Hypercholesterolemia Is Correlated With an Increased Risk of Idiopathic Sudden Sensorineural Hearing Loss

Shih‐Lun Chang, Cheng-Kai Hsieh, Kuo-Shu Tseng, Shih‐Feng Weng, Yung‐Song Lin

Ear and Hearing · 2014 · 49 citations · 0 references

Concepts

Abstract

In Brief Objective: Despite the many studies on the associated risk of cardiovascular and cerebrovascular events in patients with hypercholesterolemia (HCh), an association between HCh and the development of idiopathic sudden sensorineural hearing loss (ISSNHL) has been examined in only a few case-control studies. We tested the hypothesis that HCh is a risk factor for developing ISSNHL. Design: Using the Taiwan Longitudinal Health Insurance Database, we conducted a historical prospective cohort study to compare patients diagnosed with HCh from January 1, 2001, through to December 31, 2006 (N = 73,957) with age-matched controls (N = 73,957). We followed each patient until the end of 2009 and evaluated the incidence of ISSNHL for a minimum of 3 years after the initial HCh diagnosis. Results: The incidence of ISSNHL was 1.62 times higher in the HCh cohort than in the non-HCh cohort (10.67 versus 6.61 per 10,000 person-years). Using Cox proportional hazard regressions, the adjusted hazard ratio was 1.60 (95% confidence interval [CI] = 1.39–1.85). An increased risk of developing ISSNHL, with adjusted hazard ratios of 1.48 (95% CI = 1.08–2.04) and 1.69 (95% CI = 1.18–2.43), was observed in HCh patients with newly diagnosed comorbidities of stroke or stroke combined with coronary artery diseases, which are both expected to reflect the severity of HCh. Conclusions: A diagnosis of HCh may indicate an independent risk for ISSNHL. This finding suggests that an underlying vascular mechanism contributes to the development of ISSNHL. We suggest that physicians counsel patients with HCh to seek medical attention if they have hearing impairments, because they may also have an increased risk of developing ISSNHL. Patients with newly diagnosed hypercholesterolemia (HCh) are found to have a 1.62-fold higher incidence of sudden sensorineural hearing loss than patients without HCh. To the best of the authors’ knowledge, despite two case-control studies with limited numbers of patients, this study is the first nationwide, historical prospective cohort study in the literature to examine the risk of sudden sensorineural hearing loss among patients with HCh. The authors also observed an increased risk of developing sudden sensorineural hearing loss in patients with new comorbidities of coronary artery disease and stroke, which are both expected to reflect the severity of HCh. Results of this study suggest an underlying vascular mechanism to sudden sensorineural hearing loss.