Key result
Time with nocturnal SpO2 < 90% exceeding 30 minutes independently predicted major adverse cardiac events in patients with cardiac amyloidosis (P=0.005).
Why the study?
Does sleep-disordered breathing predict major adverse cardiac events in patients with cardiac amyloidosis?
Observational (n=70)
Does sleep-disordered breathing predict major adverse cardiac events in patients with cardiac amyloidosis?
Answers are grounded in this paper and cite their sources.
Nocturnal hypoxemia may stratify MACE risk in cardiac amyloidosis; leaves open whether SDB treatment improves outcomes.
STUDY OBJECTIVES: To assess prevalence, severity, and prognostic value of sleep-disordered breathing (SDB), in the three main cardiac amyloidosis (CA) types, i.e., light-chain (AL), transthyretin-related familial (m-TTR), or senile (WT-TTR). METHODS: Patients consecutively referred for CA diagnosis work-up underwent cardiac assessment and nocturnal polygraphy. SDB was defined as apnea-hypopnea index (AHI) ≥ 5/h. Multivariate analysis was used to identify predictors of a major adverse cardiac event (MACE) defined as death, heart transplantation and acute heart failure. RESULTS: Seventy CA patients were included (31 AL, 22 m-TTR, 17 WT-TTR). The mean ± standard deviation age and left ventricular ejection fraction were 71 ± 12 years and 49% ± 13% and median (interquartile range) N terminal pro brain natriuretic peptide (NT-proBNP) was 3,932 (1,607; 7,028) pg/mL. The prevalence of SDB was 90% without difference between amyloidosis types. SDB was central in 27% and obstructive in 73%. AL had less frequent severe SDB compared to m-TTR and WT-TTR (P = 0.015) but longer time with peripheral capillary oxygen saturation (SpO2) < 90% (P = 0.037). After a median follow-up of 7.5 (2.8; 14.9) months, 49% patients experienced MACE. Time with nocturnal SpO2 < 90% was the only independent predictor of MACE. The best-identified threshold was 30 min. Values > 30 min were associated with bad prognosis (Log-rank χ(2): 8.01, P value = 0.005). Using binomial logistic regression, determinants of time with nocturnal SpO2 < 90% were New York Heart Association class (P = 0.011), and log-NT-proBNP (P = 0.04) but not AHI. CONCLUSIONS: In CA population, prevalence of SDB is high (90%) and dominated by the obstructive pattern. Bad prognosis in this population was driven by nocturnal desaturation, reflecting heart failure severity and respiratory involvement.
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Bodez et al. (2016) conducted an observational in Cardiac amyloidosis (n=70). Nocturnal polygraphy was evaluated on Major adverse cardiac event (MACE) defined as death, heart transplantation and acute heart failure (p=0.005). Time with nocturnal SpO2 < 90% exceeding 30 minutes independently predicted major adverse cardiac events in patients with cardiac amyloidosis (P=0.005).
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