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The edition · Cardiology

TAVR's quality-of-life lead fades by year three, and SGLT2 inhibitors in early pregnancy look reassuring but unproven

Seven-year PARTNER 3 data reframe the low-risk valve conversation; a small meta-analysis addresses inadvertent SGLT2 inhibitor exposure in pregnancy; and a common CD36 variant outweighs titin in African-ancestry dilated cardiomyopathy.

The edition in brief

In 943 low-risk PARTNER 3 patients, both transcatheter and surgical aortic valve replacement produced lasting gains in Kansas City Cardiomyopathy Questionnaire scores through seven years. TAVR led by 16.2 points at one month and 1.9 points at two years, with no difference from year three; about 60% in each arm had an excellent outcome at seven years. A meta-analysis of three cohorts (669 exposed pregnancies) found no association between early SGLT2 inhibitor exposure and major congenital malformations versus insulin (RR 0.94, 0.68–1.29), but the intervals are wide and one cohort raised a possible heart-defect signal with exposure in weeks 4–10. In 82,623 people of African ancestry, the CD36 Y325* nonsense variant carried an OR of 4.8 for dilated cardiomyopathy in homozygotes and a population attributable fraction of 9.0%, above titin truncating variants at 3.7%. A meta-analysis of small trials suggested adding a PCSK9 inhibitor to statin after acute ischaemic stroke improved functional independence, with low to moderate certainty. A HELIOS-B analysis found vutrisiran's benefit in transthyretin cardiomyopathy was not modified by tafamidis or heart failure drugs. The pearl covers contraception counselling when prescribing SGLT2 inhibitors to women of reproductive age.

In this edition
01
Clinical update

SGLT2 inhibitors in early pregnancy: no clear malformation signal, but too little data to reassure

Discuss contraception when prescribing an SGLT2 inhibitor to a woman of reproductive age, and stop it once pregnancy is confirmed.

2 min · EndocrineRead →
Primary outcome
Major congenital malformations versus insulin
Effect
RR 0.94 (95% CI 0.68–1.29); cardiac malformations RR 0.97 (0.64–1.48)
02Research

A common CD36 variant explains more African-ancestry dilated cardiomyopathy than titin

In African-ancestry dilated cardiomyopathy, ask whether the gene panel covers CD36 before calling it non-genetic.

1 min · JAMARead →
03Research

PCSK9 inhibitor plus statin after ischaemic stroke: an early signal from small trials

Keep to statin, then ezetimibe, then PCSK9 inhibitor after ischaemic stroke; do not start one acutely on this evidence.

1 min · Journal of neurologyRead →
04Research

Vutrisiran's benefit in ATTR cardiomyopathy holds with tafamidis and heart failure drugs

Vutrisiran's benefit in ATTR cardiomyopathy appears consistent whether or not patients take tafamidis or heart failure drugs.

1 min · Journal of the American College of CardiologyRead →
05Pearl

The contraception question when starting cardiometabolic drugs

Raise contraception when you prescribe, not after a positive pregnancy test.

1 minRead →
06
Practice changer

TAVR or surgery at low risk: quality of life converges by year three

At low surgical risk, present TAVR's advantage as faster recovery; long-term quality of life is similar with either valve.

2 min · Journal of the American College of CardiologyRead →
Primary outcome
KCCQ overall summary score over time
Effect
+16.2 points at 1 month (14.3–18.1); +1.9 at 2 years (0.2–3.7); no difference years 3–7

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