Gender-dependent association of diabetes mellitus with mortality in patients undergoing transcatheter aortic valve replacement.


Journal

Clinical research in cardiology : official journal of the German Cardiac Society
ISSN: 1861-0692
Titre abrégé: Clin Res Cardiol
Pays: Germany
ID NLM: 101264123

Informations de publication

Date de publication:
Jan 2019
Historique:
received: 23 04 2018
accepted: 18 06 2018
pubmed: 27 6 2018
medline: 24 4 2019
entrez: 27 6 2018
Statut: ppublish

Résumé

Diabetes mellitus (DM) is a risk factor for cardiovascular disease. However, its effect on procedural and follow-up performance after transcatheter aortic valve replacement (TAVR) remains controversial. We performed an observational study of all consecutive patients treated with a transfemoral TAVR in a single-center cohort (n = 1818). All patients were stratified by diabetes status and gender. All-cause 3-year mortality was the primary endpoint. Male patients with DM were identified to have substantially increased 3-year mortality [125/314 (39.8%)] compared to males without DM [142/478 (29.7%), p < 0.01]. Male patients with DM had significantly higher 3-year mortality in comparison to female patients with (p < 0.01) or without DM (p < 0.01). There was no difference in 3-year mortality for female patients with [135/465 (29.0%)] and without DM [151/554 (27.3%); p = 0.70]. This increase in mortality in male DM patients was triggered by both cardiovascular and non-cardiovascular mortality. Furthermore, DM served as an independent predictor of 3-year mortality after TAVR selectively only in men. The interaction between male gender and diabetes mellitus was identified as an independent predictor of 3-year mortality [HR 1.88 (1.25; 2.82); p < 0.01]. DM did not affect 30-day mortality for the overall cohort and for males. Males with DM are a high-risk subgroup of patients after TAVR and require close medical attention including aggressive therapy of modifiable risk factors. Intensified diabetes management may improve long-term survival after TAVR.

Sections du résumé

BACKGROUND BACKGROUND
Diabetes mellitus (DM) is a risk factor for cardiovascular disease. However, its effect on procedural and follow-up performance after transcatheter aortic valve replacement (TAVR) remains controversial.
METHODS AND RESULTS RESULTS
We performed an observational study of all consecutive patients treated with a transfemoral TAVR in a single-center cohort (n = 1818). All patients were stratified by diabetes status and gender. All-cause 3-year mortality was the primary endpoint. Male patients with DM were identified to have substantially increased 3-year mortality [125/314 (39.8%)] compared to males without DM [142/478 (29.7%), p < 0.01]. Male patients with DM had significantly higher 3-year mortality in comparison to female patients with (p < 0.01) or without DM (p < 0.01). There was no difference in 3-year mortality for female patients with [135/465 (29.0%)] and without DM [151/554 (27.3%); p = 0.70]. This increase in mortality in male DM patients was triggered by both cardiovascular and non-cardiovascular mortality. Furthermore, DM served as an independent predictor of 3-year mortality after TAVR selectively only in men. The interaction between male gender and diabetes mellitus was identified as an independent predictor of 3-year mortality [HR 1.88 (1.25; 2.82); p < 0.01]. DM did not affect 30-day mortality for the overall cohort and for males.
CONCLUSION CONCLUSIONS
Males with DM are a high-risk subgroup of patients after TAVR and require close medical attention including aggressive therapy of modifiable risk factors. Intensified diabetes management may improve long-term survival after TAVR.

Identifiants

pubmed: 29943273
doi: 10.1007/s00392-018-1309-0
pii: 10.1007/s00392-018-1309-0
doi:

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

39-47

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Auteurs

Axel Linke (A)

Department of Internal Medicine and Cardiology, Heart Center Dresden, Technical University of Dresden, Fetscherstr. 76, 01307, Dresden, Germany.

Florian Schlotter (F)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University Hospital, Leipzig, Germany.

Stephan Haussig (S)

Department of Internal Medicine and Cardiology, Heart Center Dresden, Technical University of Dresden, Fetscherstr. 76, 01307, Dresden, Germany.

Felix J Woitek (FJ)

Department of Internal Medicine and Cardiology, Heart Center Dresden, Technical University of Dresden, Fetscherstr. 76, 01307, Dresden, Germany.

Georg Stachel (G)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University Hospital, Leipzig, Germany.

Jennifer Adam (J)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University Hospital, Leipzig, Germany.

Robert Höllriegel (R)

Department of Internal Medicine and Cardiology, Heart Center Dresden, Technical University of Dresden, Fetscherstr. 76, 01307, Dresden, Germany.

Anna Lindner (A)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University Hospital, Leipzig, Germany.

Friedrich W Mohr (FW)

Leipzig Heart Institute, Leipzig, Germany.

Gerhard Schuler (G)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University Hospital, Leipzig, Germany.

Philipp Kiefer (P)

Department of Cardiac Surgery, Heart Center Leipzig, University Hospital, Leipzig, Germany.

Sergey Leontyev (S)

Department of Cardiac Surgery, Heart Center Leipzig, University Hospital, Leipzig, Germany.

Holger Thiele (H)

Department of Internal Medicine/Cardiology, Heart Center Leipzig, University Hospital, Leipzig, Germany.

Michael A Borger (MA)

Department of Cardiac Surgery, Heart Center Leipzig, University Hospital, Leipzig, Germany.

David Holzhey (D)

Department of Cardiac Surgery, Heart Center Leipzig, University Hospital, Leipzig, Germany.

Norman Mangner (N)

Department of Internal Medicine and Cardiology, Heart Center Dresden, Technical University of Dresden, Fetscherstr. 76, 01307, Dresden, Germany. norman.mangner@mailbox.tu-dresden.de.

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