2008
DOI: 10.1016/j.pain.2007.11.012
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A family-based investigation of cold pain tolerance

Abstract: In the present study the question was addressed whether sensitivity to experimental pain stimuli differs between families, which are previously characterized by the degree of cold tolerance (very insensitive or very sensitive) of one family member. A total of 232 healthy medical students were screened for cold pain tolerance employing a cold pressor test. Subsequently 50 of them were investigated in detail under laboratory conditions. The water temperature was 1 degrees C, the maximum time in water 3 min, cold… Show more

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Cited by 36 publications
(27 citation statements)
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“…Although the exact mechanisms remain to be elucidated, higher neuronal affective circuits are thought to play a major role in determining pain tolerance (e.g. descending control) 71 compared to pain thresholds 70 . Thus, centrally mediated processes, involved in the opponent-processes mechanisms, should have a larger impact on pain tolerance than on pain thresholds as reflected in this and other studies.…”
Section: Discussionmentioning
confidence: 99%
“…Although the exact mechanisms remain to be elucidated, higher neuronal affective circuits are thought to play a major role in determining pain tolerance (e.g. descending control) 71 compared to pain thresholds 70 . Thus, centrally mediated processes, involved in the opponent-processes mechanisms, should have a larger impact on pain tolerance than on pain thresholds as reflected in this and other studies.…”
Section: Discussionmentioning
confidence: 99%
“…More worrisome, however, are studies by Kim and colleagues (10, 157), much more highly powered than their predecessors, which failed to see an association of either rs4680 or the high pain sensitivity COMT haplotype with either experimental pain or postsurgical pain in the third molar model. Further, using a family-based design, Birklein and colleagues (165) did not see an association of rs4680 to cold-pressor pain. In addressing the contradictory literature, Kim & Dionne (166) point to very small sample sizes [ n = 3 in the val / val homozygote group in Zubieta et al (162); n ≈ 10/haplotype in the TMD patients of Diatchenko et al (115)], possible ethnic stratification, and the dangers of combining measures of pain threshold and pain tolerance into a single score.…”
Section: Assessing Genetic Factors In Human Pain and Analgesic Variabmentioning
confidence: 95%
“…Despite these intriguing results, the existence of an effect of COMT variation on pain sensitivity is still strongly debated, as some subsequent behavioral studies using larger sample size have failed to show a substantial association (e.g. [13][17]). In the last few years, evidence produced by several groups has suggested that the effect of COMT polymorphism on pain sensitivity is generally not observed for the initial pain provocations, but rather becomes apparent in later phases of a testing session [8], [18], [19].…”
Section: Introductionmentioning
confidence: 99%