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Hyperinsulinemia correlates with low levels of plasma B-type natriuretic peptide in Japanese men irrespective of fat distribution
Cardiovascular Diabetology volume 11, Article number: 22 (2012)
B-type natriuretic peptide (BNP), a member of the natriuretic peptide family, is a cardiac-derived secretory hormone with natriuretic, diuretic, and vasorelaxant activities. Intraabdominal fat accumulation is associated with atherosclerotic cardiovascular diseases and cardiac dysfunction. Circulating BNP levels are relatively low (within the normal limits) in obesity and the metabolic syndrome. However, the relationship between plasma BNP levels and visceral fat accumulation in general population has not been reported. The present study analyzed the relationships between plasma BNP levels and various clinical variables, including insulin, visceral and subcutaneous fat area (VFA and SFA, respectively), in normal Japanese men.
The study (Victor-J study) subjects were consecutive 500 Japanese male workers, who underwent a health checkup and were measured VFA and SFA by computed tomography.
Age-adjusted simple linear regression analysis showed that log-BNP correlated positively with HDL-cholesterol, and negatively with VFA, log-immunoreactive insulin (IRI), log-triglyceride, and LDL-cholesterol, but not body mass index or SFA. Stepwise multiple regression analysis identified log-IRI and HDL-cholesterol as significant determinants of log-BNP. Subjects with IRI ≥5.5 μIU/mL had lower plasma BNP levels than those with IRI < 5.5 μIU/mL, irrespective of obesity (body mass index, cutoff value 25 kg/m2), visceral fat accumulation (VFA, cutoff value 100 cm2) and subcutaneous fat accumulation (SFA, cutoff value 128 cm2).
Our study showed that hyperinsulinemia correlated with low levels of plasma BNP in general men, irrespective of fat distribution.
B-type natriuretic peptide (BNP), a member of the natriuretic peptide (NP) family, is a cardiac-derived secretory hormone with natriuretic, diuretic, and vasorelaxant activities [1, 2]. Plasma BNP level correlates with the severity of heart failure, and is clinically used as a marker of cardiac dysfunction . Evidence suggests that high BNP levels regulate endogenous antagonism of vasoconstriction, the salt- and water-retaining system that acts to prevent a rise in blood pressure, and plasma volume expansion through direct natriuresis, diuresis, and vasodilation.
Visceral fat accumulation correlated closely with systolic blood pressure , and is also related to the development of cardiac dysfunction . However, circulating NPs levels are relatively low (within the normal limits) in obesity [6–11]. It has been suggested that obese subjects have a "natriuretic handicap", with a reduced NPs response to cardiac wall stress. Low NPs levels may contribute to the pathophysiology of cardiac dysfunction in visceral adiposity. The present study analyzed the relationships between plasma BNP levels and various clinical variables, including insulin, visceral and subcutaneous fat area (VFA and SFA, respectively), in normal Japanese men.
The study subjects were consecutive 500 Japanese male employees, who underwent a health checkup in year 2010 at Hitachi Ltd, Ibaraki Prefecture, including computed tomography (CT). The present study was approved by the human ethics committees of the National Center for Global Health and Medicine, Osaka University and Hitachi Health Care Center. Written informed consent was obtained from all subjects. This trial (Victor-J study) is registered with the University Hospital Medical Information Network (#UMIN 000004318)
Anthropometry and laboratory measurements
Height and weight were measured in standing position. Body mass index (BMI) was calculated and expressed in kg/m2. Blood pressure was measured in a sitting position with a standard mercury sphygmomanometer on the right or left arm after the subjects had rested for at least 5 minutes. VFA and SFA were computed and measured automatically using commercial software on a CT scan taken at the umbilical level in supine position [120 kV, 400 mAsec, section thickness of 5-10 mm, field of view of 400 mm, window width of 800- 1,000 Hounsfield units]. Venous blood samples were collected in the morning after overnight fast for measurements of creatinine, hemoglobin A1c (HbA1c), HDL-cholesterol, LDL-cholesterol, triglyceride, glucose, and immunoreactive insulin (IRI). The value for HbA1c (%) is estimated as National Glycohemoglobin Standardization Program (NGSP) equivalent value (%) calculated by the formula HbA1c (%) = HbA1c (Japan Diabetes Society [JDS],%) + 0.4%. Plasma BNP concentrations were measured with specific immunoradiometric assay for human BNP (BNP kit, Shionogi, Osaka, Japan, normal range; < 18.4 pg/mL, intracoefficients of variation (CV); 2.7-9.6%, inter-CV 5.6-11.8%, range [2.0-2,000 pg/mL]).
Data are presented as mean ± SD (Tables) or mean ± SEM (Figure). Stepwise multiple regression analysis was first conducted to identify those parameters that significantly contributed to log-BNP, and parameters with F value > 4.0 were subsequently entered into the regression analysis as independent variables. The subjects were divided into four groups according to; (analysis 1) BMI (cutoff value 25 kg/m2; obesity) and IRI (cutoff value 5.5 μIU/mL; median value), (analysis 2) VFA (cutoff value 100 cm2; visceral fat accumulation) and IRI (cutoff value 5.5 μIU/mL; median value), (analysis 3) SFA (cutoff value 128 cm2; median value) and IRI (cutoff value 5.5 μIU/mL; median value). Differences among groups were compared by one- or two-way analysis of variance (ANOVA) with Fisher's protected least significant difference test for multiple-group analysis or unpaired Student's t-test for experiments involving only two groups. In all cases, p values < 0.05 were considered statistically significant. All analyses were performed with the JMP Statistical Discovery Software 8.0 (SAS Institute, Cary, NC).
Characteristics of subjects enrolled in the present study
The baseline characteristics of the subjects who underwent a health checkup are listed in Table 1. Only 12.4% (n = 62) were hyper-BNPemic (above the normal range; upper limit of normal range; ≥18.4 pg/mL), and 70.2% of the subjects (n = 351) had visceral fat accumulation (VFA ≥100 cm2).
Correlation analysis between plasma BNP levels and measured parameters
Table 2 lists the correlation coefficients for the relationship between BNP and various clinical parameters. Data of BNP showed skewed distribution (Figure 1A), and therefore were log-transformed before analysis. Age-adjusted simple linear regression analysis showed that log-BNP correlated positively with HDL-cholesterol (Figure 1B), and negatively with VFA, log-IRI (Figure 1B), log-triglyceride, and LDL-cholesterol, but not BMI or SFA. Stepwise multiple regression analysis identified HDL-cholesterol and log-IRI as significant and independent determinants of log-BNP.
Comparisons of clinical features including plasma BNP levels according to obesity and fat distribution
Subjects with IRI ≥5.5 μIU/mL had lower plasma BNP levels than those with IRI < 5.5 μIU/mL, irrespective of obesity (analysis 1, Table 3), visceral fat accumulation (analysis 2, Table 4), and subcutaneous fat accumulation (analysis 3, Table 5) (Figure 2). These results suggest that hyperinsulinemia correlates with low levels of plasma BNP, irrespective of fat distribution.
Our cross-sectional study of Japanese male subjects demonstrated for the first time that hyperinsulinemia correlated with low levels of plasma BNP, irrespective of fat distribution. The present study also found that HDL-cholesterol was a significant determinant of log-BNP. Although Wang et al. demonstrated that reduced HDL-cholesterol was associated with lower plasma BNP levels by multivariable analysis , the mechanism remains unclear.
As the mechanisms, we should consider the effect of hyperinsulinemia on BNP production and catabolism. There is controversy on whether or not hyperinsulinemia directly suppresses BNP production [13, 14]. NPs, through the activation of the biologically active membrane guanylate-cyclase-linked NPR-1 has a potent lipolytic effect in human adipocytes via a cGMP-dependent mechanism  and activation of hormone-sensitive lipases [16, 17]. Metabolism of NPs is regulated by two degradative pathways; uptake by the clearance receptor, natriuretic peptide receptor-3 (NPR-3) and hydrolysis by NEP . Our and the other groups previously demonstrated that, 1) NPR-1, NPR-2 and NPR-3 mRNAs are expressed in the adipose tissues, however mRNA level of NEP is relatively low , and 2) lower NPR-1 mRNA levels and higher NPR-3 mRNA levels in the adipose tissues of ob/ob mice  or in the adipose tissues and muscle of diet-induced mice , models of hyperinsulinemia, compared to lean mice. Plasma NEP levels were higher in diet-induced mice and tissue NEP was increased in mesenteric fat in diet-induced mice, compared with normal-diet mice . The effect of insulin on NEP has not been reported. Taken together, dysregulation of two degradative pathways under hyperinsulinemia may be, at least partly, responsible for low circulating BNP levels.
Amino-terminal pro-BNP (NT-proBNP), which is co-secreted in equimolar amounts with BNP from the cardiac ventricle, is also well-established as a diagnostic marker in heart failure [22, 23]. Surgical weight loss with reduced insulin levels was associated with increases in NT-proBNP . Women with gestational diabetes mellitus under insulin therapy had lower circulating NT-proBNP levels than those under medical nutrition therapy or healthy pregnancies . These results suggest that circulating levels of NT-proBNP as well as BNP may be regulated by insulin. However, clearance of plasma NT-proBNP occurred across kidney, liver, musculoskeletal, and head and neck tissue , differ from plasma BNP cleared by NPRs and NEP. Further experimental and clinical studies including both BNP and NT-proBNP are required. Improvement of hyperinsulinemia may reduce plasma volume and thus lower blood pressure through the increase in plasma NPs levels. This may reduce susceptibility for cardiac dysfunction in subjects with hyperinsulinemia.
In conclusion, hyperinsulinemia correlated with low levels of plasma BNP in general men, irrespective of fat distribution.
Several limitations of this study must be considered. First, this is a cross-sectional study, making it difficult to establish a cause-effect relationship. Further prospective studies should be conducted in the future to analyze this relationship. Second, the results may not be applicable to females or non-Japanese populations. Finally, in the present study, drug information was based on information provided by the subjects or their relatives. The current study may include the effects of use of various medications for diabetes, hypertension and dyslipidemia. Further studies that include untreated patients need to be conducted.
B-type natriuretic peptide
Natriuretic peptide receptor
Subcutaneous fat area
Visceral fat area.
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We thank all staff at Hitachi, Ltd. Hitachi Health Care Center for the data collection and technical assistance. This research was supported in part by a Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area) "Molecular Basis and Disorders of Control of Appetite and Fat Accumulation" (#22126008, to T.F. and K.K.).
K.K. and T.F. are members of the "Department of Metabolism and Atherosclerosis", a sponsored course endowed by Kowa Co. Ltd. and a company researcher is dispatched to the course. All other authors declare no competing interests.
HN and KK researched and analyzed data. KK also participated in the concept and design of the study, interpretation of data and reviewed/edited the manuscript. TN recruited the patients and collected the data. TF and IS contributed to discussion and wrote the manuscript. All authors read and approved the final version of the manuscript.
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Nakatsuji, H., Kishida, K., Funahashi, T. et al. Hyperinsulinemia correlates with low levels of plasma B-type natriuretic peptide in Japanese men irrespective of fat distribution. Cardiovasc Diabetol 11, 22 (2012) doi:10.1186/1475-2840-11-22
- B-type natriuretic peptide
- Visceral fat