Vasovagal syncope (VVS) is a common clinical condition with an estimated lifetime prevalence of 35% (1,2). Although VVS is not associated with an increased rate of mortality, there is a significant deterioration in the quality of life (QoL) in conjunction with the severity and frequency of recurrences (3,4). Existing pharmacological and nonpharmacological therapies for VVS have, if at all, a modest efficacy (5,6). Yoga is one of the most common forms of complementary and alternative medicine therapies and is increasingly being practiced worldwide. Yoga, an ancient Indian practice based on the principles of mind-body medicine, has been observed to have a beneficial effect in hypertension, atrial fibrillation, and postmyocardial infarction rehabilitation (7–9). Several studies have shown yoga to favorably modulate the autonomic system by balancing the central and peripheral sympathetic–parasympathetic drives (10). Mindful practice and meditation, both integral to yoga, help in reducing stress (11,12). VVS is a type of reflex syncope mediated by emotional or orthostatic stress and is associated with an increased and imbalanced autonomic activation (13). Recent studies have shown the benefit of yoga in patients with VVS (14,15). This randomized controlled trial (RCT) was conducted to assess the effectiveness of yoga as adjuvant therapy in patients with VVS.
Previous studies have shown reduced cardiovascular risk with increasing high-density lipoprotein cholesterol (HDL-C) levels. However, recent data in the general population have shown increased risk of adverse outcomes at very high concentrations of HDL-C. Thus, we aimed to study the gender-specific relation between very high HDL-C levels (>80, >100 mg/100 ml) and adverse cardiovascular outcomes and the genetic basis in the general population enrolled in the United Kingdom Biobank.
A total of 415,416 participants enrolled in the United Kingdom Biobank without coronary artery disease were included in this prospective cohort study, with a median follow-up of 9 years.
A high HDL-C level >80 mg/100 ml was associated with increased risk of all-cause death (Hazard ratio [HR] 1.11, confidence interval [CI] 1.03 to 1.20, p = 0.005) and cardiovascular death (HR 1.24, CI 1.05 to 1.46, p = 0.01) after adjustment for age, gender, race, body mass index, hypertension, smoking, triglycerides, LDL-C, stroke history, heart attack history, diabetes, eGFR, and frequent alcohol use (defined as ≥3 times/week) using Cox proportional hazard and Fine and Gray's subdistribution hazard models, respectively.
In gender-stratified analyses, such associations were only observed in men (all-cause death HR 1.79, CI 1.59 to 2.02, p <0.0001; cardiovascular death HR 1.92, CI 1.52 to 2.42, p <0.0001), but not in women (all-cause death HR 0.97, CI 0.88 to 1.06, p = 0.50; cardiovascular death HR 1.04, CI 0.83 to 1.31, p = 0.70). The findings persisted after adjusting for the genetic risk score comprised of known HDL-C–associated single nucleotide polymorphisms.
Very high HDL-C levels are associated with an increased risk of all-cause death and cardiovascular death among men but not in women in the general population free of coronary artery disease.
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