairing CTL with the early-stage autophagy inhibitor 3-methyladenine (3-MA) and the late-stage autophagy inhibitor chloroquine (CQ). CQ inhibits autophagy by impairing autophagosome–lysosome fusion. Both CTL and CQ markedly increased DR5 expression levels and increase TRAIL-induced apoptosis, whereas 3-MA marginally enhanced TRAIL-induced apoptosis and resulted in minimal DR5 expression. In summary, our findings indicate that CTL impairs autophagic flux, resulting in autophagosome accumulation and augmentation of DR5 to potentiate TRAIL-induced apoptosis, suggesting that CTL may act as a therapeutic agent that sensitizes TRAIL-resistant cancer cells to TRAIL-mediated cancer therapy.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/7538839","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143689318","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"SGLT2 Inhibitors Increase Hemoglobin and Hematocrit Levels in Patients With Chronic Kidney Disease: A Systematic Review and Meta-Analysis","authors":"Hye Duck Choi,&nbsp;Seung Woo Lee","doi":"10.1155/jcpt/4354892","DOIUrl":"https://doi.org/10.1155/jcpt/4354892","url":null,"abstract":"<div>\u0000 <p><b>What Is Known and Objective:</b> Sodium-glucose cotransporter 2 (SGLT2) inhibitors improve renal and cardiovascular outcomes and have been reported to have a positive impact on anemia, a common and challenging condition in patients with chronic kidney disease (CKD). The aim of this study is to evaluate the effects of SGLT2 inhibitors on anemia in patients with CKD.</p>\u0000 <p><b>Methods:</b> We performed a systematic review and meta-analysis of randomized controlled trials. Changes in hemoglobin (Hb) and hematocrit (Hct) levels were assessed in participants treated with SGLT2 inhibitors—empagliflozin, dapagliflozin, or canagliflozin—and compared with those receiving control treatments. Statistical analyses were performed using a fixed-effects model or a random-effects model, depending on the heterogeneity. Sensitivity analyses were also conducted to evaluate the impact of each study on the meta-analysis. Publication bias was examined using Begg’s and Egger’s tests.</p>\u0000 <p><b>Results and Discussion:</b> Five studies assessing Hb levels were included. SGLT2 inhibitors significantly increased Hb levels compared with controls (standard difference in means [SE] = −0.350; 95% confidence interval [CI] −0.401–−0.299). Similarly, in three studies evaluating Hct levels, SGLT2 inhibitors significantly increased Hct levels compared with controls (SE = −0.453; 95% CI −0.829–0.077).</p>\u0000 <p><b>What Is New and the Conclusions:</b> This systematic review confirms that SGLT2 inhibitors effectively improve anemia in patients with CKD. We recommend considering SGLT2 inhibitors as a treatment option for CKD patients, not only for their renal and cardiovascular benefits but also for their reliability in addressing anemia.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/4354892","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143646324","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Population Pharmacokinetics and AUC-Based Dose Optimization of Vancomycin in Chinese Neonates","authors":"Caiyan Yang,&nbsp;Shifeng Wei,&nbsp;Bo Wang,&nbsp;Jiayu Yang,&nbsp;Zhigang Zhao,&nbsp;Daqing Xu,&nbsp;Shenghui Mei","doi":"10.1155/jcpt/6935260","DOIUrl":"https://doi.org/10.1155/jcpt/6935260","url":null,"abstract":"<div>\u0000 <p><b>Objective:</b> The primary objective of this study revolves around the development of a population pharmacokinetic (PPK) model for vancomycin in neonatal subjects, with the objective of providing a theoretical basis for judicious therapeutic interventions.</p>\u0000 <p><b>Methods:</b> In this study, a retrospective collection encompassed 75 neonatal patients, contributing to a total of 89 vancomycin blood concentration monitoring datasets. The establishment of the PPK model is carried out utilizing the nonlinear mixed effects model methodology. The PPK model was constructed employing a one-compartment model with proportional residual error, and the influence of covariates on pharmacokinetic parameters was systematically assessed through forward stepwise addition and backward elimination methods. The stability and predictive accuracy of the final model were assessed using goodness-of-fit plots, nonparametric bootstrap validation, visual predictive checks, and normalized prediction distribution errors. Furthermore, Monte Carlo simulations were employed to predict vancomycin concentrations in neonatal patients with typical characteristics.</p>\u0000 <p><b>Results:</b> The final PPK model yielded population-typical values of 0.24 L/h for vancomycin clearance (CL). Noteworthy contributors to vancomycin CL were identified as body weight, gestational age, creatinine clearance rate (CLcr), and sex. Internal validation results of the model indicate that it possesses stability, efficacy, and demonstrates a favorable predictive capacity. Monte Carlo simulations indicate that for a male neonatal patient characterized by a gestational age of 37 weeks, a body weight of 2.5 kg, and a CLcr of 60 mL/min, the recommended dosing regimen is 25.5 to 41.5 mg every 8 h.</p>\u0000 <p><b>Conclusion:</b> This investigation has successfully formulated a PPK model for vancomycin in neonatal patients, offering the capacity to estimate individual CL. The dosing regimen for neonates should take into account factors such as body weight, gestational age, CLcr, and sex.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/6935260","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143602549","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Proton Pump Inhibitor Use and Its Association With Asthma: A Systematic Review and Meta-Analysis","authors":"Ganesh Bushi,&nbsp;Mahalaqua Nazli Khatib,&nbsp;Suhas Ballal,&nbsp;Pooja Bansal,&nbsp;Balvir S. Tomar,&nbsp;Ayash Ashraf,&nbsp;M. Ravi Kumar,&nbsp;Aashna Sinha,&nbsp;Pramod Rawat,&nbsp;Abhay M. Gaidhane,&nbsp;Sanjit Sah,&nbsp;Hashem Abu Serhan,&nbsp;Mahendra Pratap Singh,&nbsp;Muhammed Shabil","doi":"10.1155/jcpt/6643853","DOIUrl":"https://doi.org/10.1155/jcpt/6643853","url":null,"abstract":"<div>\u0000 <p><b>Background:</b> Asthma is a prevalent chronic respiratory condition marked by airway inflammation and hyperresponsiveness, significantly impacting quality of life. Emerging evidence suggests a potential association between proton pump inhibitor (PPI) use and an increased risk of asthma. This systematic review and meta-analysis assessed the relationship between PPI use and the development or exacerbation of asthma.</p>\u0000 <p><b>Methods:</b> A systematic search of PubMed, Web of Science, and Embase databases was conducted, covering studies published from the inception of the database to July 12, 2024. Observational studies examining the association between PPI use and asthma risk were included. Two reviewers independently extracted data using Nested Knowledge software, with study quality assessed via the Newcastle–Ottawa Scale. A random-effects meta-analysis was performed, pooling odds ratios (ORs) and hazard ratios (HRs) to assess the association, with heterogeneity evaluated via the <i>I</i>² statistic.</p>\u0000 <p><b>Results:</b> Fourteen studies, conducted between 2009 and 2024 and involving over 1.7 million participants, met the inclusion criteria. The pooled HR showed a 38% increased risk of asthma among PPI users compared to nonusers (HR, 1.38; 95% CI, 1.14–1.62). OR analysis indicated a 29% higher risk (OR, 1.29; 95% CI, 1.23–1.35). PPI users had an 81% higher risk compared to histamine H₂ receptor antagonist (H₂RA) users (HR, 1.81; 95% CI, 1.09–2.53), and asthma patients using PPIs were 61% more likely to experience exacerbations (OR, 1.61; 95% CI, 1.42–1.80).</p>\u0000 <p><b>Conclusion:</b> PPI use is associated with an increased risk of asthma. These findings underscore the need for cautious prescribing and further investigation into underlying mechanisms.</p>\u0000 </div>","PeriodicalId":15381,"journal":{"name":"Journal of Clinical Pharmacy and Therapeutics","volume":"2025 1","pages":""},"PeriodicalIF":2.1,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jcpt/6643853","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143595023","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}