From Department of Anaesthesiology, Waikato Clinical Campus, University of Auckland, Hamilton, New Zealand (J.W.S.) Department of Anaesthesia and Pain Management, Royal Melbourne Hospital, Melbourne, Australia (K.L.) Centre for Integrated Critical Care (K.L.) Department of Pharmacology and Therapeutics (K.L.) Department of Paediatrics (A.J.D., D.J.A., P.J.L.) Department of Medical Biology (M.B.), The University of Melbourne, Melbourne, Australia Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia (K.L.) Department of Anaesthesia, Royal Children's Hospital, Melbourne, Australia (A.J.D.) Murdoch Children's Research Institute, Melbourne, Australia (A.J.D., D.J.A.) Royal Children's Hospital, Melbourne, Australia (D.J.A.) Population Health and Immunity Division (P.D., M.B.) Bioinformatics Division (V.L.), The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia Bruce Lefroy Centre for Genetic Health Research, Murdoch Children's Research Institute, Melbourne, Australia (P.J.L.).
Anesthesiology. 2019 Nov;131(5):974-982. doi: 10.1097/ALN.0000000000002877.
Intraoperative awareness with recall while under apparently adequate general anesthesia is a rare, unexplained, and often very distressing phenomenon. It is possible that a relatively small number of genetic variants might underlie the failure of general anesthetic drugs to adequately suppress explicit memory formation and recall in the presence of apparently adequate anesthesia concentrations.
The authors recruited 12 adult patients who had experienced an episode of intraoperative awareness with recall (compared with 12 controls), performed whole exome sequencing, and applied filtering to obtain a set of genetic variants that might be associated with intraoperative awareness with recall. The criteria were that the variant (1) had a minor allele frequency less than 0.1% in population databases, (2) was within exonic or splicing regions, (3) caused a nonsynonymous change, (4) was predicted to be functionally damaging, (5) was expressed in the top 50% of genes expressed in the brain, and (6) was within genes in Kyoto Encyclopedia of Genes and Genomes pathways associated with general anesthesia, drug metabolism, arousal, and memory.
The authors identified 29 rare genetic variants in 27 genes that were absent in controls and could plausibly be associated with this disorder. One variant in CACNA1A was identified in two patients and two different variants were identified in both CACNA1A and CACNA1S. Of interest was the relative overrepresentation of variants in genes encoding calcium channels and purinergic receptors.
Within the constraints of the filtering process used, the authors did not find any single gene variant or gene that was strongly associated with intraoperative awareness with recall. The authors report 27 candidate genes and associated pathways identified in this pilot project as targets of interest for future larger biologic and epidemiologic studies.
在看似足够的全身麻醉下出现回忆性术中知晓是一种罕见、无法解释且常常令人深感痛苦的现象。在看似足够的麻醉浓度下,少数遗传变异可能导致全身麻醉药物无法充分抑制显性记忆的形成和回忆。
作者招募了 12 名经历过术中知晓伴回忆的成年患者(与 12 名对照相比),进行了全外显子组测序,并应用过滤方法获得了一组可能与术中知晓伴回忆相关的遗传变异。入选标准为:(1)变异在人群数据库中的次要等位基因频率小于 0.1%;(2)位于外显子或剪接区;(3)引起非同义变化;(4)预测具有功能破坏性;(5)在大脑中表达量最高的 50%基因中表达;(6)位于与全身麻醉、药物代谢、觉醒和记忆相关的京都基因与基因组百科全书通路基因内。
作者在 27 个基因中确定了 29 个在对照组中不存在且可能与该疾病相关的罕见遗传变异。CACNA1A 基因中的一个变异在 2 名患者中发现,CACNA1A 和 CACNA1S 基因中均发现了 2 个不同的变异。有趣的是,编码钙通道和嘌呤能受体的基因中的变异相对过表达。
在使用的过滤过程的限制内,作者没有发现任何与术中知晓伴回忆强烈相关的单一基因变异或基因。作者报告了本试点研究中确定的 27 个候选基因和相关途径,作为未来更大的生物学和流行病学研究的关注目标。