DOI: https://doi.org/10.21203/rs.3.rs-16399/v1
Background Galectin-3 binding protein (GAL-3BP) is one of the major fucosylated glycoprotein family members, and is implicated in nonalcoholic fatty liver disease, lipid dysfunctions and coronary artery disease recently. Here we analyzed the serum concentrations of GAL-3BP in postmenopausal women, to evaluate the association of circulating GAL-3BP and insulin resistance in female after menopause.
Method We evaluated serum levels of Gal-3BP in sixty-two non-diabetic women in menopausal status for at least one year. The clinical features, biochemistry profiles and homeostasis model assessment of insulin resistance (HOMA-IR) were obtained routinely.
Results Gal-3BP levels increased in women with higher HOMA-IR values and was positively correlated to HOMA-IR. It was also an independent risk factors for HOMA-IR and showed the most influence on HOMA-IR comparing to FPG, TG, age and BMI. The cut-off value of serum Gal-3BP level was 2234.3150 ng/ml with the area under the ROC curve (AUC) 0.68 (HOMA-IR 1.5), 0.81 (HOMA-IR 2.0) and 0.93 (HOMA-IR 2.5).
Conclusions Serum levels of Gal-3BP is associated with impaired insulin sensitivity in non-diabetic menopausal women.
Insulin resistance is a complicated condition in which the insulin sensitivity of primary metabolic tissues, including the liver, white adipose tissue and skeletal muscle, is impaired, and insulin resistance is considered to be one of the major causes of type 2 diabetes and cardiovascular diseases. Menopausal women who have ceased menstruating for at least one year have a markedly higher probability of developing insulin resistance than age-matched premenopausal women, with the prevalence most commonly estimated at the level of 31%-55% [1,2]. There is growing evidence indicating that hormone fluctuation triggered by menopause, especially decreasing levels of oestrogen in the circulation, may lead to increased visceral adipose deposition and systemic inflammatory responses, but the underlying mechanism remains unclear in many aspects.
Galectin-3 binding protein (Gal-3BP), one of the major fucosylated glycoprotein family members, appears to be implicated in the immune response and in cytotoxicity [3,4]. Recently, several clinical investigations have suggested that Gal-3BP is related to metabolic dysfunctions ranging from non-alcoholic fatty liver disease to atherosclerosis [5–7]. However, few studies have focused on the relationship between insulin resistance and Gal-3BP, and the results remain controversial [8,9]. For this reason, we conducted this study focused on the associations between Gal-3BP and insulin homeostasis and the relevance of Gal-3BP as a biomarker of insulin resistance in the menopausal population.
2.1 Subjects
Sixty-two women after menopause were recruited from the Physical Examination Centre of the Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine, between January and April 2019. The study was approved by institutional review boards at the Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine.
Exclusion criteria were pre- and peri-menopausal status; acute infection phase; a history of autoimmune, hepatic, renal, malignant tumoral or psychiatric diseases; a history of diabetes or heart stents; and the intake of a female hormone that is known to affect circulating sex steroids within the three months prior to the study.
2.2 Anthropometric evaluation
Participants were invited to the Physical Examination Centre between 8:00 and 10:00 am after overnight fasting. Anthropometric measurements, such as age, weight and height, were collected by trained personnel. BMI was calculated as weight in kilograms divided by height in metres squared. Blood pressure was measured in a resting state.
2.3 Blood sampling and biochemical analysis
Venous blood samples were collected and kept at room temperature for 30 min and then centrifuged at 1500×g and 4 °C for 15 min within 5 h of collection. Biochemical variables such as alanine transaminase (ALT), triglycerides (TG), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), fasting plasma glucose (FPG), and fasting insulin (FINS) were determined according to standard laboratory methods.
Homeostatic model assessment of insulin resistance (HOMA-IR) indices were calculated as follows: HOMA-IR index = fasting glucose (mmol/dl) × fasting insulin (µmol/L)/22.5.
2.4 Measurement of circulating Gal3-BP by ELISA
Serum Gal-3BP levels were measured with an enzyme immunoassay kit according to standard instructions (Human LAGLS3BP ELISA Kit, RayBio Inc.).
All assays were performed in duplicate, and average data were collected.
2.5 Statistical analysis
Statistical Package for the Social Sciences software (SPSS Inc. version 22.0, Armonk, USA) and GraphPad Prism (version 6.0, CA, USA) were used to analyse the data. The Kolmogorov-Smirnov test was used for normality evaluation. Normally distributed data are expressed as the mean ± SD. Data not normally distributed were expressed as the median (25th -75th IQR). Before performing further analyses, non-normally distributed parameters were log-, square-, or normal-score- transformed. One-way ANOVA was performed for multi-group comparisons. The Kruskal-Wallis test was used for non-normally distributed data. Pearson’s correlation analysis was used to determine the correlation of serum Gal-3BP with demographic and biochemical parameters. Multivariate analysis was performed by logistic regression to observe variables influencing the risk for insulin resistance adjusted for age and BMI. The diagnostic performance of Gal-3BP was analysed by receiver operating characteristic (ROC) curves and the area under the ROC curve (AUC). The Youden index was used to identify the optimal cut-off points. Probability values were 2 tailed, and a p value <0.05 was considered significant.
3.1 Clinical, metabolic and hormonal features of the study population.
The parameters of clinical and biochemistry were given in four subgroups according to the quartiles of the HOMA-IR index, as shown in Table 1 and Fig. 1. Age, BMI, SBP, DBP, and circulating levels of FPG, FINS and ALT were significantly different among the four subgroups, while SBP and serum levels of TC, TG, HDL-C, and LDL-C were similar. Moreover, serum levels of Gal-3BP in the fourth quartile of HOMA-IR index subgroups were significantly higher than those of lower HOMA-IR index quartiles (p <0.05).
3.2 Association between Gal-3BP concentrations and metabolic parameters.
We performed Pearson’s correlation test in all subjects. The results showed that serum Gal-3BP levels were positively associated with fasting insulin (r=0.517, p=0.000) and the HOMA-IR index (r=0.513, p=0.000). There was a significant linear increase in Gal-3BP expression with increasing quartiles of the HOMA-IR index. The data are summarized in Table 2 and Fig. 2.
3.3 The influence of serum Gal-3BP levels on the HOMA-IR index in women after menopause.
Multiple linear regression analysis showed that Gal-3BP, FPG, TG, age and BMI were independent risk factors for a high HOMA-IR index. Serum levels of Gal-3BP showed the most influence on the HOMA-IR index. The data are listed in Table 3.
3.4 Ability of serum Gal-3BP levels to distinguish insulin-resistant individuals from all subjects.
We investigated the ability of serum Gal-3BP levels to distinguish insulin-resistant patients from all individuals using the ROC curve shown in Table 4 and Fig. 3. Since there was great variability in the optimal reference range of the HOMA-IR index, we obtained three cut-off values, including 1.5, 2.0, and 2.5, as suggested by several studies [10-15]. The cut-off value of Gal-3BP was 2234.3150 ng/ml.
The present work focused on the expression of Gal-3BP in non-diabetic menopausal women. Our results consistently indicated that a higher level of Gal-3BP was associated with increased insulin resistance. This finding was in line with data from previous in vivo and in vitro studies that showed increased expression of Gal-3BP in different phenotypes of metabolic syndrome, including non-alcoholic fatty liver disease, obesity and silent atherosclerosis [16,17]. However, in contrast to some previous studies, our data failed to show a significant correlation between Gal-3BP and clinical lipid profiles or age in women after menopause [9,18]. This may be due to differences in study subjects owing to the selective inclusive criteria and may imply that Gal-3BP is more associated with adipose dysfunction than with fat deposition [19].
Multiple linear regression analysis showed that Gal-3BP was an independent and significant determinant for impaired insulin sensitivity. Furthermore, Gal-3BP non-invasively and reliably predicted insulin sensitivity on the basis of the several tested HOMA-IR index cut-off values in our study. Considering that circulating Gal-3BP increased when insulin dynamics were impaired much earlier than clinical diabetes diagnosis was confirmed, it is plausible that Gal-3BP is associated with the onset of insulin resistance and has an impact on the pathogenesis of type 2 diabetes mellitus.
As a binding protein, Gal-3BP binds specifically to human macrophage-associated lectins and is implicated in the immune response associated with natural killer (NK) and lymphokine-activated killer (LAK) cell cytotoxicity. Gal-3BP is suggested to be a major upstream molecule in the activation of inflammatory factors, including IL-6 and TNF-α, by playing an important role in macrophage polarization and activation. In addition, several investigations have suggested a strong link between Gal-3BP levels and metabolic disorders, consistent with systemic pro-inflammation, by influencing inflammatory signalling pathways, including JNK-STAT and IKKβ/NF-κB [20–23]. There is solid evidence that insulin resistance is related to inflammation with both the fluctuation of cytokines and the relevant signalling pathways. For example, IL-6 is reported to induce insulin resistance by impairing the synthesis of glycogen and enhancing TLR-4 gene expression through the activation of STAT3 [24]. Menopause-triggered insulin resistance is also considered to partly rely on the decreased protective effect of oestrogen on the inflammatory response. Interestingly, Eva Olga Melin et al found that high Gal-3BP levels were associated with HbA1c only in women. These findings suggest that Gal-3BP may be associated with sex hormone fluctuation and have an impact on insulin resistance by systemic immune regulation. Further studies on the relationship between sex hormones and Gal-3BP expression are needed.
Some limitations of this work must be taken into consideration. First, the design of the observational study cannot implicate the cause-and-effect relationship. Second, the diagnostic criteria for insulin resistance were mainly based on HOMA-IR indices and not hyperinsulinaemic-euglycaemic clamp analyses. Finally, due to the small number of subjects, the trials may have weaknesses that could result in bias.
Despite these limitations and to our knowledge, this study found a significant and close relationship between Gal-3BP and insulin resistance in menopausal women, but the underlying mechanisms need further investigation, and the relationship between Gal-3BP and sex hormones is necessary and important to be clarified in future investigations.
Ethics approval and consent to participate
The study protocol was approved by the Ethical Committee of Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine. Written informed consent was obtained from all participants in the study. The study was conducted according to the Declaration of Helsinki.
Consent for publication
Not applicable.
Competing interests
The authors declare that there are no competing interests.
Funding
This study was supported by the Major Science and Technology Programme and Key Projects of the Science and Technology Department of Zhejiang Province, China (grant 2014C03044-1).
Authors’ contributions
Cai has full access to the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analyses.
1) conceived and designed the experiments: Cai.
2) performed the experiments: Chen, Zhuo and Cai.
3) analysed and interpreted the data: Chen and Das.
4) contributed reagents, materials, analytical tools or data: Chen and Cai.
5) wrote the paper: Chen and Das.
Acknowledgements
The authors thank Professor Yueming Chen for valuable discussion and the staff of the central laboratory for assistance with the experiments.
Availability of data and materials
We are currently planning a related study. Therefore, the data and material are not shared in their current state. However, the datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Table.1 Demographic characteristics and physical and metabolic measurements overall and across quartiles of HOMA-IR indices
|
Overall (n=62) |
Quartiles of HOMA-IR indices |
p-value |
|||
4 (n=16) |
3 (n=16) |
2 (n=14) |
1 (n=16) |
|||
Age (years) |
58.2±5.5 |
56.0±5.6 |
61.3±4.7 |
59.4±4.8 |
56.3±5.5 |
0.012 |
BMI (kg/m2) |
25.1±1.3 |
25.8±1.1 |
24.6±1.7 |
25.2±0.9 |
24.6±0.9 |
0.016 |
SBP (mmHg) |
124.3±11.6 |
131.0±5.1 |
123.0±15.6 |
121.0±11.0 |
121.8±10.5 |
NS |
DBP (mmHg) |
73.0 (69.0-79.0) |
79.0±5.3 |
72.5±9.8 |
67.1±7.0 |
75.5±6.0 |
0.000 |
TC (mmol/L) |
5.47 (5.09-5.87) |
5.60±0.82 |
5.53±0.71 |
5.41±0.37 |
5.70±1.11 |
NS |
TG (mmol/L) |
1.97 (1.62-2.38) |
2.39±0.60 |
1.92±0.74 |
2.02±0.54 |
1.87±0.50 |
NS |
HDL-C (mmol/L) |
1.20 (1.13-1.35) |
1.29±0.27 |
1.21±0.20 |
1.26±0.20 |
1.27±0.20 |
NS |
LDL-C (mmol/L) |
3.33 (3.12-3.70) |
3.41±0.59 |
3.43±0.54 |
3.27±0.47 |
3.43±0.86 |
NS |
FPG (mmol/L) |
4.95 (4.85-5.38) |
5.12±0.46 |
5.46±0.65 |
4.98±0.30 |
4.89±0.31 |
0.005 |
FINS (mU/L) |
6.88 (4.78-11.34) |
14.32±2.25 |
8.46±1.51 |
6.14±0.62 |
4.19±0.50 |
0.000 |
HOMA-IR index |
1.73 (1.05-2.42) |
3.26±0.58 |
2.02±0.23 |
1.36±0.15 |
0.91±0.12 |
0.000 |
ALT (U/L) |
26.0 (22.0-38.0) |
45.1±29.5 |
27.5±12.4 |
25.9±5.4 |
28.1±12.4 |
0.010 |
Gal-3BP (ng/ml) |
1734.23 (1243.34-2323.45) |
2916.72±1089.59 |
1656.64±523.27 |
1598.23±476.67 |
1455.58±763.76 |
0.000 |
Abbreviations: SBP systolic blood pressure; DBP diastolic blood pressure; TC total cholesterol; TG triglycerides; HDL-C high-density lipoprotein cholesterol; LDL-C low-density lipoprotein cholesterol; FPG fasting plasma glucose; FINS fasting insulin; HOMA-IR homeostasis model assessment-insulin resistance; ALT alanine transaminase; NS No significant difference.
Table 2. Correlation between Gal-3BP and anthropometric/metabolic parameters in all subjects
variables |
Age |
BMI |
SBP |
DBP |
TC |
TG |
HDL-C |
LDL-C |
FPG |
FINS |
HOMA-IR |
ALT |
r |
-0.045 |
0.226 |
0.012 |
-0.095 |
-0.216 |
-0.022 |
0.003 |
-0.144 |
-0.073 |
0.517 |
0.513 |
-0.083 |
p-value |
0.729 |
0.077 |
0.925 |
0.46 |
0.092 |
0.868 |
0.981 |
0.262 |
0.572 |
0.000** |
0.000** |
0.522 |
** p-value<0.01.
Table.3 The influence of factors on the HOMA-IR index by multiple regression analysis
Factor |
Unstandardized Coefficients |
Standardized coefficients |
t |
p-value |
|
B |
S.E. |
Beta |
|||
Age |
0.015 |
0.005 |
0.250 |
2.869 |
0.008** |
BMI |
0.058 |
0.021 |
0.224 |
2.712 |
0.009** |
SBP |
0.002 |
0.003 |
0.083 |
0.794 |
0.431 |
DBP |
0.086 |
0.035 |
0.247 |
2.484 |
0.016* |
TC |
-0.860 |
2.346 |
-0.157 |
-0.366 |
0.716 |
TG |
0.831 |
0.262 |
0.327 |
3.169 |
0.003** |
HDL-C |
0.038 |
0.183 |
0.025 |
0.209 |
0.835 |
LDL-C |
0.075 |
0.208 |
0.138 |
0.358 |
0.722 |
FPG |
0.118 |
0.030 |
0.340 |
3.965 |
0.000** |
Gal-3BP |
0.668 |
0.125 |
0.482 |
5.363 |
0.000** |
ALT |
0.065 |
0.035 |
0.189 |
1.883 |
0.065 |
** p-value<0.01; * p-value<0.05.
Table 4. Quality of cut-off scores for the prediction of impaired insulin resistance
HOMA-IR index cut-off |
AUC (95%CI) |
Gal-3BP cut-off |
Sensitivity, % |
Specificity, % |
1.5 |
0.6752 (0.5420-0.8085) |
2234.3150 |
42.1 |
83.3 |
2.0 |
0.809 (0.685-0.933) |
2234.3150 |
42.1 |
83.3 |
2.5 |
0.927 (0.862-0.992) |
2234.3150 |
100 |
84 |
AUC area under the curve.