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Published on: December 14, 2011
Gender difference in clinical and genetic characteristics of Brugada syndrome: SADS-TW BrS registry
C-Y J Chen1, J-M J Juang1, L-Y Lin1
1Cardiovascular Center and Division of Cardiology, Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Insights
Brugada syndrome (BrS) shows gender differences. Females experience syncope earlier and have longer QTc intervals, while males with sudden cardiac death (SCD) have longer QRS duration and QTc. SCN5A mutation rates were similar between genders.
Area of Science:
- Cardiology
- Genetics
- Clinical Medicine
Background:
- Brugada syndrome (BrS) is an inherited condition causing sudden cardiac death (SCD), predominantly affecting males.
- Limited data exists on gender-specific differences in BrS.
Purpose of the Study:
- To investigate gender disparities in Brugada syndrome among the Han Chinese population.
- To compare clinical characteristics, electrocardiographic parameters, and SCN5A mutation status between male and female BrS patients.
Main Methods:
- A cohort of 169 Han Chinese BrS patients (153 males, 16 females) in Taiwan was studied between 1998 and 2017.
- Comparative analysis of clinical data, ECG parameters (QTc, QRS duration, PR interval, heart rate), and SCN5A mutation status between genders.
Main Results:
- Females presented with a trend towards higher family history of SCD (31.3% vs. 15%) and significantly longer QTc intervals (457.8 ± 33.0 ms vs. 429.5 ± 42.1 ms).
- Females experienced their first cardiac events (SCD or syncope) at an earlier age than males (P=0.049), primarily due to syncope.
- Males with SCD showed longer QRS duration (114.2 ± 26.8 ms vs. 104.8 ± 15.3 ms) and QTc (442.5 ± 57.4 ms vs. 422.9 ± 28.8 ms). Males with syncope had longer PR intervals (181.2 ± 33.7 ms vs. 165.7 ± 27.1 ms).
Conclusions:
- Significant gender differences exist in Brugada syndrome presentation and risk factors.
- Females with BrS exhibit longer QTc and earlier onset of syncope. Males with SCD are associated with broader QRS and longer QTc, while syncope risk in males is linked to longer PR intervals.
- No significant difference in SCN5A mutation prevalence was observed between genders, suggesting other factors contribute to gender-specific BrS manifestations.
Background:
Brugada syndrome (BrS) is a heritable sudden cardiac death (SCD) disease with male predominance. Information on gender difference of BrS remains scarce.
Aim:
To investigate the gender difference of BrS in Han Chinese.
Design:
We consecutively enrolled 169 BrS patients (153 males and 16 females) from Han Chinese in Taiwan from 1998 to 2017.
Methods:
Clinical characteristics, electrocardiographic parameters and SCN5A mutation status were compared between genders.
Results:
The percentage of family history of SCD in females was slightly higher (31.3% vs. 15%, P = 0.15). Females exhibited longer QTc (457.8 ± 33.0 vs. 429.5 ± 42.1 ms, P < 0.01). Regarding cumulative event occurrence by age, Mantel-Cox test showed females had earlier age of onset of first cardiac events (SCD or syncope) than males (P = 0.049), which was mainly attributed to syncope (P < 0.01). Males with SCD exhibited longer QRS duration (114.2 ± 26.8 vs. 104.8 ± 15.3 ms, P = 0.02) and QTc (442.5 ± 57.4 vs. 422.9 ± 28.8 ms, P = 0.02). Males with syncope exhibited longer PR interval (181.2 ± 33.7 vs. 165.7 ± 27.1 ms, P = 0.01), whereas females with SCD or syncope had a trend towards slower heart rates (69.1 ± 9.6 vs. 82.2 ± 16.3 bpm, P = 0.10) than female with no or mild symptoms. There was no difference in the percentage of SCN5A mutation between genders.
Conclusion:
Gender difference is present in BrS. Females have longer QTc and suffer from syncope earlier than males. Risk of SCD in males is associated with boarder QRS complex and longer QTc, whereas risk of syncope is associated with longer PR interval in males and slower heart rate in females.
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