Pain during the acute phase of Guillain-Barre syndrome

被引:18
作者
Yao, Shaoli [1 ]
Chen, Hongxi [1 ]
Zhang, Qin [1 ]
Shi, Ziyan [1 ]
Liu, Ju [1 ]
Lian, Zhiyun [1 ]
Feng, Huiru [1 ]
Du, Qin [1 ]
Xie, Jinlu [1 ]
Ge, Weihong [2 ]
Zhou, Hongyu [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Neurol, Chengdu, Sichuan, Peoples R China
[2] Hosp Chengdu Off Peoples Govt Tibetan Autonomous, Dept Internal Med, Chengdu, Sichuan, Peoples R China
关键词
albumin; cerebrospinal fluid protein; Guillain-Barre syndrome; pain; uric acid; SERUM URIC-ACID; MULTIPLE-SCLEROSIS; PEROXYNITRITE SCAVENGER; ALBUMIN; CRITERIA;
D O I
10.1097/MD.0000000000011595
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In this study, we tried to describe the characteristics of pain and explore the association between the incidence of pain and abnormal laboratory test results in patients during the acute phase of Guillain-Barre syndrome (GBS). This retrospective cohort study enrolled 252 patients with GBS who were in the acute phase of the disease. We collected data regarding the location and type of pain, the onset time, clinical variables and laboratory tests, including the levels of uric acid (UA), albumin, cerebrospinal fluid protein (CSFP), cerebrospinal fluid glucose (CSFG), fasting glucose upon admission, and blood creatinine. The pain descriptors were compared to the severity of disease and laboratory examination results. Around 34.5% of the patients reported pain during the acute phase of GBS. Pain was negatively correlated with the disease severity during the acute phase. In total, 29 of the 87 (33.3%) patients reported pain during the 2 weeks preceding the onset of weakness. The concentration of CSFP was positively associated with the incidence of pain, while the concentrations of UA and albumin were not correlated with the incidence of pain. We found that 33.3% of the GBS patients experienced pain within 2 weeks of onset, and the pain was positively associated with CSFP concentration but was not correlated with disease severity.
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页数:5
相关论文
共 26 条
[1]   URIC-ACID PROVIDES AN ANTIOXIDANT DEFENSE IN HUMANS AGAINST OXIDANT-CAUSED AND RADICAL-CAUSED AGING AND CANCER - A HYPOTHESIS [J].
AMES, BN ;
CATHCART, R ;
SCHWIERS, E ;
HOCHSTEIN, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (11) :6858-6862
[2]   ASSESSMENT OF CURRENT DIAGNOSTIC-CRITERIA FOR GUILLAIN-BARRE-SYNDROME [J].
ASBURY, AK ;
CORNBLATH, DR .
ANNALS OF NEUROLOGY, 1990, 27 :S21-S24
[3]   Activation of the inducible form of nitric oxide synthase in the brains of patients with multiple sclerosis [J].
Bagasra, O ;
Michaels, FH ;
Zheng, YM ;
Bobroski, LE ;
Spitsin, SV ;
Fu, ZF ;
Tawadros, R ;
Koprowski, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (26) :12041-12045
[4]   Long-term sensory deficit after Guillain-Barre syndrome [J].
Bernsen, RAJAM ;
de Jager, AEJ ;
Schmitz, PIM ;
van der Meché, FGA .
JOURNAL OF NEUROLOGY, 2001, 248 (06) :483-486
[5]   The role of antioxidant supplement in immune system, neoplastic, and neurodegenerative disorders: a point of view for an assessment of the risk/benefit profile [J].
Brambilla, Daria ;
Mancuso, Cesare ;
Scuderi, Mariagrazia Rita ;
Bosco, Paolo ;
Cantarella, Giuseppina ;
Lempereur, Laurence ;
Di Benedetto, Giulia ;
Pezzino, Salvatore ;
Bernardini, Renato .
NUTRITION JOURNAL, 2008, 7 (1)
[6]   URIC-ACID IRON-ION COMPLEXES - A NEW ASPECT OF THE ANTIOXIDANT FUNCTIONS OF URIC-ACID [J].
DAVIES, KJA ;
SEVANIAN, A ;
MUAKKASSAHKELLY, SF ;
HOCHSTEIN, P .
BIOCHEMICAL JOURNAL, 1986, 235 (03) :747-754
[7]   Diagnosis of Guillain-Barre syndrome and validation of Brighton criteria [J].
Fokke, Christiaan ;
van den Berg, Bianca ;
Drenthen, Judith ;
Walgaard, Christa ;
van Doorn, Pieter Antoon ;
Jacobs, Bart Casper .
BRAIN, 2014, 137 :33-43
[8]   Impairment in Guillain-Barre syndrome during the first 2 years after onset: a prospective study [J].
Forsberg, A ;
Press, R ;
Einarsson, U ;
de Pedro-Cuesta, J ;
Holmqvist, LW .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2004, 227 (01) :131-138
[9]   Prospective evaluation of MRI lumbosacral nerve root enhancement in acute Guillain-Barre syndrome [J].
Gorson, KC ;
Ropper, AH ;
Muriello, MA ;
Blair, R .
NEUROLOGY, 1996, 47 (03) :813-817
[10]   Uric acid, a peroxynitrite scavenger, inhibits CNS inflammation, blood-CNS barrier permeability changes, and tissue damage in a mouse model of multiple sclerosis [J].
Hooper, DC ;
Scott, GS ;
Zborek, A ;
Mikheeva, T ;
Kean, RB ;
Koprowski, H ;
Spitsin, SV .
FASEB JOURNAL, 2000, 14 (05) :691-698