In PROVE-HF we demonstrated significant reverse cardiac remodeling associated with sac/val therapy during a 12 m treatment period, however the impact on MR remained uncertain.
We therefore sought to examine association between rx with sac/val and changes in MR severity.
Following enrollment, sac/val was initiated and titrated to maximally-tolerated doses.
An echo was performed at baseline, 6 m, and 12 m and read in a core lab in a temporally-blinded fashion.
MR severity was graded consistent with ASE guidelines from 0-4+.
After excluded those missing interpretable MR data or those with prior MV procedures, the baseline data are shown attached.
This was a typical HFrEF population, mean age of 65 years, Class II predominant. About 50% had non-ischemic HFrEF.
76% were taking ACE/ARB at baseline.
The baseline echo data are attached. The median LVEF was 28%, and study participants had significant LA and LV remodeling, along with prevalent diastolic dysfunction.
At baseline 14.9% had 3-4+ MR ("eligible for MV clipping").
The Sankey diagram depicts association between sac/val treatment and change in MR over a 12 m period. Note the shift toward lesser severe MR.
From baseline to 6 m, prevalence of 3-4+ MR decreased by 45%.
This improvement remained consistent at 12 m (44.7%).
We then examined those with 3-4+ MR at baseline to see if one could predict who would "respond" with improved MR versus those who would not.
Why?
Some have suggested that those with MR due to organic valve disease (vs remodeling) might be identifiable early on.
The bottom line is that whether examining either clinical variables or baseline echo variables, it was impossible to identify those with proportionate (due to LV remodeling) and disproportionate (due to valve dx) MR.
Those decreasing MR from 3-4+ had ⬇️NT-proBNP concentrations by 12 months and they had greater improvement in LV remodeling. Lastly, the KCCQ-23 of responders was more significantly improved.
So they had better prognosis, improved LV function and felt better. Win/Win/Win.
PROVE HF was a single arm, observational study, so improvement in MR might have been due to other factors.
Nonetheless, the results of this study are consistent with smaller studies and provide insights into change in MR following initiation of Sac/Val in usual care.
We conclude that among study participants with HFrEF, treatmement with sac/val was associated with a substantial reduction in 3-4+ MR.
This MR reduction was associated with greater reduction in NT-proBNP, improved health status and considerable reverse cardiac remodeling.
Furthermore, baseline clinical and echocardiographic characteristics of those with 3-4+ MR who had a reduction to ≤2+ MR by 12 months were similar to those who did not.
Thus, predicting presence of MR due to LV dz versus intrinsic valve dz without GDMT optimization is difficult
Make no mistake about it, clipping the MV in someone with symptomatic HFrEF optimized on GDMT but with 3-4+ MR is an important consideration. This procedure has doubled in frequency since COAPT.
These results extend the definition of "optimized" GDMT prior to MV procedures.
Prior to proceeding with a MV procedure, our data suggest that "optimized" GDMT should include a treatment course of sacubitril/valsartan.
It is important to recognize the exceptionally hard work of Dr. Alaa Omar and @Jcontreras75 from @MountSinaiHeart, whose Herculean efforts helped make this analysis possible.
A year-end #Tweetorial for #MedTwitter about serial biomarker testing for clinical evaluation of patients with #HeartFailure.
The use of serial #NTproBNP testing, often at every office visit has grown.
New data are available that emphasize the importance. Read on 👇
In a just-published analysis, colleagues from the GUIDE-IT Trial team examined the prognostic meaning of a single versus serial assessment of NT-proBNP among individuals with chronic #HFrEF.
In the trial, study participants had multiple NT-proBNP measurements during a year of follow up (and had adjudicated outcomes), so we asked three basic questions.
Day 6 on service at @MGHHeartHealth and we're running on fumes. But Thanksgiving is just around the corner, so all is well.
At the request of Dr. @CoronaryDoc, a thread on appropriate use of natriuretic peptides.
There's a time to measure them. And a time not to.
Just a reminder of NP biology:
NP genes are highly conserved across species. Your ANP is only one amino acid different than the ANP of a rat, for example.
In addition to being conserved across species, the three CV NPs (ANP, BNP, CNP) have structural similarities.
In addition to having a common ring structure responsible for their biologic effect, all three CV NPs (A, B, C) are synthesized as pre-pro-peptides, and are processed by corin/furin to liberate an N-terminal pro-peptide and a biologically active C-terminal fragment.
Day 5 on service at @MGHHeartHealth. No better time than now to think about the favorite drug of @AndrewJSauer...spironolactone.
The story of how the drug was discovered is interesting, and gave a hint as to the fact the drug would eventually become a pillar of HF care.
The first mineralocorticoid synthesized was deoxycorticosterone (DOC). Simultaneously, aldosterone was discovered. Both exerted powerful sodium retention effects. This was in the early 1950s.
Simultaneously, people began to recognize that pts with HF retained salt and water...
Recognizing that Na/water retention in HF resembled that of DOC/aldo treatment, efforts began on the synthesis of ways to block their effects with a family of compounds called 17-spironolactones.
one had potent anti-mineralocorticoid effects, and was dubbed "aldactone".
One: begin your target BB at the start. I don’t know how the culture of starting short acting metoprolol “for titration” came from but it’s not supported by any science, uses a drug that failed in the MDC trial, and may actually be harder to titrate due to on/off effects.
Two: if you use carvedilol, scan the med list for other alpha blockers and d/c them. Carvedilol has alpha blocking effects, so if you d/c the other it’s likely to “buy” more BP, and won’t be noticed. Remember—tamsulosin (used for BPH) is an alpha blocker…
It's a little known fact that prior to the PH3 PARADIGM trial, a PH2 study in HFrEF was not performed--normally PH2 studies provide target doses for the pivotal outcomes trials.
So how was the dose of sacubitril/valsartan chosen??
The target dose of 97/103 mg twice daily was selected to achieve serum concentrations of valsartan = to those in Val-HeFT and VALIANT while simultaneously achieving 90% neprilysin inhibition in normal individuals.
Thanks to work by @pmyhre in our group, we have some new and interesting data.
A 🧵, read on! 👇
When the #PARADIGM-HF study was published, one of the things immediately noticed was the increase in BNP that occurred after being started on sacubitril/valsartan.
This is because through effect of sacubitril, neprilysin is inhibited. Why might this lead to an increase in BNP?
#Neprilysin is a ubiquitous metalloproteinase that assaults BNP (among other targets including ANP and CNP) and cleaves it in numerous places as shown.
Note that in BNP, there are cleavage sites that involve numerous places where immunoassays for measurement of BNP may bind.