Pain intensity, illness duration, and protein catabolism in temporomandibular disorder patients with chronic muscle pain

被引:0
|
作者
McGregor, NR
Zerbes, M
Niblett, SH
Dunstan, RH
Roberts, TK
Butt, HL
Klineberg, IJ [1 ]
机构
[1] Univ Sydney, Westmead Hosp, Westmead Ctr Oral Hlth, Fac Dent,Jaw Funct & Orofacial Pain Res Unit, Westmead, NSW 2145, Australia
[2] Univ Newcastle, Dept Biol Sci, Newcastle, NSW 2308, Australia
[3] John Hunter Hosp, Hunter Area Pathol Serv HAPS, Newcastle, NSW, Australia
来源
JOURNAL OF OROFACIAL PAIN | 2003年 / 17卷 / 02期
关键词
pain; facial pain; fibromyalgia syndrome; temporomandibular joint dysfunction;
D O I
暂无
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Aims: To investigate whether the duration of chronic pain in temporomandibular disorder (TMD) patients is associated with a net depletion of amino acids, and a distinct Process from pain intensity. Methods: Twenty-nine patients defined by the research diagnostic criteria/TMD as having Type 1a muscle pain (TMD1A group), and 34 age- and sex-matched control subjects, were assessed for variation in urinary organic and amino acid excretion by gas chromatography-mass spectrometry. Results: The TMD1A patients' mean pain intensity, assessed on a visual analog scale (VAS), was SA (95% confidence limits: 4.5 to 6.3), TMD1A illness duration was 5.0 +/- 1.2 (SD) years, number of body areas with pain/subject was 6.3 +/- 2.4 (range 0 to 10), and symptom prevalence from the Symptom Check List-90-Revised (SCL-90-R) was 25.5 +/- 11.3 symptoms/subject, which was higher than the controls (5.2 +/- 5.0 symptoms/subject, P < .001). TMD1A patient illness duration was positively correlated with symptom prevalence and body pain distribution, and all were independent of pain intensity. The TMD1A patients bad: (1) an increased tyrosine:leucine ratio; and (2) reduced leucine concentrations (both P < .001), which suggests deregulated catabolism. Pain intensity was associated with: (1) changes in the multivariate urinary metabolite excretion patterns (P < .001); (2) reduced leucine concentrations (P < .001); and (3) increases in total urinary metabolites (P < .04), and in 2 unidentified molecules, UM28 (P < .001) and CFSUM1 (P < .002). TMD1A illness duration was associated with lower (1) urinary metabolite concentrations and (2) succinic acid and combined glutamine + glutamic acid levels, suggesting a progressive depletion of metabolite reserves. Conclusion: In TMD1A patients, total amino acid excretion was positively correlated with pain intensity and negatively correlated with illness duration, which indicated that illness duration was associated with a different set of metabolic anomalies compared with those identified for pain intensity.
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收藏
页码:112 / 124
页数:13
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