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Search Results (1,700)

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10 pages, 1707 KiB  
Article
The Association Between Major Depression and Alzheimer’s Disease Risk: Evidence from a 12-Year Longitudinal Study
by Anais Sevil-Pérez, Raúl López-Antón, Patricia Gracia-García, Concepción de la Cámara, Ana Gascón-Catalán and Javier Santabárbara
J. Clin. Med. 2024, 13(23), 7039; https://doi.org/10.3390/jcm13237039 - 21 Nov 2024
Abstract
Background: The relationship between depression, particularly major depression (MD), as a risk factor for Alzheimer’s disease (AD) is well established; however, its precise role remains contested. Findings from the fourth wave of the ZARADEMP longitudinal study provide further insights into the association between [...] Read more.
Background: The relationship between depression, particularly major depression (MD), as a risk factor for Alzheimer’s disease (AD) is well established; however, its precise role remains contested. Findings from the fourth wave of the ZARADEMP longitudinal study provide further insights into the association between MD and AD risk. Objectives: This study aimed to examine the association between MD and incident AD, controlling for established risk factors. Methods: The study analyzed 4803 participants, of whom 4057 were followed over a 12-year period as part of the ZARADEMP longitudinal study. Depression was assessed using the GMS-AGECAT, and dementia was diagnosed according to DSM-IV criteria. The association between MD and incident AD was evaluated using Cox proportional hazards regression models. Results: The incidence of AD was approximately twice as high in participants with MD compared to those without (relative risk = 2.07; 95% CI: 0.85–5.03; p = 0.123). This risk was nearly threefold higher in the fully adjusted model. Conclusions: These findings underscore a significant association between MD and an increased risk of AD, emphasizing the need for vigilant monitoring and potential early intervention among individuals diagnosed with MD. Full article
(This article belongs to the Section Clinical Neurology)
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<p>Flowchart of study.</p>
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12 pages, 1487 KiB  
Article
Aortic Pulse Wave Velocity Determined with Oscillometric Pulse Wave Analysis Algorithm Antares Is an Independent Predictor of Major Adverse Cardiovascular Events: A Prospective Cohort Study
by Marcus Dörr, Harald Lapp, Stefan Richter, Alexander Stäuber, Martin Bahls, Stefan Gross, Marc-Alexander Ohlow, Siegfried Eckert, Franziska Stäuber, Matthias Wilhelm Hoppe and Johannes Baulmann
J. Clin. Med. 2024, 13(23), 7035; https://doi.org/10.3390/jcm13237035 - 21 Nov 2024
Abstract
Background/Objectives: Aortic pulse wave velocity (aPWV) is a well-established surrogate marker of arterial stiffness. The Antares algorithm offers a method for determining aPWV from oscillometric blood pressure waveforms without requiring additional inputs. This prospective study aimed to evaluate the association and prognostic [...] Read more.
Background/Objectives: Aortic pulse wave velocity (aPWV) is a well-established surrogate marker of arterial stiffness. The Antares algorithm offers a method for determining aPWV from oscillometric blood pressure waveforms without requiring additional inputs. This prospective study aimed to evaluate the association and prognostic value of aPWV, determined by Antares, in predicting major adverse cardiovascular events (MACE). Methods: In total, 240 patients (median age 69, 25.4% female) underwent oscillometric blood pressure measurements, from which aPWV was calculated using the Antares algorithm. MACE, comprising myocardial infarction, stroke, or all-cause mortality, occurred in 19.2% of patients during a median follow-up of 43 months. Survival analyses were performed using continuous aPWV values, a 10 m/s threshold, and aPWV quartiles. Kaplan–Meier curves and log-rank tests were used to compare survival across aPWV groups. Cox proportional hazards models were applied to assess the independent predictive value of aPWV. Results: Patients with aPWV < 10 m/s showed significantly higher event-free survival compared to those with aPWV ≥ 10 m/s (log-rank p = 0.044). Quartile analysis reinforced this, with the highest event rate in the highest aPWV quartile (log-rank p < 0.01). Multivariable analysis confirmed aPWV as an independent predictor of MACE (HR per 1 m/s: 1.24, 95% CI: 1.08–1.41; HR per 1 SD: 1.53, 95% CI: 1.17–2.00, p = 0.002). Adding aPWV to a risk model improved predictive accuracy (C-index 0.68 to 0.71). Conclusions: In the investigated cohort, aPWV derived using the Antares algorithm is an independent predictor of cardiovascular events. This non-invasive approach is promising for improving simple outpatient risk stratification and targeting preventive measures. Full article
(This article belongs to the Section Cardiovascular Medicine)
12 pages, 1684 KiB  
Article
Artificial Intelligence-Driven Volumetric Analysis of Muscle Mass as a Predictor of Tumor Response to Neoadjuvant Chemoradiotherapy in Patients with Rectal Cancer
by Minsung Kim, Sang Min Lee, Il Tae Son, Jaewoong Kang, Gyoung Tae Noh and Bo Young Oh
J. Clin. Med. 2024, 13(23), 7018; https://doi.org/10.3390/jcm13237018 - 21 Nov 2024
Viewed by 68
Abstract
Background/Objectives: Artificial intelligence (AI)-based volumetric measurements for assessing sarcopenia are expected to offer comprehensive insight into three-dimensional muscle volume and distribution. Therefore, we investigated the role of sarcopenia using computed tomography (CT)-based automated AI volumetric muscle measurements in predicting neoadjuvant chemoradiotherapy (nCRT) response [...] Read more.
Background/Objectives: Artificial intelligence (AI)-based volumetric measurements for assessing sarcopenia are expected to offer comprehensive insight into three-dimensional muscle volume and distribution. Therefore, we investigated the role of sarcopenia using computed tomography (CT)-based automated AI volumetric muscle measurements in predicting neoadjuvant chemoradiotherapy (nCRT) response and prognosis in patients with rectal cancer who underwent nCRT. Methods: We retrospectively analyzed the data of patients who underwent nCRT followed by curative resection between March 2010 and August 2021. Sarcopenia was defined using the Q1 cutoff value of the volumetric skeletal muscle index (SMI). The association between pre-nCRT volumetric sarcopenia and nCRT response was analyzed using logistic regression. A Cox proportional hazards model was used to identify the prognostic value of the pre- and post-nCRT volumetric SMIs. Results: Notably, 22 (25.6%) of the 86 patients had volumetric sarcopenia. The sarcopenia group showed a poorer nCRT response than the non-sarcopenia group. Pre-nCRT sarcopenia was a significant predictor of poor nCRT response (OR, 0.34 [95% CI, 0.12–0.96]; p = 0.041). Furthermore, an increased volumetric SMI during nCRT was a more significant prognostic factor on recurrence-free survival (aHR, 0.26 [95% CI, 0.08–0.83]; p = 0.023) and overall survival (aHR, 0.41 [95% CI, 0.17–0.99]; p = 0.049) than a decreased SMI. Conclusions: Volumetric sarcopenia can be used to predict poor nCRT response. A reduction in volumetric sarcopenia can be a poor prognostic factor in patients with rectal cancer who undergo nCRT. Full article
(This article belongs to the Section Oncology)
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<p>Flowchart of the study design with inclusion and exclusion criteria. * No pre-nCRT or post-nCRT CT images. nCRT = neoadjuvant chemoradiotherapy, SMI = skeletal muscle index.</p>
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<p>Assessment of body composition through computed tomography (CT) images. (<b>A</b>) CT images of patients classified with volumetric sarcopenia. (<b>B</b>) CT images of patients classified with volumetric non-sarcopenia. The green line marks the L3 vertebral level, while the region between the two blue lines represents the abdominal waist. CT images display skeletal muscle (red), abdominal visceral fat (green), subcutaneous fat (yellow), and visceral organs (purple) within the defined area.</p>
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<p>Kaplan–Meier curves for recurrence-free survival (RFS) and overall survival (OS). (<b>A</b>) RFS based on the pre-nCRT volumetric skeletal muscle index (SMI). (<b>B</b>) OS according to the pre-nCRT volumetric SMI. (<b>C</b>) RFS according to volumetric SMI change types (increase or reduction in the SMI of over 5%). (<b>D</b>) OS based on volumetric SMI change types. <span class="html-italic">p</span>-values are from the log-rank test.</p>
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10 pages, 1203 KiB  
Article
Outcomes of Ixazomib Treatment in Relapsed and Refractory Multiple Myeloma: Insights from Croatian Cooperative Group for Hematologic Diseases (KROHEM)
by Josip Batinić, Barbara Dreta, Goran Rinčić, Antonia Mrdeža, Karla Mišura Jakobac, Delfa Radić Krišto, Milan Vujčić, Mario Piršić, Željko Jonjić, Vlatka Periša, Jasminka Sinčić Petričević, Božena Coha, Hrvoje Holik, Toni Valković, Marija Stanić, Ivan Krečak, Ante Stojanović, Domagoj Sajfert and Sandra Bašić-Kinda
Medicina 2024, 60(11), 1905; https://doi.org/10.3390/medicina60111905 - 20 Nov 2024
Viewed by 248
Abstract
Background and Objectives: Ixazomib, used in combination with lenalidomide and dexamethasone (IRd), has shown efficacy in clinical trials for relapsed/refractory multiple myeloma (RRMM). Materials and Methods: This study evaluates the real-world effectiveness and safety of IRd in Croatian RRMM patients. A [...] Read more.
Background and Objectives: Ixazomib, used in combination with lenalidomide and dexamethasone (IRd), has shown efficacy in clinical trials for relapsed/refractory multiple myeloma (RRMM). Materials and Methods: This study evaluates the real-world effectiveness and safety of IRd in Croatian RRMM patients. A retrospective analysis was conducted on 164 RRMM patients treated with ixazomib at nine Croatian haematology centres from November 2016 to February 2023. Data on patient demographics, treatment regimens, and outcomes were collected and analysed using Kaplan–Meier survival curves and Cox proportional hazards models in R. The median age at ixazomib initiation was 66 years (range 40–91). Results: The overall response rate (ORR) was 65.8%, with 42% of patients achieving a very good partial response (VGPR) or better. The median progression-free survival (PFS) was 15.4 months, while median overall survival (OS) was 28.2 months. Hematologic toxicities included anaemia (53%), neutropenia (50%), and thrombocytopenia (45%). Infective complications, primarily COVID-19 and pneumonia, were reported in 38% of patients. The safety profile was consistent with previous studies, indicating manageable adverse events. Ixazomib-based therapy is effective and well tolerated in a real-world Croatian RRMM population. Conclusions: The findings align with clinical trial results, demonstrating the applicability of ixazomib in routine clinical practice. Further studies are needed to optimise treatment sequencing and improve patient outcomes. Full article
(This article belongs to the Special Issue Cutting-Edge Research in Relapsed and Refractory Multiple Myeloma)
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<p>Progression-free survival (<b>a</b>) and overall survival (<b>b</b>) for the entire study population.</p>
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<p>Progression-free survival (<b>a</b>) and overall survival (<b>b</b>) according to number of previous lines of treatment.</p>
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<p>Overall survival (<b>a</b>) and progression-free survival (<b>b</b>) according to age.</p>
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<p>Overall survival (<b>a</b>) and progression-free survival (<b>b</b>) according to ECOG performance status.</p>
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25 pages, 4018 KiB  
Article
A Transcriptomics-Based Machine Learning Model Discriminating Mild Cognitive Impairment and the Prediction of Conversion to Alzheimer’s Disease
by Min-Koo Park, Jinhyun Ahn, Jin-Muk Lim, Minsoo Han, Ji-Won Lee, Jeong-Chan Lee, Sung-Joo Hwang and Keun-Cheol Kim
Cells 2024, 13(22), 1920; https://doi.org/10.3390/cells13221920 - 19 Nov 2024
Viewed by 218
Abstract
The clinical spectrum of Alzheimer’s disease (AD) ranges dynamically from asymptomatic and mild cognitive impairment (MCI) to mild, moderate, or severe AD. Although a few disease-modifying treatments, such as lecanemab and donanemab, have been developed, current therapies can only delay disease progression rather [...] Read more.
The clinical spectrum of Alzheimer’s disease (AD) ranges dynamically from asymptomatic and mild cognitive impairment (MCI) to mild, moderate, or severe AD. Although a few disease-modifying treatments, such as lecanemab and donanemab, have been developed, current therapies can only delay disease progression rather than halt it entirely. Therefore, the early detection of MCI and the identification of MCI patients at high risk of progression to AD remain urgent unmet needs in the super-aged era. This study utilized transcriptomics data from cognitively unimpaired (CU) individuals, MCI, and AD patients in the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort and leveraged machine learning models to identify biomarkers that differentiate MCI from CU and also distinguish AD from MCI individuals. Furthermore, Cox proportional hazards analysis was conducted to identify biomarkers predictive of the progression from MCI to AD. Our machine learning models identified a unique set of gene expression profiles capable of achieving an area under the curve (AUC) of 0.98 in distinguishing those with MCI from CU individuals. A subset of these biomarkers was also found to be significantly associated with the risk of progression from MCI to AD. A linear mixed model demonstrated that plasma tau phosphorylated at threonine 181 (pTau181) and neurofilament light chain (NFL) exhibit the prognostic value in predicting cognitive decline longitudinally. These findings underscore the potential of integrating machine learning (ML) with transcriptomic profiling in the early detection and prognostication of AD. This integrated approach could facilitate the development of novel diagnostic tools and therapeutic strategies aimed at delaying or preventing the onset of AD in at-risk individuals. Future studies should focus on validating these biomarkers in larger, independent cohorts and further investigating their roles in AD pathogenesis. Full article
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<p>Study design and workflow for identifying RNA biomarkers predictive of MCI or AD. Methods for biomarker identification and functional annotation are depicted in grey round squares. The numbers in parentheses at the bottom indicate the RNA probes that met the selection criteria and were subsequently identified using ML algorithms. Abbreviations: CU (cognitively unimpaired), MCI (mild cognitive impairment), AD (Alzheimer’s disease), DEG (differentially expressed gene), and GSEA (gene set enrichment analysis).</p>
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<p>Comparison of the discriminating performances of multivariate models. (<b>a</b>) Receiver operating characteristic (ROC) curves for RNA biomarkers combined with demographic variables in the CU vs. MCI comparison. (<b>b</b>) ROC curves for RNA biomarkers in combination with demographics and neuropsychological measures in the CU vs. MCI comparison. (<b>c</b>) ROC curves for RNA biomarkers combined with demographic variables in the MCI vs. AD comparison. (<b>d</b>) ROC curves for RNA biomarkers in combination with demographics and neuropsychological measures in the MCI vs. AD comparison.</p>
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<p>Comparison of the discriminating performances of multivariate models. (<b>a</b>) Receiver operating characteristic (ROC) curves for RNA biomarkers combined with demographic variables in the CU vs. MCI comparison. (<b>b</b>) ROC curves for RNA biomarkers in combination with demographics and neuropsychological measures in the CU vs. MCI comparison. (<b>c</b>) ROC curves for RNA biomarkers combined with demographic variables in the MCI vs. AD comparison. (<b>d</b>) ROC curves for RNA biomarkers in combination with demographics and neuropsychological measures in the MCI vs. AD comparison.</p>
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<p>GSEA and gene network analysis for DEGs discriminating MCI from CU individuals. Ten hub genes from upregulated DEGs are displayed in the center small circle, representing those that overlap more than three clusters. Nodes with a deeper red color represent higher rank scores.</p>
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<p>GSEA and gene network analysis for DEGs discriminating AD from MCI. Ten hub genes from upregulated DEGs are displayed in the center small circle, representing those that overlap more than three clusters.</p>
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<p>Sensitivity analysis result. (<b>a</b>) Confusion matrix for the generalized regression; the sensitivity analysis misclassified 26 cases as CU and 22 cases as MCI out of the 712 MCI and 296 CU cases, respectively. (<b>b</b>) ROC curve of the sensitivity analysis, with an AUC of 0.9801.</p>
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<p>Representative Cox proportional hazard curves for MCI-to-AD converters. Expression values normalized using the robust multi-chip average method per each tertile are indicated in figure insets: (<b>a</b>) GPD1; (<b>b</b>) NPPA; (<b>c</b>) CAV1; (<b>d</b>) LILRB3. Year “0” marks the baseline diagnosis. Tick marks represent participants who were AD conversion-free at the last follow-up or who were censored at that time point.</p>
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<p>Prediction of longitudinal neuropsychological score alterations based on baseline plasma protein levels. Trajectories were derived from the LMM, with the baseline plasma pTau181 and NFL levels as predictors, being adjusted for age, sex, ApoE ε4, and years of education. MMSE trajectories were stratified by (<b>a</b>) pTau181 or (<b>b</b>) NFL tertiles, while ADNI-MEM trajectories were stratified by (<b>c</b>) pTau181 or (<b>d</b>) NFL tertiles. The trajectories depict changes in the MMSE or ADNI-MEM scores over time influenced by different tertiles of baseline pTau181 or NFL levels. The slope, indicative of the rate of cognitive decline, appears steeper for individuals with higher protein levels. The red line represents the highest tertile for each protein, while the blue and green lines represent the intermediate and lowest tertiles, respectively. Shaded areas indicate the 95% confidence intervals of the regression lines. This figure displays the mean levels within each covariate (age and years of education), with females as the reference group. The time span is capped at four years, corresponding to four follow-up assessments.</p>
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<p>Prediction of longitudinal neuropsychological score alterations based on baseline plasma protein levels. Trajectories were derived from the LMM, with the baseline plasma pTau181 and NFL levels as predictors, being adjusted for age, sex, ApoE ε4, and years of education. MMSE trajectories were stratified by (<b>a</b>) pTau181 or (<b>b</b>) NFL tertiles, while ADNI-MEM trajectories were stratified by (<b>c</b>) pTau181 or (<b>d</b>) NFL tertiles. The trajectories depict changes in the MMSE or ADNI-MEM scores over time influenced by different tertiles of baseline pTau181 or NFL levels. The slope, indicative of the rate of cognitive decline, appears steeper for individuals with higher protein levels. The red line represents the highest tertile for each protein, while the blue and green lines represent the intermediate and lowest tertiles, respectively. Shaded areas indicate the 95% confidence intervals of the regression lines. This figure displays the mean levels within each covariate (age and years of education), with females as the reference group. The time span is capped at four years, corresponding to four follow-up assessments.</p>
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13 pages, 478 KiB  
Article
N-3 Fatty Acids in Seafood Influence the Association Between the Composite Dietary Antioxidant Index and Depression: A Community-Based Prospective Cohort Study
by Junhwi Moon, Minji Kim and Yangha Kim
Antioxidants 2024, 13(11), 1413; https://doi.org/10.3390/antiox13111413 - 18 Nov 2024
Viewed by 467
Abstract
Accumulating evidence suggests that seafood and its components, such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), are associated with mental health. However, little is known regarding whether the status of n-3 polyunsaturated fatty acids (PUFAs) modify the effect of dietary antioxidants [...] Read more.
Accumulating evidence suggests that seafood and its components, such as eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), are associated with mental health. However, little is known regarding whether the status of n-3 polyunsaturated fatty acids (PUFAs) modify the effect of dietary antioxidants on depression. The main purpose of study is to investigate longitudinal associations between seafood consumption and depression among 2564 participants aged 40–69 years using data from the Korean Genome and Epidemiology Study. The composite dietary antioxidant index (CDAI) and dietary intake were measured by a validated 106-item food frequency questionnaire and depression was assessed using the Beck Depression Inventory (BDI). The Cox’s proportional hazard model was used to examine the risk of depression according to seafood consumption. During an 8-year follow-up period, 165 (11.9%) men and 224 (18.9%) women experienced depression. After adjustment for confounders, the risk of depression was inversely associated with seafood consumption, with a 42% lower risk (HR T5 vs. T1 = 0.58, 95% CI: 0.35–0.98, p = 0.040) only being found among women. In a group with a high n-3 PUFA intake, CDAI scores were negatively correlated with BDI scores (r = −0.146, p < 0.001) among women. Seafood consumption might lead to more favorable outcomes against depression if accompanied by an increased intake of foods that are rich in antioxidants. Full article
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<p>A flowchart of the study population.</p>
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11 pages, 552 KiB  
Article
Development of Imaging Complexity Biomarkers for Prediction of Symptomatic Radiation Pneumonitis in Patients with Non-Small Cell Lung Cancer, Focusing on Underlying Lung Disease
by Jeongeun Hwang, Hakyoung Kim, Joon-Young Moon, Sun Myung Kim and Dae Sik Yang
Life 2024, 14(11), 1497; https://doi.org/10.3390/life14111497 - 17 Nov 2024
Viewed by 350
Abstract
Objectives: We aimed to develop imaging biomarkers to predict radiation pneumonitis (RP) in non-small cell lung cancer (NSCLC) patients undergoing thoracic radiotherapy. We hypothesized that measuring morphometric complexity in the lung using simulation computed tomography may provide objective imaging biomarkers for lung parenchyma [...] Read more.
Objectives: We aimed to develop imaging biomarkers to predict radiation pneumonitis (RP) in non-small cell lung cancer (NSCLC) patients undergoing thoracic radiotherapy. We hypothesized that measuring morphometric complexity in the lung using simulation computed tomography may provide objective imaging biomarkers for lung parenchyma integrity, potentially forecasting the risk of RP. Materials and Methods: A retrospective study was performed on medical records of 175 patients diagnosed with NSCLC who had received thoracic radiotherapy. Three indices were utilized to measure the morphometric complexity of the lung parenchyma: box-counting fractal dimension, lacunarity, and minimum spanning tree (MST) fractal dimension. Patients were dichotomized into two groups at median values. Cox proportional hazard models were constructed to estimate the hazard ratios for grade ≥ 2 or grade ≥ 3 RP. Results and Conclusions: We found significant associations between lung parenchymal morphometric complexity and RP incidence. In univariate Cox-proportional hazard analysis, patients with a lower MST fractal dimension had a significantly higher hazard ratio of 2.296 (95% CI: 1.348–3.910) for grade ≥ 2 RP. When adjusted for age, sex, smoking status, category of the underlying lung disease, category of radiotherapy technique, clinical stage, histology, and DLCO, patients with a lower MST fractal dimension showed a significantly higher hazard ratio of 3.292 (95% CI: 1.722–6.294) for grade ≥ 2 RP and 7.952 (95% CI: 1.722 36.733) for grade ≥ 3 RP than those with a higher MST fractal dimension. Patients with lower lacunarity exhibited a significantly lower hazard ratio of 0.091 (95% CI: 0.015–0.573) for grade ≥ 3 RP in the adjusted model. We speculated that the lung tissue integrity is captured by morphometric complexity measures, particularly by the MST fractal dimension. We suggest the MST fractal dimension as an imaging biomarker for predicting the occurrence of symptomatic RP after thoracic radiotherapy. Full article
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<p>Kaplan–Meier curves for ≥grade 2 RP incidence in patients with higher (2.716–2.833) and lower (2.534–2.716) MST fractal dimension strata. The <span class="html-italic">p</span>-value of a log-rank test is 0.002.</p>
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13 pages, 515 KiB  
Article
Factors Affecting Cancer Mortality in Young Adults: Findings from a Prospective Cohort Study
by Ngoan T. Le, Yen T.-H. Pham, Linh T. Le, Hang V. Dao, Chihaya Koriyama, Toan H. Ha, Maureen Lichtveld, Suresh V. Kuchipudi, Nhi Y.-N. Huynh, Dai D. Nguyen and Hung N. Luu
Cancers 2024, 16(22), 3853; https://doi.org/10.3390/cancers16223853 - 17 Nov 2024
Viewed by 435
Abstract
Background/Objectives: Cancer incidence in young adults or those aged 15–49 years old has increased during the past decade. Knowledge about the risk factors for cancer-related deaths in young adults is limited, particularly in low- and middle-income countries (LMICs). Methods: This analysis was based [...] Read more.
Background/Objectives: Cancer incidence in young adults or those aged 15–49 years old has increased during the past decade. Knowledge about the risk factors for cancer-related deaths in young adults is limited, particularly in low- and middle-income countries (LMICs). Methods: This analysis was based on the Hanoi Prospective Cohort Study, an ongoing study of 39,401 participants aged 15 or older in Northern Vietnam in the 2007–2019 period. A Cox proportional hazard regression model was used to calculate the hazard ratio (HR) and 95% confidence intervals (95% CIs) for the association between potential factors and the risk of cancer-related deaths. Results: With a median follow-up of 11.01 years, we identified 164 deaths in young adults out of 554 total deaths. Overall, family history of cancer (HR = 7.34; 95% CI: 3.30–16.36), drinking alcohol (HR = 1.82; 95% CI: 1.18–2.81), and smoking (HR = 2.22; 95% CI: 1.36–3.63) were found to be risk factors, while drinking coffee was found to be a protective factor (HR = 0.49; 95% CI: 0.24–1.00) for cancer-related deaths in young adults. Young male adults were found to be at a higher risk due to excessive cigarette smoking (HR = 1.91; 95% CI: 1.00–3.68) and alcohol consumption (HR = 2.15; 95% CI: 1.32–3.53) than those aged 50 years and older (HR = 1.36 and 95% CI: 0.96–1.93 and 1.27 and 95% CI: 0.97–1.67, respectively). The risk of death from cancer in women compared with men in the young population was twice as high as that in the older population (HR = 1.18 and 95% CI: 0.72–1.94 vs. 0.47 and 95% CI: 0.35–0.63, respectively). Conclusions: Our data suggest that the young Vietnamese population is vulnerable to the risk of cancer-related deaths and that cancer in women will increase rapidly in the future. Full article
(This article belongs to the Section Cancer Epidemiology and Prevention)
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<p>Distribution of cancer-related deaths by age group in the Hanoi Prospective Cohort Study.</p>
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13 pages, 439 KiB  
Article
Impact of Screening on Mortality for Patients Diagnosed with Hepatocellular Carcinoma in a Safety-Net Healthcare System: An Opportunity for Addressing Disparities
by Kalyani Narra, Madison Hull, Kari J. Teigen, Vedaamrutha Reddy, Jolonda C. Bullock, Riyaz Basha, Nadia Alawi-Kakomanolis, David E. Gerber and Timothy J. Brown
Cancers 2024, 16(22), 3829; https://doi.org/10.3390/cancers16223829 - 14 Nov 2024
Viewed by 474
Abstract
Purpose: We describe the impact of screening on outcomes of patients diagnosed with hepatocellular carcinoma (HCC) in an urban safety-net healthcare system compared to a non-screened cohort diagnosed with HCC. Methods: Patients diagnosed with HCC at John Peter Smith Health Network were identified [...] Read more.
Purpose: We describe the impact of screening on outcomes of patients diagnosed with hepatocellular carcinoma (HCC) in an urban safety-net healthcare system compared to a non-screened cohort diagnosed with HCC. Methods: Patients diagnosed with HCC at John Peter Smith Health Network were identified by querying the hospital tumor registry and allocated to the screened cohort if they had undergone any liver imaging within one year prior to HCC diagnosis, while the remainder were allocated to the non-screened cohort. Kaplan–Meier methods and log-rank tests were used to compare 3-year survival curves from an index date of HCC diagnosis. Cox proportional hazard models were used to calculate unadjusted and adjusted hazard ratios (HRs) and 95% confidence intervals (CIs). The Duffy adjustment was used to address lead-time bias. Results: A total of 158 patients were included (n = 53 screened, n = 105 non-screened). The median overall survival (OS) for the screened cohort was 19.0 months (95% CI: 9.9–NA) and that for the non-screened cohort was 5.4 months (95% CI: 3.7–8.5) [HR death (non-screened vs. screened) = 2.4, 95% CI: 1.6-3.6; log rank p < 0.0001]. The benefit of screening remained after adjusting for lead-time bias (HR 2.19, 95% CI 1.4–3.3, p = 0.0002). Conclusions: In an urban safety-net population, screening for HCC was associated with improved outcomes compared to patients diagnosed with HCC outside of a screening protocol. Full article
(This article belongs to the Special Issue Emerging Trends in Global Cancer Epidemiology: 2nd Edition)
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<p>(<b>A</b>) Kaplan–Meier curve by screening status of 158 patients. The median overall survival for patients in the screened cohort was 19.0 months (95% CI: 9.9—NA), while the median overall survival for patients in the non-screened cohort was 5.4 months (95% CI: 3.7, 8.5) (log-rank <span class="html-italic">p</span> ≤ 0.0001). (<b>B</b>) Kaplan–Meier curve by screening status of 158 patients, adjusted for a presumed lead time (mean sojourn time of 70 days). The median survival for patients in the screened cohort was 17.0 months (95% CI: 7.8—NA). (<b>C</b>) Kaplan–Meier curve by screening status of 158 patients, adjusted for a presumed lead time (mean sojourn time of 140 days). The median survival for patients in the screened cohort was 15.0 months (95% CI: 6.6—N.A).</p>
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14 pages, 1304 KiB  
Article
Peripheral Eosinophil Count May Be the Prognostic Factor for Overall Survival in Patients with Pancreatic Ductal Adenocarcinoma Undergoing Surgical Treatment
by Wojciech Ciesielski, Izabela Kupryś-Lipińska, Anna Kumor-Kisielewska, Oliwia Grząsiak, Julia Borodacz, Sebastian Niedźwiecki, Piotr Hogendorf, Adam Durczyński, Janusz Strzelczyk and Alicja Majos
Biomedicines 2024, 12(11), 2596; https://doi.org/10.3390/biomedicines12112596 - 13 Nov 2024
Viewed by 385
Abstract
(1) Background: The importance of total eosinophil count in peripheral blood (EOS) as a type 2 inflammation marker is known to be fundamental in asthma, chronic sinusitis, and vasculitis. In cancer, despite their questionable antiproliferative effect, their role remains unclear. Our purpose was [...] Read more.
(1) Background: The importance of total eosinophil count in peripheral blood (EOS) as a type 2 inflammation marker is known to be fundamental in asthma, chronic sinusitis, and vasculitis. In cancer, despite their questionable antiproliferative effect, their role remains unclear. Our purpose was to describe the relationship between baseline blood EOS and overall survival (OS) in pancreatic ductal adenocarcinoma (PDAC) patients. (2) Methods: We retrospectively analyzed data from 137 adult patients who underwent surgical treatment for pancreatic ductal adenocarcinoma (PDAC) between the years 2012 and 2019. Patients with no recent history of systemic steroid use and without intraoperative metastases were included. Patients were categorized into two groups based on EOS (≥0.1 G/l and <0.1 G/l). Survival outcomes were analyzed using Cox proportional hazards regression models. (3) Results: According to EOS and PDAC stage, median OS values were as follows: in stage I–III, EOS ≥ 0.1 G/l group: 14.5 months, in stage I–III, EOS < 0.1 G/l group: 8.0 months, in stage IV, EOS ≥ 0.1 G/l group: 7.0 months, and in stage IV, EOS < 0.1 G/l group: 5.0 months. EOS < 0.1 G/l (vs. ≥0.1 G/l) was an independent prognostic factor for OS in both the uni- and multivariate Cox regression, respectively (HR = 1.48, p = 0.035 and HR = 1.57, p = 0.021). (4) Conclusions: Peripheral eosinophilia seems to be a potential independent prognostic factor. Further studies are necessary to confirm this hypothesis, since our findings suggest that type 2 inflammation may be the factor directly or indirectly lengthening the survival of patients with PDAC. Full article
(This article belongs to the Section Cancer Biology and Oncology)
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<p>EOS vs. OS distribution in groups according to stage. (<b>a</b>) stage IV and (<b>b</b>) stages I–III. Cut-off point EOS 0.1 G/l was marked with a horizontal black line.</p>
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<p>Kaplan–Meyer curves for subgroups according to the stage and baseline peripheral eosinophils count (G/l); <span class="html-italic">p</span> = 0,024. “IV” and “I–III” refer to the PDAC stage.</p>
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<p>Odds ratios for all-cause mortality: black line—1-year all-cause mortality, current study; black histogram—blood eosinophilia values dispersion in the current study; grey lines—4-year all-cause mortality, Andersen et al.; grey histogram—blood eosinophilia values dispersion in Andersen et al. study; the histograms of blood eosinophilia are included for illustrative purposes—black for the current study and grey for Andersen et al. study [<a href="#B18-biomedicines-12-02596" class="html-bibr">18</a>].</p>
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17 pages, 1369 KiB  
Article
Can Radiological Renal Artery Parameters Predict Acute Kidney Injury in Infective Endocarditis Surgery?—From Imaging to Outcomes
by Christian Dinges, Elke Boxhammer, Iris Kremser, Katja Gansterer, Johannes Steindl, Nikolaos Schörghofer, Christoph Knapitsch, Reinhard Kaufmann, Uta C. Hoppe, Matthias Hammerer, Klaus Hergan and Bernhard Scharinger
Diagnostics 2024, 14(22), 2527; https://doi.org/10.3390/diagnostics14222527 - 12 Nov 2024
Viewed by 333
Abstract
Background: Infective endocarditis (IE) poses significant challenges in cardiovascular medicine, often necessitating valvular surgery to manage severe complications. Postoperative acute kidney injury (AKI) is a notable complication affecting patient outcomes. While clinical and procedural factors have been well studied, the role of radiological [...] Read more.
Background: Infective endocarditis (IE) poses significant challenges in cardiovascular medicine, often necessitating valvular surgery to manage severe complications. Postoperative acute kidney injury (AKI) is a notable complication affecting patient outcomes. While clinical and procedural factors have been well studied, the role of radiological renal artery parameters in AKI risk remains underexplored. Methods: This retrospective study analyzed 80 patients with IE who underwent valvular surgery from 2013 to 2021, focusing on postoperative AKI as defined by the Kidney Disease: Improving Global Outcomes (KDIGO) criteria. Radiological parameters, including renal artery calcification, renal ostial calcification, the presence of renal infarctions, and additional arteries, were assessed using preoperative computed tomography (CT). Statistical analyses included binary logistic and linear regression models, Kaplan–Meier survival curves, and Cox proportional hazard regression to explore associations between these parameters and AKI incidence, creatinine levels, and mortality. Results: Out of 80 patients, 31 (38.8%) developed AKI. No significant differences were found in baseline characteristics or radiological parameters between the AKI+ and AKI− groups. Binary logistic and linear regression analyses revealed no substantial relationship between anatomical factors and AKI risk or creatinine levels. However, Cox regression identified “additional renal artery” as a significant predictor of 1-month mortality (HR: 1.747, 95% CI: 1.024–2.979, p = 0.041) but not for 6- or 12-month mortality. Conclusions: Radiological anatomical factors, including calcifications and additional arteries, did not significantly impact AKI risk in IE patients undergoing valvular surgery. However, the presence of additional arteries was associated with increased short-term mortality. These findings suggest the need for further research to elucidate factors contributing to AKI and mortality in this context. Full article
(This article belongs to the Special Issue Advances in Cardiovascular Diseases: Diagnosis and Management)
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<p>CT scans show the renal artery ostium region in the sagittal plane to assess the morphology and circumference of calcifications. (<b>A</b>) shows thin linear (eggshell-type) calcifications (score 1), (<b>B</b>) shows thick linear calcifications (score 2), and (<b>C</b>) shows bulky calcifications (score 3) (white arrows).</p>
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<p>Flow chart of study cohort (created with <a href="http://www.BioRender.com" target="_blank">www.BioRender.com</a>); CT: computed tomography; AKI: acute kidney injury.</p>
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<p>Kaplan–Meier curve with corresponding numbers at risk and log–rank tests for detection of short-term morality in dependence of presence or absence of AKI. AKI: acute kidney injury.</p>
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14 pages, 889 KiB  
Article
Long-Term Ozone Exposure, COPD, and Asthma Mortality: A Retrospective Cohort Study in the Republic of Korea
by Min-Seok Kim, Youn-Hee Lim, Jongmin Oh, Jisun Myung, Changwoo Han, Hyun-Joo Bae, Soontae Kim, Yun-Chul Hong and Dong-Wook Lee
Atmosphere 2024, 15(11), 1340; https://doi.org/10.3390/atmos15111340 - 8 Nov 2024
Viewed by 484
Abstract
Ozone concentrations have increased in recent decades, and several studies have reported that long-term exposure to ozone increases the mortality risk induced by respiratory conditions. However, research on cause-specific mortality related to ozone exposure and respiratory diseases remains scarce. We constructed a retrospective [...] Read more.
Ozone concentrations have increased in recent decades, and several studies have reported that long-term exposure to ozone increases the mortality risk induced by respiratory conditions. However, research on cause-specific mortality related to ozone exposure and respiratory diseases remains scarce. We constructed a retrospective cohort of 5,360,032 adults aged ≥ 65 years from the National Health Insurance Service of Republic of Korea, and death certificates were obtained from Statistics Republic of Korea to determine the cause of death between 2010 and 2019. The daily maximum 8 h average levels of ozone during the warm season annually (May–September) and other air pollutants were determined for the residential district. We analyzed the data using a time-varying Cox proportional hazards model with individual- and district-level covariates, incorporating a competing risk framework to address deaths from causes other than chronic obstructive pulmonary disease (COPD) and asthma. In our single-pollutant model with a 3-year moving average, a 1 ppb increase in ozone exposure was associated with a hazard ratio (HR) of 1.011 (95% confidence interval [CI]: 1.008–1.013) for COPD mortality and an HR of 1.016 (95% CI: 1.011–1.022) for asthma mortality. In our model adjusted for the presence of underlying diseases and district-level variables, the HRs were 1.009 (95% CI: 1.008–1.014) for COPD and 1.017 (95% CI: 1.011–1.023) for asthma, respectively. These associations remained robust in our two-pollutant model, except for NO2 and COPD. A linear concentration–response relationship was identified between ozone concentration, COPD, and asthma mortality. In this large nationwide cohort study, long-term exposure to ozone was associated with an increased risk of death from COPD and asthma in older Korean adults. Full article
(This article belongs to the Topic The Effect of Air Pollution on Human Health)
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<p>Depiction of the study population.</p>
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<p>Exposure–response curve between long-term ozone exposure, COPD, and asthma mortality. COPD, chronic obstructive pulmonary disease; O<sub>3</sub>, ozone. Hazard Ratios for COPD and asthma mortality according to the 3-year moving average ozone exposure were estimated with the adjustment of the calendar year, sex, income level, and health insurance eligibility, Charlson Comorbidity Index scores, and variables at the district level such as total population size, proportion of the population aged ≥ 65 years, proportion of the population with educational levels of high school or less, number of hospital beds per 1000 population, annual average temperature, annual average humidity, and standardized smoking rate.</p>
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<p>Stratified analyses of 3-year moving averages of ozone with mortality caused by COPD and asthma for the association between deaths attributable to COPD or asthma and 1 ppb increase in ozone. COPD, chronic obstructive pulmonary disease; HR, hazard ratio; adjusted for calendar year, sex, income level, and health insurance eligibility; Charlson Comorbidity Index scores; and variables at the district level such as total population size, proportion of the population aged ≥ 65 years, proportion of the population with educational levels of high school or less, number of hospital beds per 1000 population, annual average temperature, annual average humidity, and standardized smoking rate.</p>
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10 pages, 458 KiB  
Article
Associations of Left Atrial Volume Index to Left Ventricular Ejection Fraction Ratio with Clinical Outcomes in Transthyretin Cardiac Amyloidosis
by Yeabsra K. Aleligne, Machelle D. Wilson, Martin Cadeiras, Michael Gibson, Shirin Jimenez, Stella Yala, Pablo E. Acevedo, David A. Liem, Julie T. Bidwell and Imo A. Ebong
J. Cardiovasc. Dev. Dis. 2024, 11(11), 363; https://doi.org/10.3390/jcdd11110363 - 8 Nov 2024
Viewed by 410
Abstract
Background: Transthyretin amyloid cardiomyopathy (ATTR-CM) affects all cardiac chambers to cause left ventricular (LV) deformation as well as left atrial (LA) remodeling and functional impairment. We investigated the associations of the LA volume index (LAVI):LV ejection fraction (LVEF) ratio with the increased risk [...] Read more.
Background: Transthyretin amyloid cardiomyopathy (ATTR-CM) affects all cardiac chambers to cause left ventricular (LV) deformation as well as left atrial (LA) remodeling and functional impairment. We investigated the associations of the LA volume index (LAVI):LV ejection fraction (LVEF) ratio with the increased risk of death, heart transplant, or LV assist device implantation (LVAD) in patients with ATTR-CM. Methods: This was a retrospective cohort study involving 69 heart failure (HF) patients with ATTR-CM at an academic medical center between 1 November 2008 and 31 March 2024. ATTR-CM was diagnosed using a technetium–diphosphonate/pyrophosphate scan or an endomyocardial biopsy. The LAVI and LVEF were measured by echocardiography. Cox proportional hazards models were used for the analysis. Results: The mean (SD) age of the participants was 77.5 (9.3) years. Over a median (IQR) follow-up period of 1.96 (0.67–2.82) years, we observed 24 composite events that included twenty-two deaths, two heart transplants, and two LVAD implantations (who subsequently died). In multivariable-adjusted analyses that accounted for age and the glomerular filtration rate, a one-unit increase in the LAVI:LVEF ratio was associated with a doubling of the risk (HR, 95% CI: 2.06, 1.11–3.82) of experiencing the composite outcome. Conclusions: A one-unit increase in the LAVI:LVEF ratio was associated with an increased risk of death, heart transplant, or LVAD implantation in patients with ATTR-CM. Full article
(This article belongs to the Section Cardiovascular Clinical Research)
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<p>The probability of death, heart transplant, or left ventricular assist device implantation for participants with a left atrial volume index (LAVI)/left ventricular ejection fraction (LVEF) ratio above and below the median value. The median value of the LAVI:LVEF was 0.86.</p>
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11 pages, 658 KiB  
Article
Paradoxical Improvement in Malignant Pleural Mesothelioma Outcomes Following Delayed Treatment Initiation
by Ashwin Kulshrestha, Emanuela Taioli, Andrea Wolf, Raja Flores and Stephanie Tuminello
Cancers 2024, 16(22), 3755; https://doi.org/10.3390/cancers16223755 - 7 Nov 2024
Viewed by 456
Abstract
Background/Objectives: Time to treatment initiation (TTI) has been identified as a predictor of survival in many cancers, but its impact on malignant pleural mesothelioma (MPM) is unknown. This study investigates factors influencing TTI in MPM and its association with overall survival. Methods: The [...] Read more.
Background/Objectives: Time to treatment initiation (TTI) has been identified as a predictor of survival in many cancers, but its impact on malignant pleural mesothelioma (MPM) is unknown. This study investigates factors influencing TTI in MPM and its association with overall survival. Methods: The Surveillance, Epidemiology, and End Results (SEER) database was used to obtain data for MPM patients in the United States. TTI was defined as the number of days from diagnosis to initiation of first treatment, and delayed TTI was defined as exceeding the median TTI. Χ2 tests and t-tests compared sociodemographic and clinical differences between early and delayed TTI groups, while Kaplan–Meier and Cox proportional hazards models evaluated relationships between prognostic factors, TTI, and survival. Results: Among 4879 MPM patients, the median TTI was 39 days. Median survival was 10 months among early TTI patients and 13 months among delayed TTI patients. Patients with epithelioid histology were more likely to have delayed TTI, as were patients who received combination therapy or were diagnosed more recently (p < 0.0001). Adjusting for covariates, delayed TTI status remained associated with better survival (HR 0.79, 95% CI: 0.74–0.84). Conclusions: This study presents an important insight into the management of MPM, demonstrating that delayed time to treatment initiation is positively associated with improved overall survival, contrary to findings in most cancers. This finding underscores the importance of comprehensive, multidisciplinary care, as delays due to robust staging evaluations and patient travel to high-volume centers of excellence likely contribute to delays in treatment. Taken together, these results suggest that clinicians should prioritize personalized treatment planning and collaborative care over a push to rapidly initiate treatment to optimize patient outcomes in MPM. Full article
(This article belongs to the Special Issue Research on Clinical Treatment of Mesothelioma)
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<p>Patient selection flowchart (<span class="html-italic">n</span> = 4879).</p>
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<p>Survival probability over time by strata. Median survival: (<b>a</b>) Delayed TTI: 13 months, Early TTI: 10 months (<span class="html-italic">p</span> &lt; 0.0001); (<b>b</b>) Combination therapy: 18.5 months, Systemic therapy only: 10 months, Surgery only: 7 months (<span class="html-italic">p</span> &lt; 0.0001); (<b>c</b>) Biphasic histology: 11 months, Epithelioid histology: 15 months, Fibrous (sarcomatoid) histology: 6 months, Other/unspecified histology: 10 months (<span class="html-italic">p</span> &lt; 0.0001); (<b>d</b>) Black: 11 months, Other: 11 months, White: 11 months (<span class="html-italic">p</span> = 0.8002).</p>
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16 pages, 2053 KiB  
Article
Impact of Precision in Staging Acute Kidney Injury and Chronic Kidney Disease on Treatment Outcomes: An Observational Study
by Olga Endrich, Christos T. Nakas, Karen Triep, Georg M. Fiedler, Jaime J. Caro and Alistair McGuire
Diagnostics 2024, 14(22), 2476; https://doi.org/10.3390/diagnostics14222476 - 6 Nov 2024
Viewed by 457
Abstract
(1) Background: “Kidney Disease: Improving Global Outcomes” (KDIGO) provides guidelines for identifying the stages of acute kidney injury (AKI) and chronic kidney disease (CKD). A data-driven rule-based engine was developed to determine KDIGO staging compared to KD-related keywords in discharge letters. (2) Methods: [...] Read more.
(1) Background: “Kidney Disease: Improving Global Outcomes” (KDIGO) provides guidelines for identifying the stages of acute kidney injury (AKI) and chronic kidney disease (CKD). A data-driven rule-based engine was developed to determine KDIGO staging compared to KD-related keywords in discharge letters. (2) Methods: To assess potential differences in outcomes, we compare the patient subgroups with exact KDIGO staging to imprecise or missing staging for all-cause mortality, in-hospital mortality, selection bias and costs by applying Kaplan–Meier analysis and the Cox proportional hazards regression model. We analysed 63,105 in-patient cases from 2016 to 2023 at a tertiary hospital with AKI, CKD and acute-on-chronic KD. (3) Results: Imprecise and missing CKD staging were associated with an 85% higher risk of all-cause and in-hospital mortality (CI: 1.7 to 2.0 and 1.66 to 2.03, respectively) compared to exact staging for any given disease status; imprecise or missing AKI staging increased in-hospital mortality risk by 56% and 57% (CI: 1.43 to 1.70 and 1.37 to 1.81, respectively) in patients with AKI. (4) Conclusions: Exact staging is associated with better outcomes in KD management. Our study provides valuable insight into potential quality and outcome improvements and lower costs, considering elderly patients, women and patients with acute-on-chronic KD as the most vulnerable. Full article
(This article belongs to the Special Issue Diagnosis and Treatment of Kidney Disease)
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<p>The current process of assessment, treatment, documentation and coding of KD in cases of in-patient hospitalisation. Created in BioRender. Endrich, O. (2024) [<a href="#B33-diagnostics-14-02476" class="html-bibr">33</a>].</p>
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<p>Kaplan–Meier estimates for AKI patients by stage, all-cause (<b>a</b>) and in-hospital (<b>b</b>) mortality.</p>
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<p>Kaplan–Meier estimates for CKD patients by stage, all-cause (<b>a</b>) and in-hospital (<b>b</b>) mortality.</p>
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<p>Kaplan–Meier estimates for all-cause and in-hospital mortality of KDIGO staging for AKI and CKD relative to kidney disease status. S = 0.75 is added as a reference line for ease of interpretability. (<b>a</b>) All-cause, CKD staging; (<b>b</b>) all-cause, AKI staging; (<b>c</b>) in-hospital, CKD staging; (<b>d</b>) in-hospital, AKI staging.</p>
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