Connecticut Convergence Institute for Translation in Regenerative Engineering, School of Medicine, University of Connecticut, Farmington, CT.
Department of Exercise and Sport Science, University of Central Arkansas, Conway, AR.
Rheumatology (Oxford). 2021 Sep 1;60(9):4272-4280. doi: 10.1093/rheumatology/keaa926.
Previous observations suggest an association between Ehlers-Danlos syndrome (EDS) and gastrointestinal (GI), cardiovascular, immune, and autonomic nervous system dysfunction. We sought to determine whether a hospital diagnosis of EDS is associated with a higher prevalence of these manifestations vs hospitalized patients without EDS. We also evaluated hospital outcomes.
A total of 6,021 cases and matched controls were acquired from the 2016 National Inpatient Sample. In total, 2,007 EDS patients were identified via ICD-10 code. After bivariate analyses, multivariate logistic regression models were used to adjust for potential confounders.
GI conditions were found in 44% of EDS patients vs 18% of controls [odds ratio (OR) = 3.57, 95% CI: 3.17, 4.02, P < 0.0001], with irritable bowel syndrome, gastroparesis and coeliac disease strongly associated with EDS. Autonomic dysfunction, including postural orthostatic tachycardia syndrome (POTS), neurocardiogenic syncope and orthostatic hypotension was found in 20% of EDS patients vs 6% of controls (OR = 4.45, 95% CI: 3.71, 5.32, P < 0.0001). EDS patients were more likely to have food allergy (OR = 3.88, 95% CI: 2.65, 5.66, P < 0.0001) and cardiovascular complications such as mitral valve disorders, aortic aneurysm and dysrhythmias (OR = 6.16, 95% CI: 4.60, 8.23, P < 0.0001). These conditions remained highly associated with EDS after considering confounders. EDS patients were 76% more likely to have longer than average hospitalizations (OR = 1.76, 95% CI: 1.54, 2.02, P < 0.0001).
GI, cardiovascular, autonomic and allergic manifestations are significantly more prevalent in EDS patients compared with hospitalized patients without EDS. Physicians should consider EDS in patients with unexplained GI, cardiovascular, autonomic and allergic conditions and exercise precautions when treating EDS patients in a hospital setting.
先前的观察表明,埃勒斯-当洛斯综合征(EDS)与胃肠道(GI)、心血管、免疫和自主神经系统功能障碍有关。我们试图确定医院诊断的 EDS 是否与这些表现的更高患病率相关,而不是没有 EDS 的住院患者。我们还评估了医院的结果。
我们从 2016 年全国住院患者样本中获得了总共 6021 例病例和匹配的对照。总共通过 ICD-10 代码识别了 2007 例 EDS 患者。在进行双变量分析后,使用多变量逻辑回归模型来调整潜在的混杂因素。
GI 疾病在 44%的 EDS 患者中发现,而在 18%的对照组中发现[比值比(OR)=3.57,95%置信区间:3.17,4.02,P<0.0001],其中肠易激综合征、胃轻瘫和乳糜泻与 EDS 密切相关。自主神经功能障碍,包括体位性心动过速综合征(POTS)、神经心源性晕厥和体位性低血压,在 20%的 EDS 患者中发现,而在 6%的对照组中发现(OR=4.45,95%置信区间:3.71,5.32,P<0.0001)。EDS 患者更有可能出现食物过敏(OR=3.88,95%置信区间:2.65,5.66,P<0.0001)和心血管并发症,如二尖瓣疾病、主动脉瘤和心律失常(OR=6.16,95%置信区间:4.60,8.23,P<0.0001)。在考虑混杂因素后,这些情况仍然与 EDS 高度相关。EDS 患者的住院时间比平均住院时间长 76%(OR=1.76,95%置信区间:1.54,2.02,P<0.0001)。
与没有 EDS 的住院患者相比,EDS 患者的 GI、心血管、自主和过敏表现明显更为普遍。当医生治疗医院环境中的 EDS 患者时,医生应考虑在患有不明原因的 GI、心血管、自主和过敏疾病的患者中考虑 EDS,并采取预防措施。