Thrombosis in the setting of obesity or inflammatory bowel disease.

Abstract:

:Obesity and inflammatory bowel disease (IBD) are systemic inflammatory disorders that predispose to arterial and venous thrombosis through similar prothrombotic mechanisms. Obesity and IBD are chronic risk factors that lead to a persistently elevated risk of thrombosis, although the thrombotic risk with IBD appears to wax and wane with disease severity. Because of the lack of high-quality evidence to guide management decisions, approaches to the prevention and treatment of thrombosis in patients with obesity or IBD are based on extrapolation from general guidelines for antithrombotic therapy. Obesity alters the pharmacokinetics of some anticoagulant drugs, and IBD patients present the added management challenge of having a high risk of gastrointestinal bleeding while taking anticoagulants. An extended duration of anticoagulant therapy is often recommended for obese or IBD patients with unprovoked venous thromboembolism unless there is a high risk of bleeding, although more data and better biomarkers are needed to determine whether anticoagulation can be safely stopped in a subset of IBD patients during remission of active disease. Most patients with obesity or IBD require thromboprophylaxis in conjunction with hospitalization or surgery, with adjustment of anticoagulant dosing in patients with severe obesity.

journal_name

Blood

journal_title

Blood

authors

Lentz SR

doi

10.1182/blood-2016-05-716720

subject

Has Abstract

pub_date

2016-11-17 00:00:00

pages

2388-2394

issue

20

eissn

0006-4971

issn

1528-0020

pii

128/20/2388

journal_volume

128

pub_type

杂志文章,评审

相关文献

BLOOD文献大全
  • Serotonin 5-HT2B receptors are required for bone-marrow contribution to pulmonary arterial hypertension.

    abstract::Pulmonary arterial hypertension (PAH) is a progressive disease characterized by lung endothelial dysfunction and vascular remodeling. Recently, bone marrow progenitor cells have been localized to PAH lungs, raising the question of their role in disease progression. Independently, serotonin (5-HT) and its receptors hav...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2011-06-358374

    authors: Launay JM,Hervé P,Callebert J,Mallat Z,Collet C,Doly S,Belmer A,Diaz SL,Hatia S,Côté F,Humbert M,Maroteaux L

    更新日期:2012-02-16 00:00:00

  • HHEX promotes myeloid transformation in cooperation with mutant ASXL1.

    abstract::Additional sex combs-like 1 (ASXL1), an epigenetic modulator, is frequently mutated in myeloid neoplasms. Recent analyses of mutant ASXL1 conditional knockin (ASXL1-MT-KI) mice suggested that ASXL1-MT alone is insufficient for myeloid transformation. In our previous study, we used retrovirus-mediated insertional mutag...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.2019004613

    authors: Takeda R,Asada S,Park SJ,Yokoyama A,Becker HJ,Kanai A,Visconte V,Hershberger C,Hayashi Y,Yonezawa T,Tamura M,Fukushima T,Tanaka Y,Fukuyama T,Matsumoto A,Yamasaki S,Nakai K,Yamazaki S,Inaba T,Shibata T,Inoue D,Ho

    更新日期:2020-10-01 00:00:00

  • Hereditary abnormality of platelet aggregation attributable to nucleotide storage pool deficiency.

    abstract::An abnormality of platelet aggregation has been detected in six family members with mild bleeding tendencies. In citrated platelet-rich plasma, primary aggregation induced by ADP or epinephrine and agglutination in response to ristocetin were present but second wave aggregation and aggregation in response to collagen ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Ingerman CM,Smith JB,Shapiro S,Sedar A,Silver MJ

    更新日期:1978-08-01 00:00:00

  • Cbl ubiquitination of p85 is essential for Epo-induced EpoR endocytosis.

    abstract::Erythropoietin (Epo) binding to the Epo receptor (EpoR) elicits downstream signaling that is essential for red blood cell production. One important negative regulatory mechanism to terminate Epo signaling is Epo-induced EpoR endocytosis and degradation. Defects in this mechanism play a key role in the overproduction o...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2013-05-506212

    authors: Bulut GB,Sulahian R,Yao H,Huang LJ

    更新日期:2013-12-05 00:00:00

  • Abnormal T-cell subpopulation function in CLL: excessive suppressor (T gamma) and deficient helper (T mu) activity with respect to B-cell proliferation.

    abstract::T-cell function directly influences several B-cell functions. The effect of T-cell subgroups on B-cell function (DNA synthesis) was evaluated for controls and patients with B-cell type of CLL. Control and CLL intact T cells, T cells with receptors for IgG (T gamma), and T cells without Fc receptors at isolation (T non...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Kay NE

    更新日期:1981-03-01 00:00:00

  • Cyclophosphamide induces type I interferon and augments the number of CD44(hi) T lymphocytes in mice: implications for strategies of chemoimmunotherapy of cancer.

    abstract::In a previous study, we reported that a single injection of cyclophosphamide (CTX) in tumor-bearing mice resulted in tumor eradication when the animals were subsequently injected with tumor-sensitized lymphocytes. Notably, CTX acted by inducing bystander effects on T cells, and the response to the combined CTX/adoptiv...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Schiavoni G,Mattei F,Di Pucchio T,Santini SM,Bracci L,Belardelli F,Proietti E

    更新日期:2000-03-15 00:00:00

  • Functional expression of the eotaxin receptor CCR3 in CD30+ cutaneous T-cell lymphoma.

    abstract::Little is known about mechanisms involved in skin-specific homing of cutaneous T-cell lymphoma (CTCL). Chemokine/chemokine receptor interactions have been implicated in the homing of lymphoma cells to various tissue sites. We investigated tissue samples and tumor cell suspensions of patients with CD30(+) CTCL (n = 8) ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2002-02-0475

    authors: Kleinhans M,Tun-Kyi A,Gilliet M,Kadin ME,Dummer R,Burg G,Nestle FO

    更新日期:2003-02-15 00:00:00

  • Establishment and characterization of a new human leukemia cell line derived from M4E0.

    abstract::A new human leukemia cell line, designated as ME-1, was established from the peripheral blood leukemia cells of a patient with acute myelomonocytic leukemia with eosinophilia (M4E0). This cell line has the characteristic chromosome abnormality of M4E0, inv(16) (p13q22). When cultured in RPMI 1640 medium containing 10%...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Yanagisawa K,Horiuchi T,Fujita S

    更新日期:1991-07-15 00:00:00

  • A crucial role for the homeodomain transcription factor Hhex in lymphopoiesis.

    abstract::The hematopoietically expressed homeobox gene, Hhex, is a transcription factor that is important for development of definitive hematopoietic stem cells (HSCs) and B cells, and that causes T-cell leukemia when overexpressed. Here, we have used an Hhex inducible knockout mouse model to study the role of Hhex in adult he...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2014-06-579813

    authors: Jackson JT,Nasa C,Shi W,Huntington ND,Bogue CW,Alexander WS,McCormack MP

    更新日期:2015-01-29 00:00:00

  • Lymphatic endothelial cells induce tolerance via PD-L1 and lack of costimulation leading to high-level PD-1 expression on CD8 T cells.

    abstract::Lymphatic endothelial cells (LECs) induce peripheral tolerance by direct presentation to CD8 T cells (T(CD8)). We demonstrate that LECs mediate deletion only via programmed cell death-1 (PD-1) ligand 1, despite expressing ligands for the CD160, B- and T-lymphocyte attenuator, and lymphocyte activation gene-3 inhibitor...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2012-04-427013

    authors: Tewalt EF,Cohen JN,Rouhani SJ,Guidi CJ,Qiao H,Fahl SP,Conaway MR,Bender TP,Tung KS,Vella AT,Adler AJ,Chen L,Engelhard VH

    更新日期:2012-12-06 00:00:00

  • Hormone-stimulated heme synthesis by isolated mitochondria.

    abstract::Erythropoietin (Ep), insulin, and prostaglandins E1 and A1 (PGE1, PGA1) enhanced heme synthesis by mitochondria isolated from embryonic and adult mouse liver cells. The combination of Ep with PGE1 had an antagonistic effect, while that of Ep with PGA1 gave an additive result. The capability of isolated human platelet ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Agam G,Djaldetti M

    更新日期:1978-06-01 00:00:00

  • Long noncoding RNAs in biology and hematopoiesis.

    abstract::Genome and transcriptome sequencing have revealed a rich assortment of noncoding RNAs in eukaryote cells, including long noncoding RNAs (lncRNAs), which regulate gene expression independent of protein coding potential. LncRNAs modulate protein coding gene expression in many cell types by regulating multiple processes,...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2013-03-456111

    authors: Paralkar VR,Weiss MJ

    更新日期:2013-06-13 00:00:00

  • The contact activation mechanism in human plasma: activation induced by dextran sulfate.

    abstract::Incubation of normal human plasma with dextran sulfate for 7 min at 4 degrees C generates kallikrein amidolytic activity. No kallikrein activity is generated in factor XII or prekallikrein-deficient plasma and only small amounts (8%) in high molecular weight (HMW) kininogen-deficient plasma. Addition of specific antis...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: van der Graaf F,Keus FJ,Vlooswijk RA,Bouma BN

    更新日期:1982-06-01 00:00:00

  • The inv(11)(p15q22) chromosome translocation of de novo and therapy-related myeloid malignancies results in fusion of the nucleoporin gene, NUP98, with the putative RNA helicase gene, DDX10.

    abstract::The inv(11)(p15q22) is a recurrent chromosomal abnormality associated with de novo and therapy-related myeloid malignancies. Here we report the molecular definition of this chromosomal aberration in four patients. Positional cloning showed the consistent rearrangement of the DDX10 gene on chromosome 11q22, which encod...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Arai Y,Hosoda F,Kobayashi H,Arai K,Hayashi Y,Kamada N,Kaneko Y,Ohki M

    更新日期:1997-06-01 00:00:00

  • Targeting glutaminolysis has antileukemic activity in acute myeloid leukemia and synergizes with BCL-2 inhibition.

    abstract::Cancer cells require glutamine to adapt to increased biosynthetic activity. The limiting step in intracellular glutamine catabolism involves its conversion to glutamate by glutaminase (GA). Different GA isoforms are encoded by the genes GLS1 and GLS2 in humans. Herein, we show that glutamine levels control mitochondri...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2015-01-621870

    authors: Jacque N,Ronchetti AM,Larrue C,Meunier G,Birsen R,Willems L,Saland E,Decroocq J,Maciel TT,Lambert M,Poulain L,Hospital MA,Sujobert P,Joseph L,Chapuis N,Lacombe C,Moura IC,Demo S,Sarry JE,Recher C,Mayeux P,Tambur

    更新日期:2015-09-10 00:00:00

  • Natural history of hereditary spherocytosis during the first year of life.

    abstract::Although hereditary spherocytosis (HS) is a common disorder of the red cell membrane, its clinical and biologic expression at birth and in early infancy has received little attention. In order to obtain insights into the natural history of HS during infancy, we studied 46 neonates, 39 from families in which 1 of the p...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Delhommeau F,Cynober T,Schischmanoff PO,Rohrlich P,Delaunay J,Mohandas N,Tchernia G

    更新日期:2000-01-15 00:00:00

  • Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in Folliculin Interacting Protein 1 deficiency.

    abstract::Agammaglobulinemia is the most profound primary antibody deficiency that can occur due to an early termination of B-cell development. We here investigated 3 novel patients, including the first known adult, from unrelated families with agammaglobulinemia, recurrent infections, and hypertrophic cardiomyopathy (HCM). Two...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.2020006441

    authors: Saettini F,Poli C,Vengoechea J,Bonanomi S,Orellana JC,Fazio G,Rodriguez FH,Noguera LP,Booth CA,Jarur-Chamy V,Shams M,Iascone M,Vukic M,Gasperini S,Quadri M,Barroeta Seijas AB,Rivers E,Mauri M,Badolato R,Cazzaniga G

    更新日期:2020-09-09 00:00:00

  • Residual vein thrombosis to establish duration of anticoagulation after a first episode of deep vein thrombosis: the Duration of Anticoagulation based on Compression UltraSonography (DACUS) study.

    abstract::Residual vein thrombosis (RVT) indicates a prothrombotic state and is useful for evaluating the optimal duration of oral anticoagulant treatment (OAT). Patients with a first episode of deep vein thrombosis, treated with OAT for 3 months, were managed according to RVT findings. Those with RVT were randomized to either ...

    journal_title:Blood

    pub_type: 杂志文章,多中心研究,随机对照试验

    doi:10.1182/blood-2008-01-131656

    authors: Siragusa S,Malato A,Anastasio R,Cigna V,Milio G,Amato C,Bellisi M,Attanzio MT,Cormaci O,Pellegrino M,Dolce A,Casuccio A,Bajardi G,Mariani G

    更新日期:2008-08-01 00:00:00

  • Plasmablasts derive from CD23-negative activated B cells after the extinction of IL-4/STAT6 signaling and IRF4 induction.

    abstract::The terminal differentiation of B cells into antibody-secreting cells (ASCs) is a critical component of adaptive immune responses. However, it is a very sensitive process, which dysfunctions lead to a great variety of lymphoproliferative neoplasia including germinal center-derived lymphomas. To better characterize the...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood.2020005083

    authors: Pignarre A,Chatonnet F,Caron G,Haas M,Desmots-Loyer F,Fest T

    更新日期:2020-11-04 00:00:00

  • A1, a Bcl-2 family member, prolongs cell survival and permits myeloid differentiation.

    abstract::A1, a bcl-2 family member, has been identified as a hematopoietic-specific, early inducible gene. In this study it is shown that stable transfection of A1 into an interleukin-3 (IL-3)-dependent myeloid precursor cell line, 32D c13, leads to a retardation of IL-3 withdrawal-induced cell death similar to that observed w...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Lin EY,Orlofsky A,Wang HG,Reed JC,Prystowsky MB

    更新日期:1996-02-01 00:00:00

  • Fluid shear stress stimulates phosphorylation-dependent nuclear export of HDAC5 and mediates expression of KLF2 and eNOS.

    abstract::Fluid shear stress generated by steady laminar blood flow protects vessels from atherosclerosis. Krüppel-like factor 2 (KLF2) and endothelial nitric oxide synthase (eNOS) are fluid shear stress-responsive genes and key mediators in flow anti-inflammatory and antiatherosclerotic actions. However, the molecular mechanis...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2009-05-224824

    authors: Wang W,Ha CH,Jhun BS,Wong C,Jain MK,Jin ZG

    更新日期:2010-04-08 00:00:00

  • Activation of the human immunodeficiency virus-1 long terminal repeat by respiratory burst oxidants of neutrophils.

    abstract::The human immunodeficiency virus type 1 (HIV-1) long terminal repeat (LTR) introduced in association with the luciferase reporter gene into Jurkat T cells was strongly activated by a combination of human neutrophils and phorbol myristate acetate (PMA). Activation was not observed when normal neutrophils were replaced ...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Klebanoff SJ,Headley CM

    更新日期:1999-01-01 00:00:00

  • Comparison of in vitro growth characteristics of blast cell progenitors (CFU-L) in patients with myelodysplastic syndromes and acute myeloid leukemia.

    abstract::Current knowledge is inadequate to explain the different patterns of blast cell accumulation in myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML). We compared the growth patterns of blast cell progenitors (CFU-L) in 23 patients with advanced MDS and 32 patients with de novo AML. Circulating blast progen...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Aul C,Gattermann N,Schneider W

    更新日期:1992-08-01 00:00:00

  • Nucleotide sequence diversity of hypervariable region 1 of hepatitis C virus in Japanese hemophiliacs with chronic hepatitis C and patients with chronic posttransfusion hepatitis C.

    abstract::Hemophiliac patients with chronic hepatitis C might be exposed to and become infected with multiple hepatitis C virus (HCV) strains by means of frequent use of blood products, even if they are infected with a single subtype of HCV. To test this hypothesis, we analyzed the genetic diversity of hypervariable region 1 (H...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Toyoda H,Fukuda Y,Koyama Y,Nakano I,Kinoshita M,Hadama T,Takamatsu J,Hayakawa T

    更新日期:1996-08-15 00:00:00

  • Regulation of thrombosis and vascular function by protein methionine oxidation.

    abstract::Redox biology is fundamental to both normal cellular homeostasis and pathological states associated with excessive oxidative stress. Reactive oxygen species function not only as signaling molecules but also as redox regulators of protein function. In the vascular system, redox reactions help regulate key physiologic r...

    journal_title:Blood

    pub_type: 杂志文章,评审

    doi:10.1182/blood-2015-01-544676

    authors: Gu SX,Stevens JW,Lentz SR

    更新日期:2015-06-18 00:00:00

  • Polymorphisms at LDLR locus may be associated with coronary artery disease through modulation of coagulation factor VIII activity and independently from lipid profile.

    abstract::High levels of coagulation factor VIII (FVIII) have been associated with cardiovascular disease. Low-density lipoprotein receptor (LDLR) has been recently demonstrated to contribute to FVIII clearance from plasma. The aim of this study was to evaluate 3 single nucleotide polymorphisms in SMARCA4-LDLR gene locus (rs112...

    journal_title:Blood

    pub_type: 杂志文章

    doi:10.1182/blood-2010-03-277079

    authors: Martinelli N,Girelli D,Lunghi B,Pinotti M,Marchetti G,Malerba G,Pignatti PF,Corrocher R,Olivieri O,Bernardi F

    更新日期:2010-12-16 00:00:00

  • Enzymatic treatment of long-term human marrow cultures reveals the preferential location of primitive hemopoietic progenitors in the adherent layer.

    abstract::Recent studies with long-term mouse marrow cultures have indicated the importance of the adherent layer as a primary reservoir of the most primitive stem cells, from which derivative stem cells and more differentiated progenitors are continuously generated. We have now examined the role of the adherent cell layer in l...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Coulombel L,Eaves AC,Eaves CJ

    更新日期:1983-08-01 00:00:00

  • Platelet von Willebrand's antigen II: active release by aggregating agents and a marker of platelet release reaction in vivo.

    abstract::von Willebrand's antigen II (vW AgII), a plasma and platelet antigen immunologically and biochemically distinct from factor-VIII-related antigen (VIIIR:Ag), is decreased in von Willebrand's disease. vW AgII is released from platelets during aggregation and clotting. The release of platelet vW AgII was studied in washe...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Scott JP,Montgomery RR

    更新日期:1981-12-01 00:00:00

  • Use of a generally applicable tissue factor--dependent factor V assay to detect activated protein C-resistant factor Va in patients receiving warfarin and in patients with a lupus anticoagulant.

    abstract::The original activated partial thromboplastin time-based assay for activated protein C (APC)-resistant factor Va (FVa) requires carefully prepared fresh plasma and cannot be used in patients receiving warfarin or in patients with antiphospholipid antibodies. A new test is described here that circumvents these limitati...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Le DT,Griffin JH,Greengard JS,Mujumdar V,Rapaport SI

    更新日期:1995-04-01 00:00:00

  • The active monomeric form of macrophage inflammatory protein-1 alpha interacts with high- and low-affinity classes of receptors on human hematopoietic cells.

    abstract::Macrophage inflammatory protein-1 alpha (MIP-1 alpha) and its human homologue GOS19.1/LD78 are members of the C-C chemokine/intercrine family of secreted proteins. They have proinflammatory properties and also inhibit cell cycle progression of hematopoietic stem cells. Characterization of MIP-1 alpha receptor(s) has b...

    journal_title:Blood

    pub_type: 杂志文章

    doi:

    authors: Avalos BR,Bartynski KJ,Elder PJ,Kotur MS,Burton WG,Wilkie NM

    更新日期:1994-09-15 00:00:00