Proinflammatory and lipid biomarkers mediate metabolically healthy obesity: A proteomics study

Abstract

Objective

The metabolically healthy obesity (MHO) phenotype is an important obesity subtype in which obesity is not accompanied by any metabolic comorbidity. However, the underlying molecular mechanisms remain elusive. In this study, a shotgun proteomics approach to identify circulating biomolecules and pathways associated with MHO was used.

Methods

The subjects were 20 African‐American women: 10 MHO cases and 10 metabolically abnormal individuals with obesity (MAO) controls. Serum proteins were detected and quantified using label‐free proteomics. Differential expression of proteins between the two groups was analyzed, and the list of differentially expressed proteins was analyzed to determine enriched biological pathways.

Results

Twenty proteins were differentially expressed between MHO and controls. These proteins included: hemoglobin subunits (HBA1, P = 6.00 × 10⁻¹⁸), haptoglobin‐related protein (HPR, P = 1.2 × 10⁻¹⁵), apolipoproteins (APOB‐100, P = 1.50 × 10⁻⁴⁰; APOA4, P = 1.1 × 10⁻¹⁴), retinol‐binding protein 4 (RBP4, P = 7.1 × 10⁻⁰⁸), and CRP (P = 2.0 × 10⁻⁰⁴). MHO was associated with lower levels of proinflammatory and higher levels of anti‐inflammatory biomarkers when compared with MAO. Pathway analysis showed enrichment of lipids and inflammatory pathways, including LXR/RXR and FXR/RXR activation, and acute phase response signaling.

Conclusions

These findings suggested that protection from dysregulated inflammatory and lipid processes were primary molecular hallmarks of MHO. The candidate biomarkers (AHSG, RBP4, and APOA4) identified in this study are potential prognostic markers for MHO.

Introduction

Obesity has reached epidemic proportion globally 1, 2. Annually, 300,000 excess deaths are linked to obesity and its complications, making obesity the second leading cause of premature death 3. Obesity is a major contributor to the global burden of disabilities and chronic diseases including high blood pressure (BP), type 2 diabetes (T2D), and heart diseases 1, 2. While obesity triggers a range of complications, the most common complication is T2D, which is usually preceded by a state of insulin resistance (IR) before T2D is actually diagnosed 4. Paradoxically, it has been documented that not all individuals develop IR or T2D or other cardiometabolic co‐morbidities as they gain weight, a phenomenon referred to as metabolically healthy obesity (MHO). This paradox has led to the claim that “not all obese humans are created equal” 5. MHO subjects were first described about 30 years ago 6 with recent extensive description by Karelis et al. and many other investigators 6, 7, 8, 9, 10. Using the presence of metabolic abnormalities as a classifying variable, individuals with obesity can be grouped into: MHO (also known as the insulin sensitive individuals with obesity) and the metabolically abnormal subjects with obesity (MAO), or the insulin resistant individuals with obesity. Reported prevalence of MHO varies between 10% and 40% of all subjects with obesity and with prevalence varying by many factors including age, ethnic background, and level of physical activity 11, 12. Interestingly, interventions such as weight loss in MHO had no apparent benefit or may even be detrimental as shown by a study conducted by Shin et al. and others 13, 14.

There is evidence that the MHO phenotype is not stable and that many such individuals eventually develop metabolic abnormalities 15, 16, 17. While many MHO may convert to MAO over time, there is a substantial proportion of MHO who remain protected from obesity‐related abnormalities 18. The MHO phenotype seems to span the entire life‐span and has been observed in individuals in their ninth decade of life, as demonstrated in the National Health and Nutrition Examination Survey (NHANES) study in which MHO was 22.1% among individuals with obesity 80 years and older 19. These observations suggest that the phenotype provides an opportunity to investigate the factors that distinguish MHO from MAO and thereby gain insight into biomarkers and molecular mechanisms that are involved in the development of cardiometabolic abnormalities. Most studies of the MHO phenotype have been epidemiological studies 7, 8, 18, 20, 21, 22, and only a few have focused on the molecular basis of MHO.

In the present study, we use a shotgun proteomics approach to evaluate differential protein expression between MHO and MAO individuals. By identifying differentially expressed proteins (DEPs) in serum samples of MHO compared with MAO, we aim to gain biological insights into the underlying biological mechanisms that mediate the MHO phenotype.

Methods

Subject selection and study design

The individuals included in this study were selected from a well‐phenotyped cohort of African Americans (AA) recruited in the Washington, DC, area to study the genetic epidemiology of complex diseases in populations of African descent, the Howard University Family Study (HUFS). Briefly, the main objective of the HUFS was to enroll and examine a randomly obtained sample of African‐American families along with a set of unrelated individuals for study of the genetic and environmental bases of common complex traits including hypertension, obesity, diabetes, and associated phenotypes. In order to maximize the utility of this cohort for the study of multiple common traits, families and individuals were not selected based on any phenotype. All participants were recruited after an overnight fast of at least 8 hours prior to the blood draw and all collected samples were stored in a −80°C freezer pending measurement of biochemical parameters 22. This study was approved by Howard University's institutional review board (IRB) and informed consent was obtained from each participant.

Case definition of MHO

Since this study is exploratory, we used very stringent definitions to select individuals included as MHO or MAO. A combination of three definitions of MHO was applied as follows:

• Definition 1: No hypertension (BP ≤ 130/85, no BP medication), no diabetes (glucose ≤ 126 mg/dL), HDL‐C ≥ 40 mg/dL for men and ≥ 50 mg/dL for women, all conditions have to be met. This is the basic MHO definition.

• Definition 2: No hypertension (BP ≤ 130/85, no BP medication), no diabetes (glucose ≤ 100 mg/dL), HOMA ≤ 5.1, TG/HDL ≤ 1.65 for men and ≤ 1.32 for women, all conditions have to be met. This is the modified Wildman et al. definition 19.

• Definition 3: All definition 2 criteria + hsCRP ≤ 0.3 mg/dL, all conditions have to be met. This third definition takes into account inflammatory status. The C‐reactive protein (CRP) cutoff used was based on Karelis et al. recommendations 9.

The subjects included had to meet all three definitions, that is, these individuals (cases) would be identified as MHO by all three definitions (Figure 1, Supporting Information Table S1).

Figure 1.

Flowchart for MHO case selection. 1, definition 1: No hypertension (BP ≤ 130/85, no BP medication), no diabetes (glucose ≤ 126 mg/dL), HDL‐C ≥ 40 mg/dL for men and ≥50 mg/dL for women, all conditions have to be met. 2, definition 2: No hypertension (BP ≤ 130/85, no BP medication), no diabetes (glucose ≤ 100 mg/dL), HOMA ≤ 5.1, TG/HDL ≤ 1.65 for men and TG/HDL ≤ 1.32 for women, all conditions have to be met. 3, definition 3: definition 2 + hsCRP ≤ 0.3 mg/dL. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com.]

Definition of controls (MAO)

MAOs were selected if they were individuals with obesity who had four or all five of the following abnormalities: hypertension, no diabetes but glucose level higher than 100 mg/dL, HOMA >5.1, TG/HDL >1.65 for men and >1.32 for women, and hsCRP >0.3 mg/dL).

About 10 MHO cases and 10 MAO controls meeting these criteria were studied.

Serum proteomics

Serum shotgun proteomics were done at the National Cancer Institute, Proteomics Core Lab. Serum samples were depleted of 14 highly abundant proteins using Agilent's Multiple Affinity Removal System (MARS) spin cartridges which are 0.45 mL immunoaffinity cartridges packed with antibody‐modified resin (Agilent Technologies, Santa Clara, CA) (list of the 14 proteins depleted, Supporting Information Table S2). The enriched pool of low abundant proteins were then collected and combined from several flow‐through fractions. Quality control measures were used to assess depletion efficiency by removing an aliquot of both the low and high abundant pools and subsequently resolving the proteins on a 4%‐12% SDS‐PAGE gel. Proteins were visualized by staining with Coomassie blue.

A BCA assay was used to determine the protein concentration of the low abundant protein pools. The samples were desalted and concentrated by buffer exchange using 5,000 Da molecular weight cutoff (MWCO) spin concentrators followed by protein digestion using sequencing grade modified trypsin at a 1:20 trypsin‐to‐protein ratio. Resultant peptides were then subjected to solid phase extraction followed by fractionation using strong cation exchange (SCX) chromatography.

Each SCX peptide fraction was analyzed by microcapillary reversed‐phase liquid chromatography tandem mass spectrometry (µRPLC‐MS/MS) using an Agilent 1100 capillary LC system (Agilent Technologies, Santa Clara, CA) coupled online to a linear ion trap mass spectrometer (LTQ, Thermo Electron, Waltham, MA). Separations were performed using 75 μm i.d. × 360 μm o.d. × 10 cm long fused silica capillary ESI emitter columns (Polymicro Technologies, Phoenix, AZ) slurry‐packed in‐house with 3 μm, 300 Å pore size C‐18 silica (Vydac, Hysperia, CA). The mass spectrometer was operated in data‐dependent MS/MS mode with each full MS scan being followed by seven MS/MS scans where the seven most intense peptide molecular ions in the MS scan were sequentially and dynamically selected for collision‐induced dissociation (CID). Dynamic exclusion was employed to minimize redundant acquisition of tandem mass spectra.

Mass spectra were searched against a Uniprot human proteomic database using SEQUEST. A tryptic enzyme restriction with a maximum of two internal missed cleavage sites was used and methionine residues were considered modified in the database search. For a fully tryptic peptide to be considered legitimately identified, it had to achieve stringent charge state and proteolytic cleavage‐dependent cross correlation (Xcorr) scores of 1.9 for [M + H]¹⁺, 2.2 for [M + 2H]²⁺, 3.1 for [M + 3H]³⁺, and 4.5 for [M + 4H]⁴⁺, and a minimum delta correlation (ΔCn) of 0.08. SEQUEST results were further filtered and analyzed using software developed in‐house. The output is peptide count (PC) data in which columns represent peptide counts (peptide abundance) in each experimental sample and rows represent distinct proteins detected in the samples.

Data quality control and data analysis

A total of 16,553 proteins were identified, at least once, among the 20 subjects. The proteomics data were analyzed using DanteR/InfernoRDN R‐based software packages designed to analyze quantitative proteomics data 23. Only proteins detected in both groups (n = 7,836 proteins) were retained for analysis. The proteomics data were reported as PC which follows a Poisson distribution. To determine DEPs among the two groups, analysis of variance (ANOVA) was carried out using Poisson regression. P‐values were corrected for multiple testing using Benjamin and Hochberg (FDR) and the threshold for significance was P < 0.05. The list of DEPs was submitted to Ingenuity pathway analysis (IPA) to determine biological functions and pathways that were enriched (IPA^®, QIAGEN Redwood City, www.qiagen.com/ingenuity). The IPA biological functions analysis calculates the probability of a set of DEPs being associated with known biological functions/canonical pathways by chance alone. The significance of the association between the DEPs and the pathways was measured in two ways: (a) A ratio of the number of molecules from the DEP data set that map to the pathway divided by the total number of molecules that map to the canonical pathways, (b) P‐values obtained from Fisher's exact tests used to assess the probability that observed associations between the DEPs and the canonical pathway were due to chance alone; P‐values <0.05 were considered significant.

Anthropometric and clinical parameters were compared between the two groups by Student's t‐test using SPSS package. Data are presented as mean± standard deviation or median and interquartile range when appropriate.

Results

Characteristics of study groups

The anthropometric and clinical characteristics of the study subjects are summarized in Table 1. The cases (MHO) and the controls (MAO) individuals were not statistically different from each other in key parameters including age, BMI, PFM, and hip circumference. As expected, the six parameters (BP, glucose, HOMA‐IR, HDL‐C, TG, and hsCRP) used in the selection of the two groups are statistically different between the two groups. Notably, MHO had healthier lipid profiles with considerably lower TG and higher HDL‐C levels compared with MAO. Inflammation, measured by adiponectin and hsCRP, was minimal in MHO compared with MAO. Notably, adiponectin, an adipokine decreased in obesity, is paradoxically higher in this group of MHO, about 1.8 times higher than in the MAO group (8,074.0 ± 3,977.4 μg/mL vs. 4,486.8 ± 2,535.9 μg/mL).

Table 1.

Characteristics of study subjects (MAO vs. MHO)

Variable	MAO	MHO	P a
Age (years)	43.3 ± 7.8	41.3 ± 10.1	0.6
BMI (kg/m2)	44.7 ± 13.0	36.5 ± 5.7	0.08
Waist (cm)	120.8 ± 21.1	102.5 ± 16.0	0.04
Hip (cm)	134.3 ± 20.4	125.1 ± 15.0	0.3
WHR	0.90 ± 0.05	0.82 ± 0.06	0.004
PFM	49.1 ± 5.4	47.1 ± 5.8	0.4
SBPS (mmHg)	145.8 ± 25.1	118.2 ± 6.3	0.007
DBPS (mmHg)	86.4 ± 13.6	73.8 ± 4.8	0.01
Glucose (mg/dL)	103.0 ± 16.2	83.8 ± 4.5	0.004
Insulin (μU/mL)	67.1 ± 86.2	8.9 ± 3.9	0.04
HOMA‐IR	17.3 ± 23.6	1.8 ± 0.9	0.05
TG (mg/dL)	233.5 ± 186.6	83.8 ± 34.9	0.03
LDL‐C (mg/dL)	103.4 ± 35.3	130.5 ± 51.3	0.2
HDL‐C (mg/dL)	34.1 ± 8.6	62.2 ± 8.7	<0.001
Adiponectin (μg/mL)	4,486.8 ± 2,535.9	8,074.0 ± 3,977.4	0.03
hsCRP (mg/dL)	2.2 ± 1.5	0.2 ± 0.08	0.02

Values in this table represent mean ± standard deviation.

^aStudent's t‐test compared means between the two groups. P‐value <0.05 in bold.

Identification of DEPs among MHO and MAO

At total of 56 proteins were differentially expressed (33 upregulated and 23 downregulated) at an unadjusted P < 0.05 as shown on the volcano plot (Supporting Information Figure S1 and Supporting Information Table S3). After adjusting for multiple testing by the Benjamini and Hochberg method and using a P‐value threshold of <0.05, 20 proteins were differentially expressed between MHO and MAO including 8 downregulated and 12 upregulated in MHO compared with MAO (Table 2, Supporting Information Figure S2). Among the most upregulated in MHO were APOB‐100 (P = 1.5 × 10⁻⁴⁰, FC = 1.2) and alpha‐2‐HS‐glycoprotein (ASHG, P = 3.00 × 10⁻²⁹, FC = 1.7). Hemoglobin subunit alpha (HBA, P = 6.0 × 10⁻¹⁸, FC= 0.44) and haptoglobin‐related protein (HPR, P = 1.2 × 10⁻¹⁵, FC = 0.6) were downregulated in MHO compared with MAO. CRP was also confirmed to be downregulated in MHO by the proteomic data (P = 2.0 × 10⁻⁰⁴). Supporting Information Figure S3 is a principal components plot of the DEPs that shows separation of MHO and MAO subjects by PC1, PC2, and PC3, indicating the discriminant ability of these 20 proteins.

Table 2.

Differentially expressed proteins among MHO and MAO African‐American women determined by label‐free serum proteomics

Accession #	Protein name	Gene symbol	Log effect size (log2FC)	P MHO unadjusted	P MHO BH	Average PC in MHO	Average PC in MAO
8 under‐expressed proteins in MHO compared with MAO
P69905	Hemoglobin subunit alpha	HBA1	−1.17	3.1 × 10−21	6.00 × 10−18	8.5	27.5
P00739	Haptoglobin‐related protein	HPR	−0.78	7.6 × 10−19	1.2 × 10−15	19.2	42.1
P68871	Hemoglobin subunit beta	HBB	−0.80	4.6 × 10−15	4.5 × 10−12	13.8	30.8
P00751	Complement factor B	CFB	−0.21	1.4 × 10−10	1.1 × 10−07	172.7	212.6
Q14624	Inter‐alpha‐trypsin inhibitor heavy chain H4	ITIH4	−0.16	3.0 × 10−09	1.70 × 10−06	242	285.1
P02741	C‐reactive protein	CRP	−2.13	4.00 × 10−07	2.0 × 10−04	1.2	10.1
P27169	Serum paraoxonase1	PON1	−1.16	1.5 × 10−06	7.0 × 10−04	2.44	7.8
P0C0L4	Complement C4‐A	C4A	−0.081	2.8 × 10−06	1.0 × 10−03	638.4	692.5
12 over‐expressed proteins in MHO compared with MAO
P04114	Apolipoprotein B‐100	APOB	0.28	1.9 × 10−44	1.5 × 10−40	563.1	423.7
P02765	Alpha‐2‐HS‐glycoprotein	AHSG	0.75	7.7 × 10−33	3.00 × 10−29	79.1	37.4
P01008	Antithrombin‐III	SERPINC1	0.41	3.50 × 10−26	9.2 × 10−23	163.8	108.2
P06727	Apolipoprotein A‐IV	APOA4	0.40	8.5 × 10−18	1.10 × 10−14	113.8	76.1
P05155	Plasma protease C1 inhibitor	SERPING1	0.71	4.6 × 10−15	4.5 × 10−12	37	18.2
P02753	Retinol‐binding protein 4	RBP4	0.46	8.1 × 10−11	7.1 × 10−08	51.5	32.5
P19823	Inter‐alpha‐trypsin inhibitor heavy chain H2	ITIH2	0.19	2.3 × 10−10	1.6 × 10−07	249.5	206.6
P06396	Gelsolin	GSN	0.25	3.4 × 10−10	2.25 × 10−07	135.1	104.3
P04196	Histidine‐rich glycoprotein	HRG	0.30	8.9 × 10−10	5.3 × 10−07	99.4	73.8
P19827	Inter‐alpha‐trypsin inhibitor heavy chain H1	ITIH1	0.15	7.5 × 10−07	0.0004	228.9	196.6
P02774	Vitamin D‐binding protein	GC	0.17	1.7 × 10−06	0.0007	165.8	139.3
P10643	Complement component C7	C7	0.36	1.8 × 10−05	0.007	34.9	24.4

Cutoff P‐value < 0.05.

Enriched biological pathways in the most differentially expressed proteins in MHO compared with MAO

We used IPA to identify enriched biological pathways in the 20 DEPs. The most significant enriched canonical pathways include LXR/RXR activation (P = 1.4 × 10⁻¹⁵), FXR/RXR activation (P = 1.9 × 10⁻¹⁵), acute phase response signaling (2.9 × 10⁻¹⁴), and complement system (P = 4.6 × 10⁻⁰⁸) (Figure 2, Table 3). Interestingly, a number of the enriched pathways are interconnected through DEPs that are common to more than one canonical pathway. For example, acute phase response signaling has three and four DEPs in common with complement system (C4A/C4B, CFB, SERPING1) and LXR/RXR activation (AHSG, C4A/C4B, ITIH4, RBP4), respectively (Figure 3, Table 3). Figure 4 depicts DEPs mapped to the most significant enriched canonical pathways.

Figure 2.

Canonical pathways significantly enriched in the 20 DEPs. Bars represent total number of molecules in a pathway; upper Y‐axis represents the ratio between the number of molecules in our data set that are associated with a pathway and the total number of molecules in that pathway; lower Y‐axis represents –log of the P‐value associated with each pathway. X‐axis lists the top pathways associated with the DEPs. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com.]

Table 3.

DEPs associated with the most significantly enriched canonical pathways

Name of canonical pathways	Associated DEPs	Overlap ratioa	P‐valueb
LXR/RXR activation	AHSG, APOA4, APOB, C4A/C4B GC, HPR, ITIH4, PON1, RBP4	9/121 (7.4%)	1.4 × 10−15
FXR/RXR activation	AHSG, APOA4, APOB, C4A/C4B, GC, HPR ITIH4, PON1, RBP4	9/125 (7.2%)	1.9 × 10−15
Acute phase response signaling	AHSG, C4A/C4B, CFB, CRP, HRG, ITIH2, ITIH4, RBP4, SERPING1	9/168 (5.4%)	2.9 × 10−14
Complement system	C4A/C4B, CFB, SERPING1	4/36 (11.1%)	4.6 × 10−08
Atherosclerosis signaling	APOA4, APOB, PON1, RBP4	4/121 (3.3%)	6.3 × 10−06

^aNumerator of ratio represents the number of DEPs in our data set that map to the canonical pathway; the denominator represents the total number of molecules/proteins that map to the pathway.

^b P‐value obtained by Fisher's exact test.

Figure 3.

Overlap between the top canonical pathways enriched in the 20 DEPs. Black lines: interconnectivity between canonical pathways; red boxes: significantly enriched canonical pathways in the study. Numbers on black lines represent the number of proteins common to two interconnected pathways. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com.]

Figure 4.

Two of the most significantly enriched canonical pathways in MHO. (A) Acute phase reactant signaling in MHO overlapped with DEPs. (B) LXR/RXR activation in MHO overlapped with DEPs. Red: proteins upregulated in our data set; the intensity of the color indicates the degree of upregulation. Green: proteins downregulated in our data set; the intensity of the color indicates the degree of downregulation. White: proteins not specific to our data set but incorporated as part of the network. [Color figure can be viewed in the online issue, which is available at wileyonlinelibrary.com.]

Discussion

Despite considerable interest in this subset of MHO subjects, the underlying molecular mechanisms remain largely unknown. Understanding the pathophysiology of MHO is important not only for this subset of individuals but also for obesity as a whole. Here, we describe the results of the first study to use high‐throughput omics technology, namely shotgun label‐free quantitative proteomics, to profile the proteome and obtain a comprehensive snapshot of differences in protein expression between MHO and MAO African‐American women.

The DEPs between MHO and MAO underscored important inflammation‐related proteins including AHSG, CRP, histidine‐rich glycoprotein (HRG), retinol‐binding protein 4 (RBP4), complement factor‐4A (C4A), and inter‐alpha‐trypsin inhibitor heavy chain H4 (ITIH4). These molecules belong to the family of acute phase reactant proteins (APP) and are primarily produced by the liver in response to injury and infection 24, but some (e.g., RBP4) are also produced by adipocytes 25. It is well documented that inflammation is a key component of obesity and has been associated with the progression and development of obesity‐related complications 26. In this study, the APPs differentially expressed can be categorized into two groups, the negative APPs (AHSG, HRG, and RBP4) all of which were over‐expressed in MHO, and the positive APPs (HRP, CRP, C4A, and ITIH4) which in contrast to the negative APPs were downregulated in MHO. These changes suggest a favorable inflammatory profile associated with MHO.

Some of these molecules have also been involved in adverse metabolic events such as impairment of insulin signaling, fatty liver diseases, and suppression of adiponectin production 25, 27, 28, 29, 30, 31. For example, high levels of AHSG, a glycoprotein produced by hepatocytes, have been linked to metabolic syndrome in certain populations 28, 30. However, the association seems to vary with gender as one report showed an association between high AHSG and metabolic syndrome in Japanese men but not in women 32. While our study showed that AHSG is upregulated in MHO, we did not see any of the other reported changes associated with elevated AHSG. For example, the MHO in this study had high adiponectin levels compared with MAO (8,074.0 ± 3,977.4 μg/mL vs. 4,486.8 ± 2,535.9 μg/mL) and remained insulin sensitive based on their HOMA‐IR values (1.8 vs. 17.3). These results suggest at least two hypotheses—(a) AHSG is regulating its effectors differently in this MHO cohort or (b) a threshold in AHSG concentration needs to be reached to see its effects on metabolic markers such adiponectin and insulin. In the latter scenario, AHSG may be a potential biomarker on its own or in combination with other proteins (e.g., RBP4, APOA4, APOB) to identify MHO that will convert into MAO.

RBP4, an adipokine with differential regulation in animals and humans and involved in the transport of vitamin A to peripheral tissues, has been associated with dysfunction of insulin signaling especially in animal models. However, in humans the positive association between RBP4 levels and IR has not been consistent 25, 29, 33. RBP4 could also be a promising marker to follow the changes in MHO especially now that the MHO phenotype has been shown to be a transient state for many affected individuals 12.

The complement system pathway, part of the humoral immune system and involved in inflammatory processes, was over‐represented among the DEPs associated with MHO. As expected, all DEPs (C4A/C4B, CFB, SERPING1) associated with the complement system were also associated with the acute phase reactant pathway showing a commonality between the over‐represented pathways. All but SERPING1 were downregulated, thus agreeing with the lower inflammation profile seen in MHO. In fact, SERPING1 is an inhibitory regulator of the complement cascade and may play a role in inflammation suppression. SERPING1 has been shown to be downregulated in patients with T2D compared with healthy controls 34.

Nine of the DEPs (AHSG, APOA4, APOB, C4A/C4B, GC, HPR, ITIH4, PON1, and RBP4) were associated with lipid metabolism. Four of these DEPs are involved in both inflammatory and lipid processes (AHSG, C4A/C4B, ITIH4, and RBP4), underscoring the pleiotropic function of some of the DEPs. Previous studies have found an association between AHSG and RBP4 and serum lipids (mainly triglycerides [TG] and HDL‐C) 27, 35. APOB‐100, APOA4, and PON1 are all members of the HDL/LDL family. APOA4 is secreted by enterocytes along with TG and chylomicrons. For example, APOA4 has anti‐oxidant and anti‐inflammatory properties and is proposed to be protective against cardiovascular diseases. It also plays a role in glucose homeostasis and satiety (reduces food intake) 36. Interestingly in T2D and obesity, increased levels of APOA4 have been found to be mainly related to hypertriglyceridemia 37. In this study, APOA4 is upregulated without hypertriglyceridemia; while the mechanisms involved need further investigation, the absence of hypertriglyceridemia seems to be protective in MHO.

A major strength of the study is the stringent and conservative approaches used to define MHO individuals (cases). Three distinct definitions of MHO were used and only individuals who were classified as MHO by all three definitions were selected and studied. Though this approach decreases the pool of MHO, it is more effective in reducing misclassification. In contrast to a recently published metabolomics study in MHO in which the definition of MAO used may have resulted in heterogeneous metabolic phenotypes 38, this study included only MAO with all four or five metabolic abnormalities. Secondly, the differential proteomic method combined with bioinformatics analysis (IPA) demonstrated changes in serum protein profiles in MHO individuals that were not previously reported.

While very promising, the insights provided by this study into the molecular basis of MHO should be interpreted within the following context—(a) by design, this study is a discovery investigation and as such the findings need to be confirmed in larger and diversified populations; (b) the cross‐sectional design provides only a snapshot of the proteome and causality should not be inferred; and (c) important confounding factors that may affect the serum proteome including level of physical activity and diet were not analyzed in this study. While earlier studies did not find any difference in dietary profile and physical activity between MHO and MAO 11, 13, 18, 26, a recent study with larger sample sizes and the use of healthy eating index (HEI) showed that MHO have a better dietary compliance to the US guidelines than MAO including intake of more whole grains, fruits, and beans. However, the authors acknowledged that the effect seen may be due to reverse causality 39. Although diet and exercise are likely to affect biological functions in MHO, studies available to date have not specifically assessed inflammation and other biological functions in a systematic manner. Future omics studies, including whole genome microarray, miRNA profiling, and whole exome sequencing, investigating the determinants of the MHO phenotype will benefit from having data on potential lifestyle confounding variables such as physical activity and diets.

Conclusion

Our study is the first to use proteomics to investigate the mechanisms that are involved in the MHO phenotype. Our findings confirm previous reports that inflammation is a key hallmark of metabolic health in individuals with obesity but also identified a network of APPs, more than what was previously reported, to be involved in the inflammatory processes associated with MHO. Some of these proteins, mainly RBP4, AHSG, APOA4, PON1, and APOB‐100, could be good candidates to follow up in longitudinal studies to determine their ability to predict which MHO individuals convert to MAO. We also found that differential regulation of lipid metabolism is also important to the MHO phenotype.

Supporting information

Supporting Information