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Bone grafting is one of the most commonly used options to treat large bone defects. Evidence has shown that vitamin D may affect osseointegration, a major component for successful bone grafting. In vitro studies have proved that implants coated with activated vitamin D stimulate bone production and reduce bone resorption around implants. Animal studies have noticed that oral administration of vitamin D may stimulate bone formation as well as strengthen and support the interaction between bone and implants. Vitamin D insufficiency may affect negatively the cortical peri-implant bone formation, suggesting a negative effect in graft incorporation. Few clinical studies have observed that vitamin D administration enhanced graft incorporation and bone formation, while severe vitamin D deficiency is associated with failed implant osseointegration. Even though there are encouraging results of vitamin D supplementation on graft incorporation in animal studies, the use of vitamin D as an adjuvant in bone grafting procedures cannot be fully supported at the moment. However, there is theoretical support in the use of vitamin D after surgery and the use of bone grafts to support the bone structure, relieve pain and increase graft absorption. Further experimental and clinical studies are required to support the administration of vitamin D and its analogues in such cases.Initially considered to be a respiratory disease, coronavirus disease 2019 (COVID-19) is now recognized as a multisystem disease known to affect all the major organs, including the gastrointestinal system. Based on recent studies, severe acute respiratory syndrome coronavirus 2 causes dysregulation of multiple biological pathways, triggers an exaggerated immune response, and affects multiple organs. The gastrointestinal symptoms in COVID-19 are common but often overlooked. We report the case of a 50-year-old female with a recent history of COVID-19 presenting with complaints of abdominal pain and constipation. Initially, the patient was treated for respiratory symptoms and discharged home. Subsequently, she was re-admitted and diagnosed with colonic obstruction on radiology. Laparotomy revealed descending and sigmoid colonic gangrene requiring left colectomy. This case highlights the uncommon but severe gastrointestinal manifestations of COVID-19.Introduction The relationship between vitamin D deficiency and some diseases (i.e., heart diseases, malignancies, and infectious diseases) has extensively been studied. There is, however, no epidemiological report on whether the familial predisposing factors have any role in the occurrence of vitamin D deficiency. The aim of this study was to investigate the familial aggregation of vitamin D deficiency disorder in the northwest region of Iran. Materials and Methods A total number of 930 individuals from the general population were invited/registered to the Family Medicine Clinic of Asadabadi Hospital, Tabriz University of Medical Sciences, Iran. A blood sample was obtained from subjects to measure the level of vitamin D. The blood tests were carried out by the enzyme-linked immunosorbent assay method using Biorexfars diagnostics in the Asadabadi Hospital Laboratory. We calculated odds ratio (OR) with 95% confidence intervals (95% CI) to estimate the aggregation of vitamin D deficiency among relatives. Results We ascertained 580 cases with vitamin D deficiency disorder representing an overall prevalence rate of 62.4% (95% CI 59-65%) in the northwest region. An aggregation of the vitamin D deficiency was found among brothers (OR = 1.55, 95% CI 0.72-3.32), sisters (OR = 1.24, 95% CI 0.80-1.93), and spouses (OR = 1.18, 95% CI 0.76-1.82) of the cases. Other relatives (including parents, grandparents, grandchildren, aunts, nieces, and nephews) showed no aggregation of deficiency in the family in this study. Conclusion Our findings indicated that there might be an aggregational occurrence of vitamin D deficiency in some of the family members. Therefore, to be able to perform early preventive intervention, we would suggest testing the blood level of vitamin D for brothers, sisters, and spouse if one was diagnosed as having vitamin D deficiency.Introduction Interstitial lung disease (ILD) is a heterogeneous group of over 200 parenchymal lung diseases with a myriad of etiologies. Interstitial lung disease registries from around the world show varying prevalence and incidence of these diseases. selleck products The aim of this study was to determine the epidemiology and characteristics of ILD in Pakistan. Methods This web-based registry, which is the first multicenter registry of ILD from Pakistan, recruited patients from 10 centers of five major cities between January 2016 and March 2019. Results A total of 744 patients were enrolled in the registry. The five most frequent ILDs were idiopathic pulmonary fibrosis (IPF) 34.4%, hypersensitivity pneumonitis (HP) - 17.7%, idiopathic nonspecific interstitial pneumonitis (iNSIP) - 16.8%, connective tissue disease-associated ILD (CTD-ILD) - 16.3%, and sarcoidosis - 9.1%. Conclusion Idiopathic pulmonary fibrosis is the most prevalent ILD in Pakistan, followed by HP and iNSIP. An ongoing prospective registry with longitudinal follow-up will help us further elaborate on the clinical characteristics, treatment, and survival outcome of patients with ILD.Publicly available clinicogenomic data on platforms such as the cancer BioPortal (cBioPortal.org) allow for efficient analyses by researchers with little or no experience working with Big Data. cBioPortal.org also allows for appropriate statistical testing and downloadable images for easy dissemination of findings. In this study, the cBioPortal.org platform was tested and its utility demonstrated by comparing cases of non-small cell lung cancer (NSCLC) with and without epidermal growth factor receptor gene (EGFR) mutations. Patients with EGFR mutations were more likely to be female, of Asian ethnicity, never-smokers, and be diagnosed with lung adenocarcinoma. Metastasis to the pleura, pleural fluid, and liver was common in patients with EGFR mutant NSCLC. On the other hand, lymph node, brain, and adrenal gland metastases were more common in patients with other mutations. While the median overall survival was about the same in the two groups, progression-free survival was significantly shorter in the EGFR mutant group.

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