Vedin Ola, Lam Carolyn S P, Koh Angela S, Benson Lina, Teng Tiew Hwa Katherine, Tay Wan Ting, Braun Oscar Ö, Savarese Gianluigi, Dahlström Ulf, Lund Lars H
From the Department of Medical Sciences, Uppsala University and Uppsala Clinical Research Center, Sweden (O.V.); National Heart Centre Singapore (C.S.P.L., A.S.K., T.H.K.T., W.T.T.); Duke-NUS Medical School, Singapore (C.S.P.L., A.S.K.); Regional Cancer Centre Stockholm Gotland, Sweden (L.B.); School of Population Health, University of Western Australia, Perth (T.H.K.T.); Department of Cardiology, Skåne University Hospital, Lund University, Sweden (O.Ö.B.); Department of Medicine, Karolinska Institutet, Stockholm, Sweden (G.S., L.H.L.); Department of Cardiology, Karolinska University Hospital, Stockholm, Sweden (G.S., L.H.L.); and Department of Cardiology (U.D.) and Department of Medical and Health Sciences (U.D.), Linkoping University, Sweden.
Circ Heart Fail. 2017 Jun;10(6). doi: 10.1161/CIRCHEARTFAILURE.117.003875.
The pathogenic role of ischemic heart disease (IHD) in heart failure (HF) with reduced ejection fraction (HFrEF; EF <40%) is well established, but its pathogenic and prognostic significance in HF with midrange (HFmrEF; EF 40%-50%) and preserved EF (HFpEF; EF ≥50%) has been much less explored.
We evaluated 42 987 patients from the Swedish Heart Failure Registry with respect to baseline IHD, outcomes (IHD, HF, cardiovascular events, and all-cause death), and EF change during a median follow-up of 2.2 years. Overall, 23% had HFpEF (52% IHD), 21% had HFmrEF (61% IHD), and 55% had HFrEF (60% IHD). After multivariable adjustment, associations with baseline IHD were similar for HFmrEF and HFrEF and lower in HFpEF (risk ratio, 0.91 [0.89-0.93] versus HFmrEF and risk ratio, 0.90 [0.88-0.92] versus HFrEF). The adjusted risk of IHD events was similar for HFmrEF versus HFrEF and lower in HFpEF (hazard ratio, 0.89 [0.84-0.95] versus HFmrEF and hazard ratio, 0.84 [0.80-0.90] versus HFrEF). After adjustment, prevalent IHD was associated with increased risk of IHD events and all other outcomes in all EF categories except all-cause mortality in HFpEF. Those with IHD, particularly new IHD events, were also more likely to change to a lower EF category and less likely to change to a higher EF category over time.
HFmrEF resembled HFrEF rather than HFpEF with regard to both a higher prevalence of IHD and a greater risk of new IHD events. Established IHD was an important prognostic factor across all HF types.
缺血性心脏病(IHD)在射血分数降低的心力衰竭(HFrEF;EF<40%)中的致病作用已得到充分证实,但其在射血分数中等范围(HFmrEF;EF 40%-50%)和射血分数保留(HFpEF;EF≥50%)的心力衰竭中的致病及预后意义则较少被探讨。
我们对瑞典心力衰竭登记处的42987例患者进行了评估,内容包括基线IHD、结局(IHD、心力衰竭、心血管事件和全因死亡)以及在中位随访2.2年期间的EF变化。总体而言,23%患有HFpEF(52%患有IHD),21%患有HFmrEF(61%患有IHD),55%患有HFrEF(60%患有IHD)。经过多变量调整后,HFmrEF和HFrEF与基线IHD的关联相似,而在HFpEF中则较低(风险比,与HFmrEF相比为0.91[0.89-0.93],与HFrEF相比为0.90[0.88-0.92])。HFmrEF与HFrEF发生IHD事件的调整后风险相似,而在HFpEF中较低(风险比,与HFmrEF相比为0.89[0.84-0.95],与HFrEF相比为0.84[0.80-0.9])。调整后,除HFpEF的全因死亡率外,所有EF类别中,现患IHD均与IHD事件及所有其他结局的风险增加相关。随着时间推移,患有IHD的患者,尤其是新发IHD事件的患者,也更有可能转变为较低EF类别,而转变为较高EF类别的可能性较小。
在IHD患病率较高和新发IHD事件风险较大方面,HFmrEF与HFrEF相似,而非与HFpEF相似。已确诊的IHD是所有心力衰竭类型的重要预后因素。