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131 results for “carotid plaque”

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ClinicalTrials.gov20/100

Vitamin E and C to Slow Progression of Common Carotid Artery Plaque Build-Up

ClinicalTrials.gov study NCT00000600. IPD Sharing: Not stated. Countries: 0. Publications: 0.

restrictedIPD-UNDECIDEDFeb 2026View details →
geo20/100

Xenium spatial transcriptomics of human carotid artery plaques

GEO Series GSE294466. Homo sapiens. 32 samples. Type: Other.

openGEO-OpenNov 2025View details →
geo20/100

Gene expression profiling of human atherosclerotic plaque: Carotid plaque

GEO Series GSE24495. Homo sapiens. 113 samples. Type: Expression profiling by array.

openGEO-OpenOct 2011View details →
geo20/100

Multi-omic Landscape of Extracellular Vesicles in Human Carotid Atherosclerotic Plaque Reveals Endothelial Communication Networks

GEO Series GSE270496. Homo sapiens. 40 samples. Type: Non-coding RNA profiling by high throughput sequencing.

openGEO-OpenJul 2025View details →
geo12/100

Macrophage heterogeneity in human carotid artery atherosclerotic plaques: identification of novel markers for M1 and M2 that are independent of the activation status

GEO Series GSE22543. Homo sapiens. 2 samples. Type: Expression profiling by array.

openGEO-OpenJun 2016View details →
zenodo12/100

Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques

<p>Mazzaccaro D, Dolci M, Perego F, Delbue S, Giannetta M, Cardani R, Valentina Renna L, Costa E, Corsi-Romanelli MM, Galli C, Pariani E, Nano G, Clemente C, Basilico N. Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques. Ann Vasc Surg. 2021 Dec 11:S0890-5096(21)00912-2. doi: 10.1016/j.avsg.2021.10.070. Epub ahead of print. PMID: 34902464.</p> <p>Abstract</p> <p><strong>Background:&nbsp;</strong>To investigate the presence of genetic material of viral agents and the serum level of inflammatory cytokines in patients submitted to carotid endarterectomy having vulnerable versus stable atherosclerotic plaques.</p> <p><strong>Methods:&nbsp;</strong>Data of patients consecutively submitted to carotid endarterectomy for a significant stenosis from July 2019 to December 2019 were prospectively collected. The genetic material of Epstein-Barr (EBV), CitoMegalo (CMV), Herpes Simplex (HSV), Varicella-Zoster (VZV) and Influenza (IV) Viruses was searched in the patient&#39;s plaques, both in the &quot;mid&quot; of the plaque and in an adjacent lateral portion of no-plaque area. The serum levels of TNF-&alpha;, IL-1&beta;, IL-6, IL10 and CCL5 were determined. The obtained results were then correlated to the histologic vulnerability of the removed carotid plaque. P values &lt; 0.05 were considered statistically significant.</p> <p><strong>Results:&nbsp;</strong>Data of 50 patients were analyzed. A vulnerable plaque was found in 31 patients (62%). The genome of CMV, HSV, VZV and IV was not found in any of the vascular samples, while the EBV genome was found in the &quot;mid&quot; of 2 vulnerable plaques, but not in their respective control area. Eighty-two percent of patients who did not receive anti-IV vaccination (23/28) had vulnerable carotid plaque, compared with 36% of vaccinated patients (8/22, P = 0.001). Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque (73.6 &plusmn; 238.2 vs. 3.9 &plusmn; 13.1 pg/ml, P= 0.01, and 45.9 &plusmn; 103.6 vs. 10.1 &plusmn; 25.3 pg/ml, P= 0.01, respectively), independent of comorbidities, viral exposure or flu vaccination.</p> <p><strong>Conclusions:&nbsp;</strong>The EBV genome was found in the &quot;core&quot; of 2 vulnerable carotid plaques, but not in their respective adjacent control. Influenza vaccination was associated with a lower incidence of carotid plaque vulnerability. Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque.</p>

restrictedFeb 2022View details →
zenodo12/100

Aortic valve sclerosis as an important predictor of long-term mortality in patients with carotid atheromatous plaque requiring carotid endarterectomy

<p>This record contains raw data related to the article &quot;Aortic valve sclerosis as an important predictor of long-term mortality in patients with carotid atheromatous plaque requiring carotid endarterectomy&quot;.&nbsp;A strong association between aortic valve sclerosis (AVSc), the earliest manifestation of calcific aortic valve disease, and atherosclerosis exists. The aim of the study was to evaluate the predictive capabilities of AVSc on long-term all-cause mortality, in patients requiring carotid endarterectomy (CEA).&nbsp;806 consecutive CEA patients were enrolled. Preoperative echocardiography was used to assess AVSc. Computed tomography angiography was applied for plaque characterization. Kaplan-Meier curves, Cox linear regression, and area under the receiving operator characteristic (AUC) curve analyses were used to evaluate the predictive capability of AVSc. Overall, 348 of 541 patients had AVSc (64%). Age, diabetes, and estimated glomerular filtration rate (eGFR) were associated with AVSc. In the 5-year follow-up, AVSc group had a mortality rate of 16.7% while in no-AVSc group was 7.8%. Independent predictors of all-cause mortality were age, sex, eGFR, left ventricular ejection fraction, and AVSc. After adjustments, AVSc was associated with a significant increase in all-cause mortality risk (hazard ratio, HR = 1.9; 95%CI: 1.04-3.54;&nbsp;<em>p</em>&nbsp;= 0.038). We stratify our cohort based on carotid atheromatous plaque-type: soft, calcified, and mixed-fibrotic. In patients with mixed-fibrotic plaques, the mortality rate of AVSc patients was 15.5% compared to 2.4% in no-AVSc patients. In this group, AVSc was associated with an increased long-term all-cause mortality risk with an adjusted HR of 12.8 (95%CI: 1.71-96.35;&nbsp;<em>p</em>&nbsp;= 0.013), and the AUC, combing eGFR and AVSc was 0.77 (<em>p</em>&nbsp;&lt; 0.001).&nbsp;Our findings indicate that AVSc together with eGFR may be used to improve long-term risk stratification of patients undergoing CEA surgery.</p>

restrictedFeb 2022View details →
zenodo12/100

Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques

<p>Mazzaccaro D, Dolci M, Perego F, Delbue S, Giannetta M, Cardani R, Valentina Renna L, Costa E, Corsi-Romanelli MM, Galli C, Pariani E, Nano G, Clemente C, Basilico N. Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques. Ann Vasc Surg. 2022 May;82:325-333. doi: 10.1016/j.avsg.2021.10.070. Epub 2021 Dec 11. PMID: 34902464.</p> <p>Abstract</p> <p><strong>Background:&nbsp;</strong>To investigate the presence of genetic material of viral agents and the serum level of inflammatory cytokines in patients submitted to carotid endarterectomy having vulnerable versus stable atherosclerotic plaques.</p> <p><strong>Methods:&nbsp;</strong>Data of patients consecutively submitted to carotid endarterectomy for a significant stenosis from July 2019 to December 2019 were prospectively collected. The genetic material of Epstein-Barr (EBV), CitoMegalo (CMV), Herpes Simplex (HSV), Varicella-Zoster (VZV) and Influenza (IV) Viruses was searched in the patient&#39;s plaques, both in the &quot;mid&quot; of the plaque and in an adjacent lateral portion of no-plaque area. The serum levels of TNF-&alpha;, IL-1&beta;, IL-6, IL10 and CCL5 were determined. The obtained results were then correlated to the histologic vulnerability of the removed carotid plaque. P values &lt; 0.05 were considered statistically significant.</p> <p><strong>Results:&nbsp;</strong>Data of 50 patients were analyzed. A vulnerable plaque was found in 31 patients (62%). The genome of CMV, HSV, VZV and IV was not found in any of the vascular samples, while the EBV genome was found in the &quot;mid&quot; of 2 vulnerable plaques, but not in their respective control area. Eighty-two percent of patients who did not receive anti-IV vaccination (23/28) had vulnerable carotid plaque, compared with 36% of vaccinated patients (8/22, P = 0.001). Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque (73.6 &plusmn; 238.2 vs. 3.9 &plusmn; 13.1 pg/ml, P= 0.01, and 45.9 &plusmn; 103.6 vs. 10.1 &plusmn; 25.3 pg/ml, P= 0.01, respectively), independent of comorbidities, viral exposure or flu vaccination.</p> <p><strong>Conclusions:&nbsp;</strong>The EBV genome was found in the &quot;core&quot; of 2 vulnerable carotid plaques, but not in their respective adjacent control. Influenza vaccination was associated with a lower incidence of carotid plaque vulnerability. Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque.</p>

restrictedJan 2023View details →
zenodo12/100

Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques

<p>Mazzaccaro D, Dolci M, Perego F, Delbue S, Giannetta M, Cardani R, Valentina Renna L, Costa E, Corsi-Romanelli MM, Galli C, Pariani E, Nano G, Clemente C, Basilico N. Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques. Ann Vasc Surg. 2022 May;82:325-333. doi: 10.1016/j.avsg.2021.10.070. Epub 2021 Dec 11. PMID: 34902464.</p> <p>Abstract</p> <p><strong>Background:&nbsp;</strong>To investigate the presence of genetic material of viral agents and the serum level of inflammatory cytokines in patients submitted to carotid endarterectomy having vulnerable versus stable atherosclerotic plaques.</p> <p><strong>Methods:&nbsp;</strong>Data of patients consecutively submitted to carotid endarterectomy for a significant stenosis from July 2019 to December 2019 were prospectively collected. The genetic material of Epstein-Barr (EBV), CitoMegalo (CMV), Herpes Simplex (HSV), Varicella-Zoster (VZV) and Influenza (IV) Viruses was searched in the patient&#39;s plaques, both in the &quot;mid&quot; of the plaque and in an adjacent lateral portion of no-plaque area. The serum levels of TNF-&alpha;, IL-1&beta;, IL-6, IL10 and CCL5 were determined. The obtained results were then correlated to the histologic vulnerability of the removed carotid plaque. P values &lt; 0.05 were considered statistically significant.</p> <p><strong>Results:&nbsp;</strong>Data of 50 patients were analyzed. A vulnerable plaque was found in 31 patients (62%). The genome of CMV, HSV, VZV and IV was not found in any of the vascular samples, while the EBV genome was found in the &quot;mid&quot; of 2 vulnerable plaques, but not in their respective control area. Eighty-two percent of patients who did not receive anti-IV vaccination (23/28) had vulnerable carotid plaque, compared with 36% of vaccinated patients (8/22, P = 0.001). Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque (73.6 &plusmn; 238.2 vs. 3.9 &plusmn; 13.1 pg/ml, P= 0.01, and 45.9 &plusmn; 103.6 vs. 10.1 &plusmn; 25.3 pg/ml, P= 0.01, respectively), independent of comorbidities, viral exposure or flu vaccination.</p> <p><strong>Conclusions:&nbsp;</strong>The EBV genome was found in the &quot;core&quot; of 2 vulnerable carotid plaques, but not in their respective adjacent control. Influenza vaccination was associated with a lower incidence of carotid plaque vulnerability. Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque.</p>

restrictedJan 2023View details →
geo12/100

LncRNA expression in the formation of carotid plaque caused by atherosclerosis

GEO Series GSE207252. Homo sapiens. 8 samples. Type: Non-coding RNA profiling by array.

openGEO-OpenJul 2022View details →
zenodo8/100

Association between C‑reactive protein and carotid plaque in mild‑to‑moderate idiopathic pulmonary fibrosis

<p>Raw data related to the article</p> <p>&nbsp;</p> <p>Abstract<br> An association between C-reactive protein (CRP) levels and carotid plaque has never been investigated in idiopathic pulmonary<br> fibrosis (IPF). The aim of this study was to evaluate the extent of carotid atherosclerosis in mild-to-moderate IPF<br> and to assess its relationship to serum CRP. This observational retrospective case&ndash;control study included 60 consecutive<br> IPF patients (73.8 &plusmn; 6.6 years, 45 males) and 60 matched controls, examined between Sep 2017 and Jan 2019. All patients<br> underwent CRP assessment and a carotid Doppler ultrasonography. CRP levels were significantly higher in IPF patients than<br> controls (0.2 &plusmn; 0.09 mg/dl vs 0.09 &plusmn; 0.04 mg/dl, p &lt; 0.0001). A total of 46 plaques were detected, with higher prevalence in<br> IPF patients than controls (38 vs 8, p &lt; 0.0001). On univariate logistic regression the main variables independently associated<br> with carotid plaque were: age (HR 1.09, 95% CI 1.03&ndash;1.16, p = 0.006), hypertension duration (HR 1.05, 95% CI 1.01&ndash;1.09,<br> p = 0.01), diabetes duration (HR 1.09, 95% CI 1.01&ndash;1.18, p = 0.03), LDL-cholesterol (HR 1.07, 95% CI 1.04&ndash;1.10, p &lt; 0.0001)<br> and finally CRP levels (HR 1.73, 95% CI 0.59&ndash;5.00, p &lt; 0.0001). Multivariate logistic regression analysis revealed that<br> LDL-cholesterol (HR 1.05, 95% CI 1.01&ndash;1.08, p = 0.009) and CRP levels (HR 1.43, 95% CI 0.39&ndash;5.19, p &lt; 0.0001) retained<br> statistical significance. Common carotid artery-intima media thickness was significantly correlated with CRP levels in IPF<br> patients (r = 0.86). SerumCRP might represent both an early marker and a potential therapeutic target for carotid atherosclerosis<br> in mild-to-moderate IPF.</p>

restrictedAug 2021View details →

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dandi-nwb
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International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

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OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

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Last verified 2026-04-29Open record