Laboratory Tests Haematology
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Evaluation of Abnormal Liver Chemistries
ACG Clinical Guideline: Evaluation of Abnormal Liver Chemistries Paul Y. Kwo, MD, FACG, FAASLD1, Stanley M. Cohen, MD, FACG, FAASLD2, and Joseph K. Lim, MD, FACG, FAASLD3 1Division of Gastroenterology/Hepatology, Department of Medicine, Stanford University School of Medicine, Palo Alto, California, USA; 2Digestive Health Institute, University Hospitals Cleveland Medical Center and Division of Gastroenterology and Liver Disease, Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio, USA; 3Yale Viral Hepatitis Program, Yale University School of Medicine, New Haven, Connecticut, USA. Am J Gastroenterol 2017; 112:18–35; doi:10.1038/ajg.2016.517; published online 20 December 2016 Abstract Clinicians are required to assess abnormal liver chemistries on a daily basis. The most common liver chemistries ordered are serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase and bilirubin. These tests should be termed liver chemistries or liver tests. Hepatocellular injury is defined as disproportionate elevation of AST and ALT levels compared with alkaline phosphatase levels. Cholestatic injury is defined as disproportionate elevation of alkaline phosphatase level as compared with AST and ALT levels. The majority of bilirubin circulates as unconjugated bilirubin and an elevated conjugated bilirubin implies hepatocellular disease or cholestasis. Multiple studies have demonstrated that the presence of an elevated ALT has been associated with increased liver-related mortality. A true healthy normal ALT level ranges from 29 to 33 IU/l for males, 19 to 25 IU/l for females and levels above this should be assessed. The degree of elevation of ALT and or AST in the clinical setting helps guide the evaluation. -
Tumor Destruction and Kinetics of Tumor Cell Death in Two Experimental Mouse Tumors Following Photodynamic Therapy1
[CANCER RESEARCH 45, 572-576, February 1985] Tumor Destruction and Kinetics of Tumor Cell Death in Two Experimental Mouse Tumors following Photodynamic Therapy1 Barbara W. Henderson,2 Stephen M. Waldow, Thomas S. Mang, William R. Potter, Patrick B. Malone, and Thomas J. Dougherty Division ot Radiation Biology, Department of Radiation Medicine, Roswell Park Memorial Institute, Buffalo, New York 14263 ABSTRACT rapid tumor necrosis (8, 11). Preceding tumor necrosis are pronounced changes in the vascular system of the tumor (3, 5, The effect of photodynamic therapy (PDT) on tumor growth 23). as well as on tumor œil survival in vitro and in vivo was studied In vitro, dose-dependent (photosensitizer + light) photody in the EMT-6 and RIF experimental mouse tumor systems. In namic cell killing is characterized by cell lysis within 1 hr after a vitro, RIF cells were more sensitive towards PDT than were lethal PDT dose (1) and can be achieved in all cell types studied EMT-6 cells when incubated with porphyrin (25 u,g/m\, dihema- thus far, normal as well as malignant (2, 6,14). toporphyrin ether) and subsequently given graded doses of light. Despite extensive in vivo and in vitro studies, it has not yet In vivo, both tumor types responded to PDT (EMT-6, dihemato- been established whether tumor cell killing in vivo is governed porphyrin ether, 7.5 mg/kg; RIF, dihematoporphyrin ether, 10 by the same mechanism as is cell killing in vitro. To answer this mg/kg; both followed 24 hr later by 135 J of light at 630 nm/sq question, we studied the relationship between tumor destruction, cm) with severe vascular disruption and subsequent disappear tumor cure, and tumor cell survival kinetics in 2 experimental ance of tumor bulk. -
Understanding Cancer Tutorial Information for Teachers
Understanding Cancer Tutorial Information for Teachers Understanding Cancer Tutorial • This tutorial was adapted from the Understanding Cancer: Cancer Tutorial available at http://www.cancer.gov/cancertopics/ understandingcancer/cancer • There are two forms for this PPT: – Teacher Presentation version (with a script) – Student Handout version (if printing, specify black/ white on print menu) R Understanding Cancer Tutorial Information for Teachers • The National Cancer Institute has produced a series of cancer related PowerPoint tutorials. These are available as downloadable format at http://www.cancer.gov/cancertopics/ understandingcancer. • Each PowerPoint in this series includes a teacher script. Once these have been downloaded, you may modify the slide show and print student handouts. R Understanding Cancer Teacher Information Developed by: Lewis J. Kleinsmith, Ph.D. Donna Kerrigan, M.S. Jeanne Kelly Brian Hollen Discusses and illustrates what cancer is, explains the link between genes and cancer, and discusses what is known about the causes, detection, and diagnosis of the disease. These PowerPoint slides are not locked files. You can mix and match slides from different tutorials as you prepare your own lectures. In the Notes section, you will find explanations of the graphics. The art in this tutorial is copyrighted and may not be reused for commercial gain. Please do not remove the NCI logo or the copyright mark from any slide. These tutorials may be copied only if they are distributed free of charge for educational purposes. R Cancer R Understanding Cancer Developed by: Lewis J. Kleinsmith, Ph.D. Donna Kerrigan, M.S. Jeanne Kelly Brian Hollen Discusses and illustrates what cancer is, explains the link between genes and cancer, and discusses what is known about the causes, detection, and diagnosis of the disease. -
The Role of Antioxidants on Wound Healing: a Review of the Current Evidence
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 15 July 2021 doi:10.20944/preprints202107.0361.v1 Review THE ROLE OF ANTIOXIDANTS ON WOUND HEALING: A REVIEW OF THE CURRENT EVIDENCE. Inés María Comino-Sanz 1*, María Dolores López-Franco1, Begoña Castro2, Pedro Luis Pancorbo-Hidalgo1 1 Department of Nursing, Faculty of Health Sciences, University of Jaén, 23071 Jaén (Spain); [email protected] (IMCS); MDLP ([email protected]); PLPH ([email protected]). 2 Histocell S.L., Bizkaia Science and Technology Park, Derio, Bizkaia (Spain); [email protected] * Correspondence: [email protected]; Tel.: +34-953213627 Abstract: (1) Background: Reactive oxygen species (ROS) play a crucial role in the preparation of the normal wound healing response. Therefore, a correct balance between low or high levels of ROS is essential. Antioxidant dressings that regulate this balance is a target for new therapies. The pur- pose of this review is to identify the compounds with antioxidant properties that have been tested for wound healing and to summarize the available evidence on their effects. (2) Methods: A litera- ture search was conducted and included any study that evaluated the effects or mechanisms of an- tioxidants in the healing process (in vitro, animal models, or human studies). (3) Results: Seven compounds with antioxidant activity were identified (Curcumin, N-acetyl cysteine, Chitosan, Gallic Acid, Edaravone, Crocin, Safranal, and Quercetin) and 46 studies reporting the effects on the healing process of these antioxidants compounds were included. (4) Conclusions: These results highlight that numerous novel investigations are being conducted to develop more efficient systems for wound healing activity. The application of antioxidants is useful against oxidative damage and ac- celerates wound healing. -
Liver Function Tests in Type 2 Sudanese Diabetic Patients
International Journal of Nutrition and Metabolism Vol. 3(2) pp. 17-21, February 2011 Available online http://www.academicjournals.org/ijnam ISSN 2141-2340 ©2011 Academic Journals. Full Length Research Paper Liver function tests in type 2 Sudanese diabetic patients Ayman S. Idris 1*, Koua Faisal Hammad Mekky 1, Badr Eldin Elsonni Abdalla 2 and Khalid Altom Ali 3 1Department of Biochemistry, Faculty of Science and Technology, Al-Neelain University, P. O. Box 12702, Al Baladya St. Khartoum, Sudan. 2Department of Biochemistry, Faculty of Medicine, University of Gezira, Sudan. 3Department of Biochemistry, Faculty of Medicine, International University of Africa, Sudan. Accepted 21 January, 2011 This study was planned to evaluate the liver function in patients with type 2 diabetes mellitus by measuring aspartate aminotransferase (AST), alanine aminotransferase (ALT), gamma glutamyl transpeptidase (GGT), total protein and albumin. The study was carried out in Wad Medani, Abo Agla Diabetes Centre. 50 patients with type 2 diabetes mellitus (23 male and 27 female) were included in the study. Their ages ranged between 43 and 79 years. Thirty matched normal individuals were taken as control group. In the present study, mean values of ALT, AST and GGT were significantly higher in patients than in the control (P<0.001). Total protein and albumin concentrations in patients were lower compared to control group (P<0.01). The mean of serum glucose in patients revealed significant difference (P<0.000) in comparison to the control group. Although the differences were statistically significant, the means of ALT, AST, GGT, total protein and albumin were falling within the normal range. -
The Influence of Cell Cycle Regulation on Chemotherapy
International Journal of Molecular Sciences Review The Influence of Cell Cycle Regulation on Chemotherapy Ying Sun 1, Yang Liu 1, Xiaoli Ma 2 and Hao Hu 1,* 1 Institute of Biomedical Materials and Engineering, College of Materials Science and Engineering, Qingdao University, Qingdao 266071, China; [email protected] (Y.S.); [email protected] (Y.L.) 2 Qingdao Institute of Measurement Technology, Qingdao 266000, China; [email protected] * Correspondence: [email protected] Abstract: Cell cycle regulation is orchestrated by a complex network of interactions between proteins, enzymes, cytokines, and cell cycle signaling pathways, and is vital for cell proliferation, growth, and repair. The occurrence, development, and metastasis of tumors are closely related to the cell cycle. Cell cycle regulation can be synergistic with chemotherapy in two aspects: inhibition or promotion. The sensitivity of tumor cells to chemotherapeutic drugs can be improved with the cooperation of cell cycle regulation strategies. This review presented the mechanism of the commonly used chemotherapeutic drugs and the effect of the cell cycle on tumorigenesis and development, and the interaction between chemotherapy and cell cycle regulation in cancer treatment was briefly introduced. The current collaborative strategies of chemotherapy and cell cycle regulation are discussed in detail. Finally, we outline the challenges and perspectives about the improvement of combination strategies for cancer therapy. Keywords: chemotherapy; cell cycle regulation; drug delivery systems; combination chemotherapy; cancer therapy Citation: Sun, Y.; Liu, Y.; Ma, X.; Hu, H. The Influence of Cell Cycle Regulation on Chemotherapy. Int. J. 1. Introduction Mol. Sci. 2021, 22, 6923. https:// Chemotherapy is currently one of the main methods of tumor treatment [1]. -
Understanding Your Liver Function Results
www.healthinfo.org.nz Understanding your liver function results Your liver is a very important organ that has many jobs. Some of its jobs are to make proteins, make bile to help you digest fats, store energy, and break down some toxins and medicines. Liver function tests are done if you have symptoms of a liver condition or risk factors for liver disease such as fatty liver, viral hepatitis or high alcohol use. They are also checked if you are taking medicines that can affect how your liver works. Terms used Protein: this is the total of all the different types of protein in your blood. Albumin: this is the main protein your liver makes. It goes into your blood and helps to carry many things around your body. Bilirubin: this is something your body makes when it breaks down old red blood cells and replaces them with new ones. Bilirubin gives bile its yellow colour. Alkaline phosphatase (ALP): this is an enzyme in your liver and bones. (An enzyme is a chemical that helps to speed up other chemical processes.) GGT: this stands for gamma glutamyltransferase, which is an enzyme in your liver. ALT: this stands for alanine aminotransferase, which is another enzyme in your liver. AST: this stands for aspartate aminotransferase, which is also an enzyme in your liver. Normal result If you have a copy of your test results, it will show your results and a normal range for each test. The normal ranges may vary depending on your gender and age group and whether you're pregnant or have any underlying health conditions. -
Chapter 1 Cellular Reaction to Injury 3
Schneider_CH01-001-016.qxd 5/1/08 10:52 AM Page 1 chapter Cellular Reaction 1 to Injury I. ADAPTATION TO ENVIRONMENTAL STRESS A. Hypertrophy 1. Hypertrophy is an increase in the size of an organ or tissue due to an increase in the size of cells. 2. Other characteristics include an increase in protein synthesis and an increase in the size or number of intracellular organelles. 3. A cellular adaptation to increased workload results in hypertrophy, as exemplified by the increase in skeletal muscle mass associated with exercise and the enlargement of the left ventricle in hypertensive heart disease. B. Hyperplasia 1. Hyperplasia is an increase in the size of an organ or tissue caused by an increase in the number of cells. 2. It is exemplified by glandular proliferation in the breast during pregnancy. 3. In some cases, hyperplasia occurs together with hypertrophy. During pregnancy, uterine enlargement is caused by both hypertrophy and hyperplasia of the smooth muscle cells in the uterus. C. Aplasia 1. Aplasia is a failure of cell production. 2. During fetal development, aplasia results in agenesis, or absence of an organ due to failure of production. 3. Later in life, it can be caused by permanent loss of precursor cells in proliferative tissues, such as the bone marrow. D. Hypoplasia 1. Hypoplasia is a decrease in cell production that is less extreme than in aplasia. 2. It is seen in the partial lack of growth and maturation of gonadal structures in Turner syndrome and Klinefelter syndrome. E. Atrophy 1. Atrophy is a decrease in the size of an organ or tissue and results from a decrease in the mass of preexisting cells (Figure 1-1). -
The Asymptomatic Outpatient with Abnormal Liver Function Tests 169 Leading to Shortage of Pyridoxal 50-Phosphate, Which Is a Cofactor for Both AST and ALT
The Asymptomatic Outpatient with Abnormal Liver FunctionTests Michael Krier, MD, Aijaz Ahmed, MD* KEYWORDS Aminotransferases (ALT and AST) LFT Alkaline phosphatase Albumin Prothrombin time Traditionally, the constellation of biochemistry tests including liver enzymes, total bili- rubin, and hepatic synthetic measures (prothrombin time (PT) and serum albumin level) are referred to as liver function tests (LFTs). Abnormal LFTs can be encountered during primary health care visits, routine blood donation, and insurance screening. A reported 1% to 4% of asymptomatic patients exhibit abnormal LFTs, leading to a size- able number of annual consultations to a gastroenterology and/or hepatology prac- tice.1 A cost-effective and systematic approach is essential to the interpretation of abnormal LFTs.2–7 A review of pattern of abnormal LFTs, detailed medical history, and a comprehensive physical examination help establish a foundation for further indi- vidualized testing. Further investigation often involves biochemical testing for disease- specific markers, radiographic imaging, and even consideration of a liver biopsy. In the following account, markers of hepatic injury are reviewed followed by a discussion on an approach to various patterns of abnormal LFTs in an asymptomatic patient. ABNORMAL LFTS: MARKERS OF HEPATIC INJURY Abnormal LFTs can be found in 2 main predominant patterns of hepatic injury, hepa- tocellular necrosis or cholestasis. Differentiation between these 2 main patterns of hepatic injury provides clues for further testing. However, in practice, patients present with a mixed pattern of hepatic injury. Markers of Hepatocellular Injury Aminotransferases Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) are normally intracellular enzymes with mitochondrial and cytoplasmic forms.8 Their names reflect Division of Gastroenterology and Hepatology, Stanford University School of Medicine, 750 Welch Road, Suite # 210, Stanford, CA 94304, USA * Corresponding author. -
Liver Function Testing
Liver function testing What are liver function tests? Role of the liver A liver function test (LFT) is a blood test that gives an What are liver function tests? indication of whether the liver is functioning properly. The test is also very useful to see if there is active What are the substances damage in the liver (hepatitis) or sluggish bile flow (cholestasis). measured in an LFT blood test and what’s so important about Liver function tests measure the amount of particular them? chemicals in the blood. This gives a gauge of possible damage to liver cells - damage that can be caused by Total protein many things including HCV. So a more correct term for Albumin a liver test would actually be a liver dysfunction test. Globulin It’s important to remember that diagnosis of liver Bilirubin disease depends on a combination of patient history, physical examination, laboratory testing, biopsy and GGT sometimes imaging studies such as ultrasound scans. ALK Phos Diagnosis of hepatitis C usually also involves antibody tests (see Edition 19) or PCR tests (see Edition 20). ALT AST People reading this page should keep in mind that abnormalities within liver tests don’t necessarily point Platelet count to specific diseases. Only a physician who knows all Adult range / normal range the aspects of a specific case can reliably make a diagnosis. What are the substances measured in an LFT blood test and what’s so important about them? Role of the liver Total protein The role of the liver is to keep the body’s complex internal chemistry in balance. -
Study Highlights Potential for 'Liquid Health Check'
Academy of Medical Science press release labels Peer-reviewed? Type of study? Subject of study? Peer-reviewed Experimental study Humans Cells Media release from the University of Cambridge Embargoed until 16:00 (UK) on Monday 2 December 2019 Study highlights potential for ‘liquid health check’ to predict disease risk Proteins in our blood could in the future help provide a comprehensive ‘liquid health check’, assessing our health and predicting the likelihood that we will we will develop a range of diseases, according to research published today in Nature Medicine. Preventative medicine programs, such as the United Kingdom’s National Health Service’s Health Check and Healthier You, are aimed at improving our health and reducing our risk of developing diseases. While such strategies are inexpensive, cost-effective and scalable, they could be made more effective using personalized information about an individual’s health and disease risk. The rise and application of ‘big data’ in healthcare, assessing and analyzing detailed, large-scale datasets makes it increasingly feasible to make predictions about health and disease outcomes and enable stratified approaches to prevention and clinical management. Now, an international team of researchers from the UK and USA, working with biotech company SomaLogic, has shown that large-scale measurement of proteins in a single blood test can provide important information about our health and can help to predict a range of different diseases and risk factors. “It is incredible that we can begin to estimate an individual’s body fat percentage and cardiorespiratory fitness level with reasonable accuracy using data from a blood sample. -
Utility of Circulating Tumor DNA in Different Clinical Scenarios of Breast Cancer
cancers Review Utility of Circulating Tumor DNA in Different Clinical Scenarios of Breast Cancer Alexandra Mesquita 1,2,3,*, José Luís Costa 2,3 and Fernando Schmitt 2,3 1 Medical Oncology Department, Hospital Pedro Hispano, Unidade Local Saúde Matosinhos, 4464-513 Senhora da Hora, Portugal 2 Institute of Molecular Pathology and Immunology, University of Porto, 4200-135 Porto, Portugal; [email protected] (J.L.C.); [email protected] (F.S.) 3 Faculty of Medicine, University of Porto, 4200-319 Porto, Portugal * Correspondence: [email protected] Received: 3 November 2020; Accepted: 14 December 2020; Published: 16 December 2020 Simple Summary: This review is focused on the concept of a specific type of “liquid biopsy”, circulating cell-free tumor DNA (ctDNA). It explores the advantages and limitations of using this technique and the latest advances of using it in different clinical scenarios of breast cancer: early, metastatic, and locally advanced disease. It provides the latest advances in this area applied to clinical research and clinical practice, as well as the importance of the collaboration between clinicians and laboratory teams to fully grasp the potential of ctDNA in a precision medicine era. Abstract: Breast cancer is a complex disease whose molecular mechanisms are not completely understood. Developing target therapies is a promising approach. Therefore, understanding the biological behavior of the tumor is a challenge. Tissue biopsy in the metastatic setting remains the standard method for diagnosis. Nevertheless, it has been associated with some disadvantages: It is an invasive procedure, it may not represent tumor heterogeneity, and it does not allow for treatment efficacy to be assessed or early recurrences to be detected.