Indifference or hypersensitivity? Solving the riddle of the pain profile in individuals with autism

被引:12
作者
Hoffman, Tseela [1 ]
Bar-Shalita, Tami [2 ,3 ]
Granovsky, Yelena [4 ,5 ]
Gal, Eynat [6 ]
Kalingel-Levi, Merry [6 ]
Dori, Yael [1 ]
Buxbaum, Chen [4 ]
Yarovinsky, Natalya [7 ]
Weissman-Fogel, Irit [1 ]
机构
[1] Univ Haifa, Fac Social Welf & Hlth Sci, Phys Therapy Dept, Abba Khoushy Ave 199, IL-3498838 Haifa, Israel
[2] Tel Aviv Univ, Fac Med, Sch Hlth Profess, Dept Occupat Therapy, Tel Aviv, Israel
[3] Tel Aviv Univ, Sagol Sch Neurosci, Tel Aviv, Israel
[4] Rambam Hlth Care Ctr, Dept Neurol, Haifa, Israel
[5] Technion Israel Inst Technol, Bruce Rappaport Fac Med, Lab Clin Neurophysiol, Haifa, Israel
[6] Univ Haifa, Fac Social Welf & Hlth Sci, Dept Occupat Therapy, Haifa, Israel
[7] Rambam Hlth Care Ctr, Dept Cognit Neurol, Haifa, Israel
基金
以色列科学基金会;
关键词
Pain modulation profile; Pronociception; Pain perception; Autism spectrum disorder; Quantitative sensory testing; GAMMA-AMINOBUTYRIC-ACID; FUNCTIONING AUTISM; POSTOPERATIVE PAIN; YOUNG-CHILDREN; SPECTRUM; ADULTS; MODULATION; BEHAVIORS; GLUTAMATE; BRAIN;
D O I
10.1097/j.pain.0000000000002767
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Excitatory-inhibitory (E/I) imbalance is a mechanism that underlies autism spectrum disorder, but it is not systematically tested for pain processing. We hypothesized that the pain modulation profile (PMP) in autistic individuals is characterized by less efficient inhibitory processes together with a facilitative state, indicative of a pronociceptive PMP. Fifty-two adults diagnosed with autism and 52 healthy subjects, age matched and sex matched, underwent quantitative sensory testing to assess the function of the (1) pain facilitatory responses to phasic, repetitive, and tonic heat pain stimuli and (2) pain inhibitory processes of habituation and conditioned pain modulation. Anxiety, pain catastrophizing, sensory, and pain sensitivity were self-reported. The autistic group reported significantly higher pain ratings of suprathreshold single (P = 0.001), repetitive (46 degrees C- P = 0.018; 49 degrees C- P = 0.003; 52 degrees C- P < 0.001), and tonic (P = 0.013) heat stimuli that were cross correlated (r = 0.48-0.83; P < 0.001) and associated with sensitivity to daily life pain situations (r = 0.39-0.45; P < 0.005) but not with psychological distress levels. Hypersensitivity to experimental pain was attributed to greater autism severity and sensory hypersensitivity to daily stimuli. Subjects with autism efficiently inhibited phasic but not tonic heat stimuli during conditioned pain modulation. In conclusion, in line with the E/I imbalance mechanism, autism is associated with a pronociceptive PMP expressed by hypersensitivity to daily stimuli and experimental pain and less-efficient inhibition of tonic pain. The latter is an experimental pain model resembling clinical pain. These results challenge the widely held belief that individuals with autism are indifferent to pain and should raise caregivers' awareness of pain sensitivity in autism.
引用
收藏
页码:791 / 803
页数:13
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