Cargando…

Association of peripheral nerve conduction in diabetic neuropathy with subclinical left ventricular systolic dysfunction

BACKGROUND: Subclinical left ventricular (LV) longitudinal myocardial systolic dysfunction occurs in patients with diabetes mellitus (DM) and preserved LV ejection fraction (LVEF), and is closely related to DM-related complications. However, the association of diabetic neuropathy (DN) with subclinic...

Descripción completa

Detalles Bibliográficos
Autores principales: Mochizuki, Yasuhide, Tanaka, Hidekazu, Matsumoto, Kensuke, Sano, Hiroyuki, Toki, Hiromi, Shimoura, Hiroyuki, Ooka, Junichi, Sawa, Takuma, Motoji, Yoshiki, Ryo, Keiko, Hirota, Yushi, Ogawa, Wataru, Hirata, Ken-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428100/
https://www.ncbi.nlm.nih.gov/pubmed/25946999
http://dx.doi.org/10.1186/s12933-015-0213-4
_version_ 1782370838802071552
author Mochizuki, Yasuhide
Tanaka, Hidekazu
Matsumoto, Kensuke
Sano, Hiroyuki
Toki, Hiromi
Shimoura, Hiroyuki
Ooka, Junichi
Sawa, Takuma
Motoji, Yoshiki
Ryo, Keiko
Hirota, Yushi
Ogawa, Wataru
Hirata, Ken-ichi
author_facet Mochizuki, Yasuhide
Tanaka, Hidekazu
Matsumoto, Kensuke
Sano, Hiroyuki
Toki, Hiromi
Shimoura, Hiroyuki
Ooka, Junichi
Sawa, Takuma
Motoji, Yoshiki
Ryo, Keiko
Hirota, Yushi
Ogawa, Wataru
Hirata, Ken-ichi
author_sort Mochizuki, Yasuhide
collection PubMed
description BACKGROUND: Subclinical left ventricular (LV) longitudinal myocardial systolic dysfunction occurs in patients with diabetes mellitus (DM) and preserved LV ejection fraction (LVEF), and is closely related to DM-related complications. However, the association of diabetic neuropathy (DN) with subclinical LV systolic longitudinal dysfunction in such patients has not been fully clarified. METHODS: The subjects of this study were 112 consecutive DM patients with preserved LVEF (all ≥50%) without coronary artery disease and overt heart failure (aged 59 ± 14 years; 60 women, 52 men). Global longitudinal strain (GLS) was determined as the average peak strain of 18 segments from the three standard apical views, and was expressed as an absolute value. DN was diagnosed by experienced diabetologists. Median, ulnar, and sural nerves were subjected to motor and sensory nerve conduction studies. F-wave latency was defined as the minimum F-wave latency after a total of 16 stimulations of the tibial nerve. RESULTS: Forty-one (37%) patients were clinically diagnosed with DN. LV functions of DM patients with and without DN were similar except for GLS being significantly smaller in patients with than in patients without DN (18 ± 2% vs. 20 ± 2%, p < 0.001). It was noteworthy that, of the parameters for the nerve conduction study, only F-wave latency correlated with GLS (r = −0.34, p < 0.001), and also was identified as an independent determinative value of GLS in a multivariate linear regression model (β = −0.25, p = 0.001) even after adjustment for other closely related GLS factors. CONCLUSIONS: Monitoring of F-wave latency may aid early detection of not only DN but also subclinical LV dysfunction. Joint planning of assessment by diabetologists and cardiologists is therefore advisable for better management of DM patients.
format Online
Article
Text
id pubmed-4428100
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-44281002015-05-13 Association of peripheral nerve conduction in diabetic neuropathy with subclinical left ventricular systolic dysfunction Mochizuki, Yasuhide Tanaka, Hidekazu Matsumoto, Kensuke Sano, Hiroyuki Toki, Hiromi Shimoura, Hiroyuki Ooka, Junichi Sawa, Takuma Motoji, Yoshiki Ryo, Keiko Hirota, Yushi Ogawa, Wataru Hirata, Ken-ichi Cardiovasc Diabetol Original Investigation BACKGROUND: Subclinical left ventricular (LV) longitudinal myocardial systolic dysfunction occurs in patients with diabetes mellitus (DM) and preserved LV ejection fraction (LVEF), and is closely related to DM-related complications. However, the association of diabetic neuropathy (DN) with subclinical LV systolic longitudinal dysfunction in such patients has not been fully clarified. METHODS: The subjects of this study were 112 consecutive DM patients with preserved LVEF (all ≥50%) without coronary artery disease and overt heart failure (aged 59 ± 14 years; 60 women, 52 men). Global longitudinal strain (GLS) was determined as the average peak strain of 18 segments from the three standard apical views, and was expressed as an absolute value. DN was diagnosed by experienced diabetologists. Median, ulnar, and sural nerves were subjected to motor and sensory nerve conduction studies. F-wave latency was defined as the minimum F-wave latency after a total of 16 stimulations of the tibial nerve. RESULTS: Forty-one (37%) patients were clinically diagnosed with DN. LV functions of DM patients with and without DN were similar except for GLS being significantly smaller in patients with than in patients without DN (18 ± 2% vs. 20 ± 2%, p < 0.001). It was noteworthy that, of the parameters for the nerve conduction study, only F-wave latency correlated with GLS (r = −0.34, p < 0.001), and also was identified as an independent determinative value of GLS in a multivariate linear regression model (β = −0.25, p = 0.001) even after adjustment for other closely related GLS factors. CONCLUSIONS: Monitoring of F-wave latency may aid early detection of not only DN but also subclinical LV dysfunction. Joint planning of assessment by diabetologists and cardiologists is therefore advisable for better management of DM patients. BioMed Central 2015-05-07 /pmc/articles/PMC4428100/ /pubmed/25946999 http://dx.doi.org/10.1186/s12933-015-0213-4 Text en © Mochizuki et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Investigation
Mochizuki, Yasuhide
Tanaka, Hidekazu
Matsumoto, Kensuke
Sano, Hiroyuki
Toki, Hiromi
Shimoura, Hiroyuki
Ooka, Junichi
Sawa, Takuma
Motoji, Yoshiki
Ryo, Keiko
Hirota, Yushi
Ogawa, Wataru
Hirata, Ken-ichi
Association of peripheral nerve conduction in diabetic neuropathy with subclinical left ventricular systolic dysfunction
title Association of peripheral nerve conduction in diabetic neuropathy with subclinical left ventricular systolic dysfunction
title_full Association of peripheral nerve conduction in diabetic neuropathy with subclinical left ventricular systolic dysfunction
title_fullStr Association of peripheral nerve conduction in diabetic neuropathy with subclinical left ventricular systolic dysfunction
title_full_unstemmed Association of peripheral nerve conduction in diabetic neuropathy with subclinical left ventricular systolic dysfunction
title_short Association of peripheral nerve conduction in diabetic neuropathy with subclinical left ventricular systolic dysfunction
title_sort association of peripheral nerve conduction in diabetic neuropathy with subclinical left ventricular systolic dysfunction
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428100/
https://www.ncbi.nlm.nih.gov/pubmed/25946999
http://dx.doi.org/10.1186/s12933-015-0213-4
work_keys_str_mv AT mochizukiyasuhide associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT tanakahidekazu associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT matsumotokensuke associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT sanohiroyuki associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT tokihiromi associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT shimourahiroyuki associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT ookajunichi associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT sawatakuma associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT motojiyoshiki associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT ryokeiko associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT hirotayushi associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT ogawawataru associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction
AT hiratakenichi associationofperipheralnerveconductionindiabeticneuropathywithsubclinicalleftventricularsystolicdysfunction