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1.
Article in English | MEDLINE | ID: mdl-39271148

ABSTRACT

BACKGROUND: Immunoglobulin G4-related disease (IgG4-RD) is a fibroinflammatory condition characterized by IgG4-positive plasma cell infiltration that can affect multiple organs, including the cardiovascular system. The diagnosis of IgG4-RD relies on a combination of clinical, serological, radiological, and pathological findings. However, due to the varied and insidious clinical presentations, normal IgG4 levels in a significant percentage of patients, and frequent multi-organ involvement, imaging plays a crucial role in the diagnosis of IgG4-RD. The aim of study is to comprehensively examine the imaging findings in IgG4-related cardiovascular disease for accurate diagnosis and appropriate treatment. METHODS: A systematic search was conducted across electronic databases, PubMed, Scopus, and Web of Sciences, until 1 September 2023, following PRISMA guidelines by searching major databases for studies reporting detailed cardiovascular imaging findings in IgG4-RD. RESULTS: The search yielded 68 studies (60 case reports, 5 case series, 2 cross-sectional, 1 case-control) with 120 cases of cardiovascular IgG4-RD. Most of the cases were male, averaging 62.8 years. The common initial symptoms were dyspnea and chest pain. The most common imaging finding was vasculopathy, including vessel wall thickening, periarteritits, periaortitis, aortitis, stenosis, ectasia, aneurysm formation, intramural hemorrhage, fistula formation, and dissection, followed by pericardial involvement and mediastinal masses. Case series and cross-sectional studies also showed vasculopathy being the most common finding on various imaging modalities, including angiography and PET/CT, highlighting the complex pathology of IgG4-RD. CONCLUSION: This study evaluated current IgG4-RD articles, revealing a higher prevalence in men and vasculopathy as the most common cardiovascular complication.

2.
Clin Case Rep ; 12(8): e9331, 2024 Aug.
Article in English | MEDLINE | ID: mdl-39161673

ABSTRACT

We report a case of a 21-year-old male with stage IIIB sigmoid colon adenocarcinoma who experienced atypical chest pain post-adjuvant chemotherapy with Capecitabine (5-FU prodrug). Evaluation revealed an unexpectedly detected interventricular septum hemangioma. Due to the vasospasm effect of chemotherapy presenting with semi-ischemia, conservative management was chosen for atypical presentation.

3.
BMC Cardiovasc Disord ; 24(1): 299, 2024 Jun 10.
Article in English | MEDLINE | ID: mdl-38858610

ABSTRACT

BACKGROUND: The treatment of choice for Extra-osseous Ewing's sarcoma/primitive neuroectodermal tumor (ES/PNET), a rare neoplasm, is the VAC/IE regimen. This regimen includes Doxorubicin, Vincristine, Cyclophosphamide, Ifosfamide, and Etoposide, all of which have cardiotoxic effects. Myocarditis, a potentially threatening side effect following cancer therapy, can be accurately managed and diagnosed. CASE PRESENTATION: In the current study, we report the case of a 19-year-old female with a mass on the abdominal wall, diagnosed with ES/PNET. She was treated with the VAC/IE regimen. A month after the last session of chemotherapy, she experienced dyspnea. Upon evaluation, a high level of troponin and a low left ventricular ejection fraction (LVEF) were detected via transthoracic echocardiography. She was treated with anti-heart failure drugs, but the response was unsatisfactory. The possibility of Cancer therapy-related myocarditis was suspected, and cardiac magnetic resonance imaging (CMR) confirmed acute myocarditis. This patient exhibited a significant response to intravenous immunoglobulin (IVIG), with her LVEF improving from 30-35% to 50% within three months. CONCLUSION: In this case, based on negative tests and the absence of viral signs and symptoms, Cancer therapy-related myocarditis is highly suspected as the cause of myocarditis. This case underscores the importance of accurately utilizing CMR as a non-invasive method for diagnosing myocarditis. It effectively highlights the identification of reversible myocarditis with appropriate treatment and the notable response to IVIG, suggesting its potential as a favorable treatment for myocarditis in younger patients.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols , Myocarditis , Ventricular Function, Left , Humans , Female , Myocarditis/chemically induced , Myocarditis/diagnosis , Myocarditis/therapy , Myocarditis/diagnostic imaging , Young Adult , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Treatment Outcome , Ventricular Function, Left/drug effects , Sarcoma, Ewing/drug therapy , Sarcoma, Ewing/therapy , Sarcoma, Ewing/diagnosis , Immunoglobulins, Intravenous/administration & dosage , Cardiotoxicity , Stroke Volume , Recovery of Function , Predictive Value of Tests
4.
Biomed Mater ; 19(2)2024 Feb 26.
Article in English | MEDLINE | ID: mdl-38364284

ABSTRACT

Burn wounds are the most destructive and complicated type of skin or underlying soft tissue injury that are exacerbated by a prolonged inflammatory response. Several cell-based therapeutic systems through the culturing of potent stem cells on modified scaffolds have been developed to direct the burn healing challenges. In this context, a new regenerative platform based on boron (B) enriched-acellular sheep small intestine submucosa (AOSIS) scaffold was designed and used as a carrier for mesenchymal stem cells derived from Wharton's jelly (WJMSCs) aiming to promote the tissue healing in burn-induced rat models. hWJMSCs have been extracted from human extra-embryonic umbilical cord tissue. Thereafter, 96 third-degree burned Wistar male rats were divided into 4 groups. The animals that did not receive any treatment were considered as group A (control). Then, group B was treated just by AOSIS scaffold, group C was received cell-seeded AOSIS scaffold (hWJMSCs-AOSIS), and group D was covered by boron enriched-cell-AOSIS scaffold (B/hWJMSCs-AOSIS). Inflammatory factors, histopathological parameters, and the expression levels of epitheliogenic and angiogenic proteins were assessed on 5, 14 and 21 d post-wounding. Application of the B/hWJMSCs-AOSIS on full-thickness skin-burned wounds significantly reduced the volume of neutrophils and lymphocytes at day 21 post-burning, whilst the number of fibroblasts and blood vessels enhanced at this time. In addition, molecular and histological analysis of wounds over time further verified that the addition of boron promoted wound healing, with decreased inflammatory factors, stimulated vascularization, accelerated re-epithelialization, and enhanced expression levels of epitheliogenic genes. In addition, the boron incorporation amplified wound closure via increasing collagen deposition and fibroblast volume and activity. Therefore, this newly fabricated hWJMSCs/B-loaded scaffold can be used as a promising system to accelerate burn wound reconstruction through inflammatory regulation and angiogenesis stimulation.


Subject(s)
Burns , Mesenchymal Stem Cells , Soft Tissue Injuries , Wharton Jelly , Rats , Male , Humans , Animals , Sheep , Boron , Umbilical Cord , Rats, Wistar , Wound Healing , Burns/therapy , Burns/metabolism , Soft Tissue Injuries/metabolism , Mesenchymal Stem Cells/metabolism , Stem Cells
5.
Cell Tissue Bank ; 24(3): 663-681, 2023 Sep.
Article in English | MEDLINE | ID: mdl-36622494

ABSTRACT

Skeletal problems are an increasing issue due to the increase in the global aging population. Different statistics reports show that today, the global population is aging that results in skeletal problems, increased health system costs, and even higher mortality associated with skeletal problems. Common treatments such as surgery and bone grafts are not always effective and in some cases, they can even cause secondary problems such as infections or improper repair. Cell therapy is a method that can be utilized along with common treatments independently. Mesenchymal stem cells (MSCs) are a very important and efficient source in terms of different diseases, especially bone problems. These cells are present in different tissues such as bone marrow, adipose tissue, umbilical cord, placenta, dental pulp, peripheral blood, amniotic fluid and others. Among the types of MSCs, bone marrow mesenchymal stem cells (BMMSCs) are the most widely used source of these cells, which have appeared to be very effective and promising in terms of skeletal diseases, especially compared to the other sources of MSCs. This study focuses on the specific potential and content of BMMSCs from which the specific capacity of these cells originates, and compares their osteogenic potential with other types of MSCs, and also the future directions in the application of BMMSCs as a source for cell therapy.


Subject(s)
Mesenchymal Stem Cells , Osteogenesis , Pregnancy , Female , Humans , Bone and Bones , Placenta , Cells, Cultured , Mesenchymal Stem Cells/metabolism , Bone Marrow Cells/metabolism , Cell Differentiation
6.
Biomed Pharmacother ; 159: 114195, 2023 Mar.
Article in English | MEDLINE | ID: mdl-36630847

ABSTRACT

Multiple sclerosis (MS) is known as a chronic inflammatory disease (CID) that affects the central nervous system and leads to nerve demyelination. However, the exact cause of MS is unknown, but immune system regulation and inhibiting the function of inflammatory pathways may have a beneficial effect on controlling and improving the disease. Studies show that probiotics can alter the gut microbiome, thereby improving and affecting the immune system and inflammatory responses in patients with MS. The results show that probiotics have a good effect on the recovery of patients with MS in humans and animals. The present study investigated the effect of probiotics and possible therapeutic mechanisms of probiotics on immune cells and inflammatory cytokines. This review article showed that probiotics could improve immune cells and inflammatory cytokines in patients with MS and can play an effective role in disease management and control.


Subject(s)
Multiple Sclerosis , Probiotics , Animals , Humans , Multiple Sclerosis/drug therapy , Central Nervous System , Immunity , Probiotics/pharmacology , Probiotics/therapeutic use , Cytokines
7.
Med Biol Eng Comput ; 60(11): 3069-3080, 2022 Nov.
Article in English | MEDLINE | ID: mdl-36066743

ABSTRACT

One of the newest advances in 3D printing is the printing process of bio-scaffolds. The 3D printing of true materials for cartilage repairs accelerates cell growth and proliferation. In this study, a novel biomaterial was developed for the 3D printing of cartilage scaffolds composed of alginate, thymoquinone and halloysite nanotube. Calcium chloride was used as a cross-linker to form hydrogels. Experimental and numerical studies such as scanning electron microscopy, experimental tensile tests, and compression tests, chondrocyte cell seed, and MTT assay were also done. According to the results, alginate and halloysite nanotube increased the printing quality and mechanical performance of biomaterials. Tensile strength in bio-ink with the 30 mg/ml of alginate, 40 mg/ml of halloysite nanotube with 5% of thymoquinone increased up to 372 ± 42 kPa, while compressive stress reached 894 ± 39 kPa. Numerical results indicated that tensile and compressive properties of the scaffold structure depend on the space between printed rows. The best structure was obtained when the distance of rows was chosen at 0.4 mm, and the nozzle diameter was 0.3 mm. Finally, the biomaterial with the 30 mg/ml of alginate, 40 mg/ml of halloysite nanotube with 5% of thymoquinone showed a high mechanical and biological performance, compared to pure alginate bio-scaffolds. Biomaterials included alginic acid sodium salt/thymoquinone/halloysite nanotube mixed and 3D printed in high technology bioprinter, then mechanical and biological properties of printed bio-scaffolds obtained by different experimental tests.


Subject(s)
Alginates , Nanotubes , Alginates/chemistry , Alginates/pharmacology , Alginic Acid , Benzoquinones , Biocompatible Materials/chemistry , Biocompatible Materials/pharmacology , Calcium Chloride , Cartilage , Clay/chemistry , Hydrogels , Nanotubes/chemistry , Printing, Three-Dimensional , Sodium , Tissue Engineering/methods , Tissue Scaffolds/chemistry
8.
Iran J Med Sci ; 43(1): 70-74, 2018 Jan.
Article in English | MEDLINE | ID: mdl-29398754

ABSTRACT

Several techniques have been proposed to prevent hypotension in obstetric patients. Ephedrine and phenylephrine are individually used to prevent maternal hypotension; however, each has its own drawbacks. Some researchers have reported that the infusion of combined ephedrine and phenylephrine immediately after spinal anesthesia for cesarean delivery reduces the incidence of maternal hypotension. Other studies have indicated that the combination is not superior to the infusion of an individual agent. The present study aimed to evaluate the effect of prophylactic infusion of ephedrine and phenylephrine before the induction of spinal anesthesia for cesarean section on maternal hemodynamic. In a randomized, double-blinded clinical trial study, 90 pregnant women that underwent elective cesarean delivery under spinal anesthesia were recruited. Before the spinal anesthesia, the infusion of combined ephedrine and phenylephrine during 15 minutes (study group) or serum NaCl 0.9% (placebo group) was performed. Hemodynamic parameters and fetal blood gas were recorded. The data were analyzed using the SPSS software, version 16.0. The results showed that hypotension and bradycardia after spinal anesthesia were less in the study group. The need for vasopressors and inotropes to treat hypotension, nausea, and vomiting were higher in the placebo group. First- and fifth-minute Apgar scores were higher in the study group. The prophylactic infusion of low-dose ephedrine and phenylephrine before spinal anesthesia for cesarean delivery can be used to decrease the frequency and severity of maternal hypotension and its side effects to the mother and neonate. TRIAL REGISTRATION NUMBER: IRCT201401277013N6.

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