Plasma leptin level is associated with cardiac autonomic dysfunction in patients with type 2 diabetes: HSCAA study

It has been shown that visceral fat accumulation is associated with autonomic dysfunction, though the precise mechanism remains unclear. A recent basic study found that leptin can directly modulate autonomic function through the dorsomedial hypothalamus in relation to obesity. Here, we investigated...

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Veröffentlicht in:Cardiovascular Diabetology 2015-09, Vol.14 (1), p.117-117, Article 117
Hauptverfasser: Kurajoh, Masafumi, Koyama, Hidenori, Kadoya, Manabu, Naka, Mariko, Miyoshi, Akio, Kanzaki, Akinori, Kakutani-Hatayama, Miki, Okazaki, Hirokazu, Shoji, Takuhito, Moriwaki, Yuji, Yamamoto, Tetsuya, Emoto, Masanori, Inaba, Masaaki, Namba, Mitsuyoshi
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container_end_page 117
container_issue 1
container_start_page 117
container_title Cardiovascular Diabetology
container_volume 14
creator Kurajoh, Masafumi
Koyama, Hidenori
Kadoya, Manabu
Naka, Mariko
Miyoshi, Akio
Kanzaki, Akinori
Kakutani-Hatayama, Miki
Okazaki, Hirokazu
Shoji, Takuhito
Moriwaki, Yuji
Yamamoto, Tetsuya
Emoto, Masanori
Inaba, Masaaki
Namba, Mitsuyoshi
description It has been shown that visceral fat accumulation is associated with autonomic dysfunction, though the precise mechanism remains unclear. A recent basic study found that leptin can directly modulate autonomic function through the dorsomedial hypothalamus in relation to obesity. Here, we investigated the mutual relationships among plasma leptin, visceral fat accumulation, and cardiac autonomic dysfunction in patients with type 2 diabetes. This cross-sectional study included 100 diabetic patients, and 100 age- and gender-matched non-diabetic patients with cardiovascular risk factors. Plasma leptin and soluble leptin receptor levels, visceral fat area (VFA), and heart rate variability (HRV) were determined in addition to classical cardiovascular risk factors. In the type 2 diabetic patients, VFA was significantly (p < 0.05) and inversely associated with HRV parameters (SDNN: r = -0.243; SDANN5: r = -0.238), while the plasma level of leptin, but not soluble leptin receptor, was also significantly (p < 0.05) and inversely associated with HRV parameters (SDNN: r = -0.243; SDANN5: r = -0.231). Multiple regression analysis showed that plasma leptin was significantly associated with SDNN and SDANN5 independent of other factors, including age, gender, presence of hypertension and dyslipidemia, duration of diabetes, HbA1c, and eGFR. Furthermore, the relationship of leptin with SDNN and SDANN5 (β = -0.279 and -0.254, respectively) remained significant (p < 0.05) after adjustment for VFA. In patients without diabetes, no significant associations were observed between leptin and any of the HRV parameters. Hyperleptinemia may be involved in cardiac autonomic dysfunction in patients with type 2 diabetes and visceral obesity.
doi_str_mv 10.1186/s12933-015-0280-6
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A recent basic study found that leptin can directly modulate autonomic function through the dorsomedial hypothalamus in relation to obesity. Here, we investigated the mutual relationships among plasma leptin, visceral fat accumulation, and cardiac autonomic dysfunction in patients with type 2 diabetes. This cross-sectional study included 100 diabetic patients, and 100 age- and gender-matched non-diabetic patients with cardiovascular risk factors. Plasma leptin and soluble leptin receptor levels, visceral fat area (VFA), and heart rate variability (HRV) were determined in addition to classical cardiovascular risk factors. In the type 2 diabetic patients, VFA was significantly (p &lt; 0.05) and inversely associated with HRV parameters (SDNN: r = -0.243; SDANN5: r = -0.238), while the plasma level of leptin, but not soluble leptin receptor, was also significantly (p &lt; 0.05) and inversely associated with HRV parameters (SDNN: r = -0.243; SDANN5: r = -0.231). Multiple regression analysis showed that plasma leptin was significantly associated with SDNN and SDANN5 independent of other factors, including age, gender, presence of hypertension and dyslipidemia, duration of diabetes, HbA1c, and eGFR. Furthermore, the relationship of leptin with SDNN and SDANN5 (β = -0.279 and -0.254, respectively) remained significant (p &lt; 0.05) after adjustment for VFA. In patients without diabetes, no significant associations were observed between leptin and any of the HRV parameters. 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Koyama, Hidenori ; Kadoya, Manabu ; Naka, Mariko ; Miyoshi, Akio ; Kanzaki, Akinori ; Kakutani-Hatayama, Miki ; Okazaki, Hirokazu ; Shoji, Takuhito ; Moriwaki, Yuji ; Yamamoto, Tetsuya ; Emoto, Masanori ; Inaba, Masaaki ; Namba, Mitsuyoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c494t-638cd29a0b852f8e72f846944bd58410da8ff1efd363d1eb4e1ed812beaca4d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adiposity</topic><topic>Aged</topic><topic>Analysis</topic><topic>Autonomic Nervous System - physiopathology</topic><topic>Biomarkers - blood</topic><topic>Care and treatment</topic><topic>Case-Control Studies</topic><topic>Chi-Square Distribution</topic><topic>Complications and side effects</topic><topic>Cross-Sectional Studies</topic><topic>Diabetes Mellitus, Type 2 - blood</topic><topic>Diabetes Mellitus, Type 2 - complications</topic><topic>Diabetes Mellitus, Type 2 - diagnosis</topic><topic>Diabetes Mellitus, Type 2 - physiopathology</topic><topic>Female</topic><topic>Glycosylated hemoglobin</topic><topic>Health aspects</topic><topic>Heart - innervation</topic><topic>Heart Diseases - blood</topic><topic>Heart Diseases - diagnosis</topic><topic>Heart Diseases - etiology</topic><topic>Heart Diseases - physiopathology</topic><topic>Heart Rate</topic><topic>Humans</topic><topic>Hypertension</topic><topic>Intra-Abdominal Fat - metabolism</topic><topic>Intra-Abdominal Fat - physiopathology</topic><topic>Leptin</topic><topic>Leptin - blood</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Obesity - blood</topic><topic>Obesity - complications</topic><topic>Obesity - diagnosis</topic><topic>Obesity - physiopathology</topic><topic>Original Investigation</topic><topic>Receptors, Leptin - blood</topic><topic>Risk Factors</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kurajoh, Masafumi</creatorcontrib><creatorcontrib>Koyama, Hidenori</creatorcontrib><creatorcontrib>Kadoya, Manabu</creatorcontrib><creatorcontrib>Naka, Mariko</creatorcontrib><creatorcontrib>Miyoshi, Akio</creatorcontrib><creatorcontrib>Kanzaki, Akinori</creatorcontrib><creatorcontrib>Kakutani-Hatayama, Miki</creatorcontrib><creatorcontrib>Okazaki, Hirokazu</creatorcontrib><creatorcontrib>Shoji, Takuhito</creatorcontrib><creatorcontrib>Moriwaki, Yuji</creatorcontrib><creatorcontrib>Yamamoto, Tetsuya</creatorcontrib><creatorcontrib>Emoto, Masanori</creatorcontrib><creatorcontrib>Inaba, Masaaki</creatorcontrib><creatorcontrib>Namba, Mitsuyoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Health &amp; 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A recent basic study found that leptin can directly modulate autonomic function through the dorsomedial hypothalamus in relation to obesity. Here, we investigated the mutual relationships among plasma leptin, visceral fat accumulation, and cardiac autonomic dysfunction in patients with type 2 diabetes. This cross-sectional study included 100 diabetic patients, and 100 age- and gender-matched non-diabetic patients with cardiovascular risk factors. Plasma leptin and soluble leptin receptor levels, visceral fat area (VFA), and heart rate variability (HRV) were determined in addition to classical cardiovascular risk factors. In the type 2 diabetic patients, VFA was significantly (p &lt; 0.05) and inversely associated with HRV parameters (SDNN: r = -0.243; SDANN5: r = -0.238), while the plasma level of leptin, but not soluble leptin receptor, was also significantly (p &lt; 0.05) and inversely associated with HRV parameters (SDNN: r = -0.243; SDANN5: r = -0.231). Multiple regression analysis showed that plasma leptin was significantly associated with SDNN and SDANN5 independent of other factors, including age, gender, presence of hypertension and dyslipidemia, duration of diabetes, HbA1c, and eGFR. Furthermore, the relationship of leptin with SDNN and SDANN5 (β = -0.279 and -0.254, respectively) remained significant (p &lt; 0.05) after adjustment for VFA. In patients without diabetes, no significant associations were observed between leptin and any of the HRV parameters. Hyperleptinemia may be involved in cardiac autonomic dysfunction in patients with type 2 diabetes and visceral obesity.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>26338087</pmid><doi>10.1186/s12933-015-0280-6</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Adiposity
Aged
Analysis
Autonomic Nervous System - physiopathology
Biomarkers - blood
Care and treatment
Case-Control Studies
Chi-Square Distribution
Complications and side effects
Cross-Sectional Studies
Diabetes Mellitus, Type 2 - blood
Diabetes Mellitus, Type 2 - complications
Diabetes Mellitus, Type 2 - diagnosis
Diabetes Mellitus, Type 2 - physiopathology
Female
Glycosylated hemoglobin
Health aspects
Heart - innervation
Heart Diseases - blood
Heart Diseases - diagnosis
Heart Diseases - etiology
Heart Diseases - physiopathology
Heart Rate
Humans
Hypertension
Intra-Abdominal Fat - metabolism
Intra-Abdominal Fat - physiopathology
Leptin
Leptin - blood
Male
Middle Aged
Multivariate Analysis
Obesity - blood
Obesity - complications
Obesity - diagnosis
Obesity - physiopathology
Original Investigation
Receptors, Leptin - blood
Risk Factors
Up-Regulation
title Plasma leptin level is associated with cardiac autonomic dysfunction in patients with type 2 diabetes: HSCAA study
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