Literature DB >> 9059316

Postural vasoconstriction and leg ulceration in homozygous sickle cell disease.

J S Mohan1, J M Marshall, H L Reid, P W Thomas, G R Serjeant.   

Abstract

1. Chronic leg ulceration is a major cause of morbidity in patients with homozygous sickle cell disease; the ulcers commonly resolve on bed rest. We have therefore compared the cutaneous vascular response to dependency in three groups of eight patients with sickle cell disease (those with an active ulcer, with an ulcer scar and with no history of ulceration) and in eight subjects with normal haemoglobin and no history of leg ulceration. 2. We monitored, with a laser Doppler flowmeter, the change in red cell (erythrocyte) flux induced in the skin of the leg, at two sites proximal to the malleoli, with the leg horizontal and 5 and 10 min after moving the leg to the dependent position. 3. With the leg horizontal, mean cutaneous red cell flux was substantially higher in normal skin of patients with sickle cell disease than in normal subjects and was higher still at the site of the ulcer or scar. On dependency, red cell flux fell not only in normal subjects but also in the patients with sickle cell disease, both in the normal skin and at the site of the ulcer or scar; there was no difference in any group between the 5- and 10-min values. The fall in red cell flux in normal skin of patients with sickle cell disease was smaller than in normal subjects when considered as a percentage of the control values (32%, 36%, 30% and 61% respectively in sickle cell patients with an active ulcer, with an ulcer scar and with no history of ulceration and in normal subjects), but in absolute terms the falls in red cell flux were similar in sickle cell patients and normal subjects. By contrast, the fall in red cell flux at the ulcer or scar site was greater than in normal skin from sickle cell patients whether considered as a percentage of the control value (48% and 49% respectively in those with an active ulcer or ulcer scar) or in absolute terms. 4. We propose that high resting perfusion is important in patients with sickle cell disease to maintain normal integrity of cutaneous tissue and that pronounced vasoconstriction on dependency hinders the healing and encourages recurrence of leg ulcers.

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Year:  1997        PMID: 9059316     DOI: 10.1042/cs0920153

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  10 in total

1.  Leg ulcers in sickle cell disease.

Authors:  Caterina P Minniti; James Eckman; Paola Sebastiani; Martin H Steinberg; Samir K Ballas
Journal:  Am J Hematol       Date:  2010-10       Impact factor: 10.047

2.  Serial assessment of laser Doppler flow during acute pain crises in sickle cell disease.

Authors:  Patricia Ann Shi; Deepa Manwani; Olugbenga Olowokure; Vijay Nandi
Journal:  Blood Cells Mol Dis       Date:  2014-05-21       Impact factor: 3.039

Review 3.  Interventions for treating leg ulcers in people with sickle cell disease.

Authors:  Arturo J Martí-Carvajal; Jennifer M Knight-Madden; Maria José Martinez-Zapata
Journal:  Cochrane Database Syst Rev       Date:  2021-01-09

4.  Intima-media thickness of the common femoral artery as a marker of leg ulceration in sickle cell disease patients.

Authors:  Oluwagbemiga O Ayoola; Rahman A Bolarinwa; Uvie U Onakpoya; Tewogbade A Adedeji; Chidiogo C Onwuka; Bukunmi M Idowu
Journal:  Blood Adv       Date:  2018-11-27

5.  Vasculopathy, inflammation, and blood flow in leg ulcers of patients with sickle cell anemia.

Authors:  Caterina P Minniti; Kara-Marie H Delaney; Alexander M Gorbach; Dihua Xu; Chyi-Chia Richard Lee; Nitin Malik; Antony Koroulakis; Matthew Antalek; Jordan Maivelett; Marlene Peters-Lawrence; Enrico M Novelli; Sophie M Lanzkron; Karen C Axelrod; Gregory J Kato
Journal:  Am J Hematol       Date:  2013-09-19       Impact factor: 10.047

6.  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

7.  Peripheral vascular response to inspiratory breath hold in paediatric homozygous sickle cell disease.

Authors:  Veline S L'Esperance; Sharon E Cox; David Simpson; Carolyn Gill; Julie Makani; Deogratias Soka; Josephine Mgaya; Fenella J Kirkham; Geraldine F Clough
Journal:  Exp Physiol       Date:  2012-06-01       Impact factor: 2.969

8.  Investigation of Lipid Profile and Clinical Manifestations in SCA Children.

Authors:  Caroline Conceição da Guarda; Sètondji Cocou Modeste Alexandre Yahouédéhou; Rayra Pereira Santiago; Camila Felix de Lima Fernandes; Joelma Santana Dos Santos Neres; Antonio Mateus de Jesus Oliveira; Milena Magalhães Aleluia; Camylla Vilas Boas Figueiredo; Cleverson Alves Fonseca; Luciana Magalhães Fiuza; Suellen Pinheiro Carvalho; Rodrigo Mota de Oliveira; Valma Maria Lopes Nascimento; Larissa Carneiro Rocha; Marilda Souza Gonçalves
Journal:  Dis Markers       Date:  2020-08-18       Impact factor: 3.434

Review 9.  Interventions for treating leg ulcers in people with sickle cell disease.

Authors:  Arturo J Martí-Carvajal; Jennifer M Knight-Madden; Maria José Martinez-Zapata
Journal:  Cochrane Database Syst Rev       Date:  2014-12-08

10.  Blood viscosity and the expression of inflammatory and adhesion markers in homozygous sickle cell disease subjects with chronic leg ulcers.

Authors:  Andre S Bowers; Harvey L Reid; Andre Greenidge; Clive Landis; Marvin Reid
Journal:  PLoS One       Date:  2013-07-26       Impact factor: 3.240

  10 in total

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