MRC Integrative Epidemiology Unit (IEU), University of Bristol, Bristol, UK.
School of Psychological Science, University of Bristol, Bristol, UK.
BMC Med. 2023 Apr 3;21(1):128. doi: 10.1186/s12916-023-02832-8.
Insomnia symptoms are widespread in the population and might have effects on many chronic conditions and their risk factors but previous research has focused on select hypothesised associations/effects rather than taking a systematic hypothesis-free approach across many health outcomes.
We performed a Mendelian randomisation (MR) phenome-wide association study (PheWAS) in 336,975 unrelated white-British UK Biobank participants. Self-reported insomnia symptoms were instrumented by a genetic risk score (GRS) created from 129 single-nucleotide polymorphisms (SNPs). A total of 11,409 outcomes from UK Biobank were extracted and processed by an automated pipeline (PHESANT) for the MR-PheWAS. Potential causal effects (those passing a Bonferroni-corrected significance threshold) were followed up with two-sample MR in MR-Base, where possible.
Four hundred thirty-seven potential causal effects of insomnia symptoms were observed for a diverse range of outcomes, including anxiety, depression, pain, body composition, respiratory, musculoskeletal and cardiovascular traits. We were able to undertake two-sample MR for 71 of these 437 and found evidence of causal effects (with directionally concordant effect estimates across main and sensitivity analyses) for 30 of these. These included novel findings (by which we mean not extensively explored in conventional observational studies and not previously explored using MR based on a systematic search) of an adverse effect on risk of spondylosis (OR [95%CI] = 1.55 [1.33, 1.81]) and bronchitis (OR [95%CI] = 1.12 [1.03, 1.22]), among others.
Insomnia symptoms potentially cause a wide range of adverse health-related outcomes and behaviours. This has implications for developing interventions to prevent and treat a number of diseases in order to reduce multimorbidity and associated polypharmacy.
失眠症状在人群中普遍存在,可能对许多慢性疾病及其危险因素产生影响,但以前的研究集中在选择假设的关联/影响上,而不是在许多健康结果上采取系统的无假设方法。
我们在 336975 名无亲缘关系的白种英国生物库参与者中进行了孟德尔随机化(MR)全基因组关联研究(PheWAS)。自我报告的失眠症状由 129 个单核苷酸多态性(SNP)创建的遗传风险评分(GRS)进行检测。从英国生物库中提取并通过自动流水线(PHESANT)处理了 11409 个结果,用于 MR-PheWAS。对具有 Bonferroni 校正显著性阈值的潜在因果效应(那些通过 Bonferroni 校正显著性阈值的)进行了 MR-Base 中的两样本 MR 随访。
观察到失眠症状对包括焦虑、抑郁、疼痛、身体成分、呼吸、肌肉骨骼和心血管特征在内的各种结果有 437 种潜在的因果效应。我们能够对这 437 个中的 71 个进行两样本 MR,并且发现其中 30 个有因果效应的证据(主要和敏感性分析中的方向一致的效应估计)。其中包括脊椎病(OR[95%CI]=1.55[1.33,1.81])和支气管炎(OR[95%CI]=1.12[1.03,1.22])风险的不良影响等新发现(通过传统观察性研究未广泛探索,也未使用基于系统搜索的 MR 进行探索)。
失眠症状可能导致广泛的不良健康相关结果和行为。这对于开发预防和治疗多种疾病的干预措施以减少多种疾病和相关的多药治疗具有重要意义。