Literature DB >> 7510726

Monitoring the acute phase response to vaso-occlusive crisis in sickle cell disease.

J Stuart1, P C Stone, N O Akinola, J R Gallimore, M B Pepys.   

Abstract

AIMS: To identify suitable acute phase proteins as objective markers of tissue ischaemia during painful vaso-occlusive crises in sickle cell disease.
METHODS: The prodromal and established phases of 14 vaso-occlusive crises were studied longitudinally in 10 patients with sickle cell anaemia. Automated solid phase enzyme immunoassays were used to measure the fast responding acute phase proteins C-reactive protein and serum amyloid A protein. Slower responding glycoproteins (fibrinogen, orosomucoid, sialic acid and concanavalin-A binding) were measured in parallel.
RESULTS: C-reactive protein and serum amyloid A protein increased early in crisis, sometimes within the early (prodromal) phase. Crises that resolved within 24 hours in hospital showed a minor and transient rise compared with crises that required treatment for four days or more. In eight crises treated by patients at home the acute phase response ranged from minor to a level consistent with extensive tissue ischaemia.
CONCLUSIONS: Sensitive enzyme immunoassays for C-reactive protein and serum amyloid A protein are of potential value for monitoring the onset of tissue ischaemia in sickle cell crisis and for confirming subsequent resolution.

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Year:  1994        PMID: 7510726      PMCID: PMC501835          DOI: 10.1136/jcp.47.2.166

Source DB:  PubMed          Journal:  J Clin Pathol        ISSN: 0021-9746            Impact factor:   3.411


  16 in total

1.  Rheological changes in the prodromal and established phases of sickle cell vaso-occlusive crisis.

Authors:  N O Akinola; S M Stevens; I M Franklin; G B Nash; J Stuart
Journal:  Br J Haematol       Date:  1992-08       Impact factor: 6.998

Review 2.  Measurement of sialic acid in serum and urine: clinical applications and limitations.

Authors:  P J Waters; E Lewry; C A Pennock
Journal:  Ann Clin Biochem       Date:  1992-11       Impact factor: 2.057

3.  Red blood cell changes during the evolution of the sickle cell painful crisis.

Authors:  S K Ballas; E D Smith
Journal:  Blood       Date:  1992-04-15       Impact factor: 22.113

4.  Is there an acute-phase response in steady-state sickle cell disease?

Authors:  A Singhal; J F Doherty; J G Raynes; K P McAdam; P W Thomas; B E Serjeant; G R Serjeant
Journal:  Lancet       Date:  1993-03-13       Impact factor: 79.321

5.  Lactic acid dehydrogenase activity and plasma hemoglobin elevations in sickle cell disease.

Authors:  C L Neely; T Wajima; A P Kraus; L W Diggs; L Barreras
Journal:  Am J Clin Pathol       Date:  1969-08       Impact factor: 2.493

6.  Painful crises in sickle cell disease--patients' perspectives.

Authors:  N Murray; A May
Journal:  BMJ       Date:  1988-08-13

7.  Serial plasma fibrinogen changes accompanying sickle cell pain crisis.

Authors:  A A Famodu; M O Adedeji; H L Reid
Journal:  Clin Lab Haematol       Date:  1990

8.  Subclinical ischaemic episodes during the steady state of sickle cell anaemia.

Authors:  N O Akinola; S M Stevens; I M Franklin; G B Nash; J Stuart
Journal:  J Clin Pathol       Date:  1992-10       Impact factor: 3.411

9.  Creatine kinase activity in sickle cell disease.

Authors:  B J Hunt; P Korsah; S Eaton; M Brozovic
Journal:  J Clin Pathol       Date:  1989-07       Impact factor: 3.411

10.  Real-time measurement of serum C-reactive protein in the management of infection in the elderly.

Authors:  M L Cox; A G Rudd; R Gallimore; H M Hodkinson; M B Pepys
Journal:  Age Ageing       Date:  1986-09       Impact factor: 10.668

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  17 in total

1.  Proinflammatory cytokines and the hypermetabolism of children with sickle cell disease.

Authors:  Jacqueline M Hibbert; Lewis L Hsu; Sam J Bhathena; Ikovwa Irune; Bismark Sarfo; Melissa S Creary; Beatrice E Gee; Ali I Mohamed; Iris D Buchanan; Ahmad Al-Mahmoud; Jonathan K Stiles
Journal:  Exp Biol Med (Maywood)       Date:  2005-01

2.  Apolipoprotein A-I and serum amyloid A plasma levels are biomarkers of acute painful episodes in patients with sickle cell disease.

Authors:  Ashaunta Tumblin; Anitaben Tailor; Gerard T Hoehn; A Kyle Mack; Laurel Mendelsohn; Lita Freeman; Xiuli Xu; Alan T Remaley; Peter J Munson; Anthony F Suffredini; Gregory J Kato
Journal:  Haematologica       Date:  2010-04-07       Impact factor: 9.941

3.  Renal amyloidosis in a child with sickle cell anemia.

Authors:  Behçet Simşek; Aysun K Bayazit; Melek Ergin; Mustafa Soran; Hasan Dursun; Yurdanur Kilinc
Journal:  Pediatr Nephrol       Date:  2006-03-29       Impact factor: 3.714

4.  Increased circulating levels of soluble HLA class I heterodimers in patients with sickle cell disease.

Authors:  C Moore; M Ehlayel; J Inostroza; L E Leiva; S Kuvibidila; L Yu; R Gardner; D L Ode; R Warrier; R U Sorensen
Journal:  J Natl Med Assoc       Date:  1998-03       Impact factor: 1.798

Review 5.  The proteome of sickle cell disease: insights from exploratory proteomic profiling.

Authors:  Susan Yuditskaya; Anthony F Suffredini; Gregory J Kato
Journal:  Expert Rev Proteomics       Date:  2010-12       Impact factor: 3.940

6.  Health-related stigma in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl Brewer
Journal:  J Natl Med Assoc       Date:  2010-11       Impact factor: 1.798

7.  Care seeking for pain in young adults with sickle cell disease.

Authors:  Coretta M Jenerette; Cheryl A Brewer; Kenneth I Ataga
Journal:  Pain Manag Nurs       Date:  2013-01-21       Impact factor: 1.929

8.  Histopathology of experimentally induced asthma in a murine model of sickle cell disease.

Authors:  Sandhya D Nandedkar; Thomas R Feroah; William Hutchins; Dorothee Weihrauch; Kameswari S Konduri; Jingli Wang; Robert C Strunk; Michael R DeBaun; Cheryl A Hillery; Kirkwood A Pritchard
Journal:  Blood       Date:  2008-06-25       Impact factor: 22.113

9.  C-reactive protein and interleukin-6 are decreased in transgenic sickle cell mice fed a high protein diet.

Authors:  David R Archer; Jonathan K Stiles; Gale W Newman; Alexander Quarshie; Lewis L Hsu; Phouyong Sayavongsa; Jennifer Perry; Elizabeth M Jackson; Jacqueline M Hibbert
Journal:  J Nutr       Date:  2008-06       Impact factor: 4.798

10.  Erythrocyte Aggregation and Blood Viscosity is Similar in Homozygous Sickle Cell Disease Patients with and without Leg Ulcers.

Authors:  Andre S A Bowers; Walworth W Duncan; D J Pepple
Journal:  Int J Angiol       Date:  2018-02-09
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