Association of Obesity-Mediated Insulin Resistance and Hypothalamic Volumes: Possible Sex Differences

Ha, Jenny; Cohen, Jessica I.; Tirsi, Aziz; Convit, Antonio

doi:https://doi.org/10.1155/2013/531736

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Volume 35 | Article ID 531736 | https://doi.org/10.1155/2013/531736

Association of Obesity-Mediated Insulin Resistance and Hypothalamic Volumes: Possible Sex Differences

Jenny Ha,¹Jessica I. Cohen,¹Aziz Tirsi,¹and Antonio Convit^1,2,3

Academic Editor: Viswanath Devanarayan

Received07 Jun 2013

Revised25 Jul 2013

Accepted07 Aug 2013

Published11 Sept 2013

Abstract

The hypothalamus is important in hunger and metabolism. Although a lot is known about the basic role of the human hypothalamus, less is known about how the in vivo volume is affected in obesity, particularly among adolescents. Based on pediatric body mass index percentiles, 95 participants were assigned to lean or obese groups. All subjects had medical evaluations, including fasting blood tests, to assess insulin sensitivity and circulating CRP and neurotrophins (NGF and BDNF) and an MRI of the brain. Hypothalamic volumes were measured by a segmentation method combining manual and automated steps. Overall, obese participants had descriptively smaller hypothalamic volumes, although this difference did not reach statistical significance; however, among obese participants, females had significantly smaller hypothalamic volumes than their male counterparts. There was a significant interaction between insulin resistance and sex on hypothalamus volume; obese females with significant insulin resistance have smaller hypothalamic volumes than obese males. Obese adolescents had higher circulating CRP and neurotrophin levels. Furthermore, among obese females, BDNF concentrations were inversely associated with hypothalamus volumes (). Given this negative association between BDNF and hypothalamus volumes among obese insulin-resistant females, elevated neurotrophin levels may suggest an attempt at protective compensation.

1. Introduction

The prevalence of obesity is increasing at an alarming rate worldwide. In the United States, this trend is especially alarming in children and adolescents. According to the Centers for Disease Control, in 2008, 18.1% of adolescents (12–19 years old) were considered obese, which is 3-fold higher than that in the 1980s [1]. Adolescent obesity is a strong predictor of adulthood obesity as excessive weight gain occurring in adolescence is unlikely to decrease over time [2]. Obesity can lead to many comorbid conditions such as hypertension, atherosclerosis, and type 2 diabetes [3], and weight gain during adolescence may increase the risks for these morbidities in adulthood [4]. Furthermore, obese adolescents with type 2 diabetes, as well as those with metabolic syndrome, show reductions in cognitive performance and white matter microstructural integrity [5]. Reductions in hippocampal volumes and increases in global brain atrophy are also observed in these adolescents with clinical and preclinical metabolic diseases [5–7]. Unlike the hippocampus, little is known about the impact of obesity on the in vivo volume of the hypothalamus. The hypothalamus is a small but complex and multifunctional area of the brain that is involved in autonomic, endocrine, and behavioral functions. It is comprised of several nuclei that serve specific functions such as food intake and metabolic control [8–10]. The working model for hypothalamic regulation of food intake and energy balance is the set-point theory [11], and obesity may be associated with an elevated set point [12], which differs between individuals and may fluctuate throughout one’s life [13]. Given the importance of the hypothalamus in the control of nutrient intake and metabolism [14] and since the majority of hypothalamus and obesity studies have been conducted utilizing animal models [15, 16], the need for human studies is pressing.

There is evidence that more female adolescents are diagnosed with type 2 diabetes than male adolescents [17]. It is known that females with type 2 diabetes, despite better glucose control than males with diabetes, have greater hippocampal volume reductions than those observed in males [18]. In addition, females with type 2 diabetes are at greater risk for cardiovascular disease, increased risk of mortality from coronary heart disease, and end-stage renal disease than age- and weight-matched males [19–21]. Furthermore, females are also more likely than their male counterparts to have dyslipidemia [22–24]. Given the strong connection between obesity and hypothalamic inflammation [25–27], as well as the higher rates of inflammation among females [28, 29], ascertaining whether obesity impacts hypothalamic volumes and whether females are disproportionately affected is of considerable interest and could be a significant contribution to the field.

Obesity is considered a chronic inflammatory condition [30]. Neurotrophins, such as brain-derived neurotrophic factor (BDNF) and nerve growth factor (NGF), protect neurons from inflammatory events [31]. The hypothalamus and hippocampus contain the highest levels of BDNF expression [32]. BDNF gene expression, which is mediated by NGF, increases in response to inflammation and is involved in many conditions, such as inflammatory bowel disease [33, 34] and age-associated myocardial injury [35]. Previous studies show conflicting data regarding BDNF expression in obese adolescent populations, with some studies reporting BDNF reductions in obese subjects [36] and others reporting elevations [37]. Although a previous report demonstrated that late pubescent boys have greater BDNF levels than late pubescent girls, this was based on a small sample size. In contrast, adult women have been reported to have higher BDNF levels than men [38]. A previous study reported elevated serum BDNF levels in female adults with type 2 diabetes compared to healthy female controls [39]. In addition, elevations in NGF have been associated with obesity and metabolic syndrome in women [40]. Furthermore, our group has reported that although adult women with obesity-associated impaired insulin function have lower BDNF levels overall, those with poorer memory performance had higher BDNF levels, perhaps as a compensatory mechanism [41]. A recent study [42] illustrated differences in the inflammatory profile seen in obese adolescents compared to what is seen in obese adults, although acute-phase reactants, such as C-reactive protein (CRP) and fibrinogen, were elevated in obese adolescents compared to lean controls, consistent with adult literature [43–46]; no such differences were seen in pro- or anti-inflammatory cytokines. For these reasons, we were interested in ascertaining whether there may be differences in neurotrophins, even though differences in cytokines were not observed.

We hypothesized that although increased BMI and waist circumference (and their associated increases in inflammatory cytokines) were associated with smaller adult hypothalamic volumes, given the lack of clear elevations in inflammatory cytokines in obese adolescents, obese adolescents’ hypothalamic volumes will be indistinguishable from those of healthy weight adolescents. Further, we also proposed that compensatory mechanisms, such as possible increases in peripheral neurotrophin concentrations, which have been shown to reflect central BDNF levels [47], may protect the hypothalamus from injury and contribute to the hypothesized absence of hypothalamic volume reductions among obese adolescents. However, given the sex-specific increases in inflammation and the greater vulnerability of the female brain to metabolic-related damage, we further hypothesized that the associations between excess weight and hypothalamic volumes may differ by sex among adolescents. To test these hypotheses, we performed MRI-based hypothalamic and third ventricle volume measurements by utilizing a modification of other published methods [48–52] and ascertained whether group or sex differences were influenced by differences in inflammatory markers and neurotrophins.

2. Methods

2.1. Participants

Thirty-two lean and 63 obese adolescents, well-matched on age (calculated by subtracting the participants’ self-reported birth date from the date of their first visit to our laboratory), sex, ethnicity (self-reported according to NIH standards; please see http://grants.nih.gov/grants/funding/women_min/race_ethnicity_qa.htm#1027), and socioeconomic status [53], were included in the study (Table 1). The subjects were consecutive cases evaluated as part of an NIH-sponsored study approved by the New York University School of Medicine Institutional Review Board. All of the participants (and if they were under 18 years of age, one of their parents) signed informed consent and received compensation for their time and inconvenience. Potential participants were screened to rule out exclusionary preexisting medical (hypertension, dyslipidemia, polycystic ovary disease, or insulin resistance were permitted) and psychiatric conditions. Additionally, potential subjects were excluded if they had a history of significant head trauma, hydrocephalus, mental retardation, or neurological disorders. Because we excluded individuals with a history of neurological and psychiatric diseases prior to entering the study, we did not encounter any brain abnormalities that were exclusionary. Potential participants were also excluded if they were on medication other than cholesterol, diabetes, hypertension, and/or asthma. Namely, psychoactive medications and corticosteroids were excluded. Among the type 2 diabetic participants, medications included netformin, Novolog, and Glucophage. Participants’ height (Seca 220, Germany) and weight (Seca 700, Germany) were measured during a physical examination. Those who were 18 years and older with a body mass index (BMI) ≤ 24.9 kg/m² were considered lean, and participants with a BMI ≥ 30 kg/m² were included in the obese group. Participants who were younger than 18 and had a BMI-for-age < 85th percentile and ≥95th percentile were considered lean and obese, respectively. None of the participants were on medications (i.e., anti-inflammatory drugs, beta agonists) that could confound our results. Participants with a CRP > 10 mg/L were excluded from CRP analyses, because we could not exclude that they were due to a minor infection (such as acne) and not reflective of chronic low-grade proinflammatory state.

2.2. Classification of Participants into Those with and without Insulin Resistance

By definition, adolescents with a diagnosis of type 2 diabetes mellitus have marked insulin resistance. Also, because adolescents with type 2 diabetes can in most cases still mount a strong insulin response, they have a high degree of fasting insulinemia. Adolescents without type 2 diabetes were considered insulin resistant if they had a homeostasis model assessment of insulin resistance (HOMA-IR) score, an estimate of insulin resistance determined from fasting insulin and glucose values, ≥3.99 [54–56]. For all fasting blood draws, participants were instructed not to consume any food or beverage, with the exception of water, after 10:00 pm. the night prior to blood collection. This resulted in 10–12 hours of fasting. Furthermore, given that in our experience obese adolescents with type 2 diabetes and those with marked insulin resistance and metabolic syndrome have very similar brain structural abnormalities [5, 7], we placed obese adolescents with type 2 diabetes and those with marked insulin resistance into one group for some analyses.

2.3. Blood Collection

Following 10–12 hours of fasting, blood was collected from all participants at 09:00 am in a standardized fashion. Standard blood tests, such as cellular blood count with differential, comprehensive metabolic profile including glucose and insulin levels, lipid profile, hemoglobin A1C, CRP, and fibrinogen levels, were performed at the NYU Medical Center Clinical Laboratories. The high-sensitivity (cardio) CRP level was measured using an enzymatic immunoassay slide (VITROS CRP, Ortho Clinical Diagnostics). Using blood samples collected in fluorinated tubes, the fasting blood glucose level was measured using a glucose oxidase method (VITROS 950 AT, Johnson & Johnson), and insulin was assayed using chemiluminescence (Advia Centaur, Bayer corporation). Total cholesterol, high density lipoprotein (HDL-C), low-density lipoprotein (LDL-C), and triglycerides levels were analyzed using chemistry slides (VITROS DT, Johnson & Johnson). The glycated-hemoglobin level was measured using an automated method (HPLC, Tosoh Corporation) certified by the National Glycohemoglobin Standardization Program. In addition to the blood samples used for the clinical labs, samples were collected in EDTA tubes, placed immediately on ice, and spun at 4°C at 2,300 RPM for 10 minutes, and the plasma was stored at −80°C for neurotrophin assays (see below), which were performed at the NYU Clinical Translational Science Institute core laboratory.

2.4. Circulating Neurotrophin Measurements

Plasma samples previously stored at −80°C were thawed on ice. Enzyme-linked immunosorbent assays (ELISA) using multiplex plates (Millipore, Billerica, MA, USA) were performed on a subset of the population (18 lean and 31 obese). The plates arrived from the manufacturer precoated with antibodies to the proteins of interest. Plasma samples were loaded onto the plates per the manufacturer’s instructions (50 μL of plasma was used) and read on a Luminex plate reader (Austin, TX, USA) which detects fluorescent intensity. Protein concentration was determined by comparing the unknown sample concentrations to those of a standard curve. The coefficients of variance were between 7.2 and 9.4%.

2.5. Magnetic Resonance Imaging

2.5.1. Brain MRI Acquisition

All participants were scanned on the same 1.5T Siemens Avanto MRI system (Siemens Healthcare, Malvern, PA, USA) utilizing identical sequence parameters. For the volume measurements, a T1-weighted magnetization-prepared rapid acquisition gradient echo (MPRAGE) sequence was acquired in the coronal pathological angle (TR 1300 ms; TE 4.38 ms; T1 800 ms; FOV ; 196 slices; slice thickness 1.2 mm; NEX 1; flip angle 15°). To rule out white matter diseases and to ensure that subjects met the inclusion and exclusion criteria, fast fluid-attenuated inversion recovery (FLAIR; TR 9000 ms; TE 97 ms; FOV 210 × 201; 1 average and 2 concatenations; flip angle 145°) images were used. Subjects with evidence of infarcts, hemorrhages, intracranial masses, hydrocephalus, or significant white matter lesions were excluded from the study.

The MPRAGE images were intensity normalized and then used to define operator-based regions of interest (ROIs) for the volumetric analyses. All ROIs were drawn blind to participants’ identity, endocrine data, and group membership. Reformatted sagittal images were created, and the dural and cerebellar tentorium margins were outlined across multiple slices to estimate intracranial vault (ICV) size, which was then used to correct for head-size variations across participants. For more details, refer to Gold et al. [57].

2.5.2. Volumetric Hypothalamus Measurements and Determination of Boundaries

By building on several established methods [48–52], we utilized an in-house manual drawing program (MIDAS.1.11) to create the ROI for the hypothalamus on coronal slices. We defined the anterior boundary of the hypothalamus as the first coronal slice, where the complete anterior commissure (AC) was visualized crossing the interhemispheric space (Figures 1(a), 1(b), and 1(d)). As the majority of hypothalamic nuclei are located anterior to the mammillary bodies, we defined the posterior boundary of the hypothalamus as the coronal slice that included the posteriormost aspect of the mammillary bodies (Figures 1(c) and 1(d)) [58].

(a)

(b)

(c)

(d)

Figure 1

Anatomical landmarks for the determination of the hypothalamus and third ventricle (3V) regions of interest (ROIs). (a) Anteriormost coronal view showing the anterior commissure (AC) and optic chiasm (OC). (b) Hypothalamus (red), third ventricle (3V, blue), and anterior commissure and posterior commissure (AC-PC) plane (green) ROIs on the anteriormost coronal slice of the hypothalamus region. (c) Posteriormost coronal view showing the 3V, mammillary bodies (MB), and optic tracts (OT). (d) Hypothalamus, 3V, and AC-PC plane ROIs on the posteriormost coronal slice of the hypothalamus region.

The superior boundary of the hypothalamus was defined as the horizontal plane that connects the anterior and the posterior commissures (AC-PC plane). The PC was found approximately 24 mm (about 20 coronal slices) posterior to the coronal plane, where the AC bisected the interhemispheric plane (the anterior boundary of the hypothalamus). By using a volume of interest function in MIDAS.1.11, the AC and PC were connected and the superior boundary plane was visible on all of the coronal planes spanning the AC-PC distance (Figures 1(b) and 1(d)). The inferior boundary on anterior slices was the center of the optic chiasm (excluding the infundibular stalk) (Figures 1(a) and 1(b)). On posterior sections, the inferior boundary of the hypothalamus region was defined as the ventralmost aspect of the mammillary bodies (Figures 1(c) and 1(d)).

We utilized the optic tracts as a readily identifiable lateral margin level for the hypothalamus (Figures 1(b), 1(c), and 1(d)). The white matter that demarcates the histological lateral boundaries of the hypothalamus is not readily visible on the MRI. By using the optic tracts, which are positioned lateral to this white matter, and coupling the lateral boundary defined by the optic tracts with an automated gray-white segmentation within these boundaries (see below), we were able to increase our interrater reliability. In most cases the hypothalamus, so defined, spanned 96–120 mm in the anterior-posterior dimension (8–10 coronal sections).

To utilize the volume of the third ventricle as a related (albeit separate) measure of hypothalamic structural integrity, we utilized the same anterior, posterior, superior, and inferior boundaries of the hypothalamus and drew lateral boundaries on the third ventricle that included some gray matter as well as all the easily identified CSF (Figures 1(b) and 1(d)). A precise lateral boundary was not needed given that a segmentation step, which will be described in detail immediately below, would remove the extraneous gray matter.

The brains were segmented into gray matter and white matter and CSF using Statistical Parametric Mapping 2 (SPM2) software (University College London, London, UK) and Matlab 6.0 (MathWorks, Natick, MA, USA). Our thresholds for gray matter and CSF were set to intensities between 0.50–1.00 and 0.75–1.10, respectively. The hypothalamic ROI was intersected with the gray matter segment. Those portions that were not included represented the white matter tracts adjacent to the hypothalamus on each slice (Figure 2). Any gray matter that appeared lateral to these unbiased and automatically determined white matter tracts was manually removed. The third ventricle ROI was intersected with the CSF segment without subsequent manual removal of excess CSF. These procedures generated the hypothalamus and third ventricle volumes.

(a)

(b)

(c)

To estimate the interrater reliability of our method, two investigators independently performed the measurement on 10 randomly selected cases. Interrater reliability was assessed for the middle slice of the hypothalamic region (if the hypothalamus was present on an odd number of slice sections, the middle slice was chosen; if the hypothalamus was present on an even number of slices, the anterior slice of the two possible slices was chosen) as well as for the entire hypothalamic volume. The interclass correlation coefficients (ICC) for the middle slice and total hypothalamus volumes were 0.86 and 0.91, respectively.

2.6. Statistical Analysis

Data were analyzed using SPSS for Windows version 19.0 (SPSS, Inc., Chicago, IL, USA). The Kolmogorov-Smirnov and Shapiro-Wilk tests were used to test for normality. Independent -tests, with a 95% confidence interval, were used to investigate group differences in HOMA, total cholesterol, HDL, LDL, fibrinogen, systolic blood pressure, intracranial vault volumes, and residualized hypothalamus and third ventricle volumes. The Mann-Whitney test, with a nonparametric 95% confidence interval, was used to investigate group differences in nonnormally distributed variables. A Pearson correlation coefficient was used to assess the relationship between circulating BDNF measurements and hypothalamus volumes (accounting for ICV, residualized) in the obese group. In the linear and hierarchical regressions investigating the interaction between the effects of sex, BMI, and HOMA-IR on hypothalamus volume, sex, ethnicity, and blood pressure were used as potential confounds. To adjust for head-size variability, hypothalamus and third ventricle volumes were adjusted (residualized) to ICV size using analysis of variance.

3. Results

3.1. Demographic Data

There were no significant group differences in age, sex, and socioeconomic status. As expected, obese adolescents had significantly higher BMI, waist circumference, and waist-to-height ratios compared to the lean group (). Additionally, obese adolescents had higher fasting glucose (), hemoglobin A1C, fasting insulin, CRP, fibrinogen, and HOMA-IR values (all ). The obese group also had lower HDL, higher LDL and triglycerides concentrations, and higher blood pressure than the lean group (Table 1). None of the adolescents in the lean control group met criteria for significant insulin resistance (type 2 diabetes or HOMA-IR ≥ 3.99), whereas within the obese group, 40 (23 females and 17 males) adolescents (63%) fulfilled this criterion. Obese insulin-resistant adolescents, in addition to the expected differences in HOMA-IR, fasting insulin, fasting glucose, and hemoglobin A1C values from the noninsulin-resistant obese adolescents, also differed on BMI, waist circumference, triglycerides, and systolic blood pressure. LDL, HDL, CRP, and fibrinogen did not differ between these two obese subgroups.

3.2. Neurotrophin Concentrations

The subgroup with available neurotrophin data did not differ from the group that did not have these data in age, sex, or obesity status Circulating concentrations of BDNF were significantly higher in the obese group (mean ± SD, min–max) (, 45.9–535.0) compared to the lean group (, 20.4–210.0) (), whereas NGF was not statistically significant (lean , 0.42–7.24; obese , 1.81–11.50) (). No sex differences were found when comparing all males and females or when comparing the lean and obese groups separately.

3.3. Hypothalamus Volumes

The hypothalamic volumes obtained were in keeping with those expected from histological studies [59]. See Table 2 for the group mean volumes. Please note that Table 2 describes the absolute volume measurements. There was a significant correlation between hypothalamus and ICV volumes (, for all participants; , for obese participants), therefore, volumetric analyses were performed utilizing ICV-adjusted (residualized) hypothalamus volumes. Overall, obese participants had descriptively smaller hypothalamic volumes, although they did not differ statistically (, , and df = 89). Similarly, there were no overall weight group differences in the middle hypothalamus slice volume. The volume of the third ventricle and ICV also did not differ between groups (Table 2). Given the reported sex-associated differences in inflammation as well as the higher rate of medical and brain complications from metabolic disease among women, despite the lack of overall hypothalamus obesity group difference, we explored whether there were sex differences in hypothalamus volume separately for each of the two BMI groups. We found that relative to obese males, obese females had smaller hypothalamic volumes, () (Table 3). No such sex differences existed among lean individuals. Furthermore, lean and obese males and lean and obese females also did not differ in hypothalamic volumes.

There was a significant inverse relationship between BDNF levels and residualized hypothalamus volumes in obese girls (, ), whereas none existed in obese boys (, ) (Figure 3). We found no association between hypothalamic or third ventricle volumes with either of our two markers of low-grade inflammation, CRP, and fibrinogen, or NGF (data not shown).

3.4. Sex and Significant Insulin Resistance Contribute to Hypothalamic Volume

A factorial ANOVA, performed on the whole dataset, revealed a significant interaction between the effects of sex and insulin resistance on residualized hypothalamic volume, (, ) (Figure 4). Simple effect analysis showed that there were significant hypothalamus volume differences in the group with insulin resistance ( females and 16 males; ), but there was no sex difference in the lean controls ( females and 18 males; ). There was no interaction between the effects of sex and BMI on hypothalamic volume () in the insulin-resistant group when a factorial ANOVA was performed. These interactions and results persisted when BMI and HOMA were used as continuous variables.

4. Discussion

To our knowledge, this is the first report of volumetric differences in the hypothalamus between obese male and female youth. Overall, obese participants had descriptively smaller hypothalamic volumes, although they did not differ statistically. However, when divided further by sex, obese females had significantly smaller ICV-adjusted hypothalamic volume than obese males. Moreover, this sex effect is driven by metabolic dysregulation (those with type 2 diabetes or insulin resistance short of diabetes having the smallest volumes) and is associated with circulating BDNF concentrations.

Measuring the volume of the hypothalamus in vivo presents significant challenges. Unlike the hippocampus, the hypothalamus is not a discrete structure but rather a group of nuclei. Building on the work of other groups [48–51], we utilized a method that allowed us to very reliably measure the volume of the hypothalamus. By using a clearly operationalized anatomical approach in conjunction with unbiased automated segmentation, we were able to clearly separate out the hypothalamus from the surrounding white matter. Utilizing clearly defined anatomical boundaries, assisted by unbiased segmentation to highlight the hard-to-see white matter tracks, resulted in high interrater reliability with an ICC of 0.86 and 0.91 for the middle slice volume and total hypothalamus volume, respectively. Previous work from our lab shows that obesity and insulin resistance have detrimental effects on several regions of the brain, specifically the orbitofrontal cortex, hippocampus, frontal lobe, and amygdala [6, 18, 60–62]. Furthermore, females with type 2 diabetes have significantly smaller hippocampal volumes than age-matched males with type 2 diabetes, despite the females being in overall better glucose control [18]. In addition to adverse effects on the brain, adult women, ranging from 20–70 years of age, are more susceptible to metabolic syndrome and cardiovascular disease than men [63, 64]. Furthermore, females tend to have a higher levels of inflammatory markers than males [28, 29], and the hypothalamus is particularly sensitive to damage caused by inflammation [25].

Less is known about the differential sex impact of obesity-mediated insulin resistance on brain in the youth. Nevertheless, the evidence in adults outlined above is in keeping with our current findings that obese adolescent females with marked insulin resistance have smaller hypothalamus volumes than their obese male counterparts. The volumetric differences are likely the result of an interaction between sex and insulin resistance, as shown by the very significant interaction shown in Figure 4. Association between inflammation and hypothalamus damage has been reported in animals [65–67], and there is some preliminarily data in humans [65]. However, we and others have failed to find evidence of clear association between obesity/insulin resistance and cytokine elevations [42], so whether low-grade inflammation affects hypothalamic volumes in the youth remains to be determined. With that being said, although obesity has been clearly associated with elevations in acute-phase reactants during adolescence, we failed to find any association between high-sensitivity CRP and hypothalamic volumes.

Another possible mechanism that may contribute to the observed volumetric differences is changes in vessel integrity. It is well established that obesity has a deleterious effect on endothelial function [68, 69]. It is possible that altered endothelial function in vessels that supply certain vulnerable brain regions could play a role in the decreased hypothalamic volumes described here.

Conditions that result in increased inflammation, such as irritable bowel disease, are often associated with increases in neurotrophic factors [33, 34]. This increase in neurotrophins, particularly BDNF, may in part occur to protect neurons from inflammatory damage [31]. Our obese adolescents, similar to previous reports in obesity [70, 71], showed increased levels of circulating CRP and fibrinogen, as well as elevations in BDNF (Figure 3). Neurotrophins are also associated with eating behavior [72–74]. Mice deficient in BDNF become hyperphagic [73], and low circulating levels of BDNF can lead to anorexia nervosa or trigger episodes of binge eating [74]. Obese adolescents had higher concentrations of circulating BDNF. It is possible that these increases represent a compensatory mechanism, to both protect the brain from injury and to be an attempt to decrease food consumption. Although previous studies have inconsistently associated BDNF levels with adolescent obesity, given that the adolescents in the present study were in average of 17.5 years of age, these increased BDNF levels may reflect adult-like compensatory mechanisms in response to excess weight [75]. Furthermore, our obese females displayed a strong inverse relationship between circulating BDNF levels and hypothalamic volumes. It is important to note that obese females, after adjusting for their smaller ICV sizes, did have smaller hypothalamic volumes than obese males. This suggests that there may be other mechanisms at work that the BDNF cannot compensate for. For example, females are known to have more brain abnormalities in diabetes despite being in better glucose control than their male counterparts [18], so it is possible that sex hormones, which are known to have direct effects on obesity and adipose tissue [76], may also partly mediate these sex differences.

Although this study has numerous strengths, such as our high interrater reliability, the study is not without its limitations. We utilized a cross-sectional design which does not allow us to determine if obesity is the cause or result of smaller hypothalamic volume in obese females compared to obese males. Given that this is an in vivo human study, we measured circulating neurotrophins instead of measuring the localized brain neurotrophins. Thyroxin, thyroid stimulating hormone [77–79], and gonadotropin levels [80, 81], which may be dysregulated by obesity and insulin resistance, were not assessed in this study and should be evaluated in follow-up studies.

Future efforts should try to identify which hypothalamic nuclei may be compromised in obese youth with insulin resistance and whether with meaningful weight loss, which has been shown to partially reverse hypothalamic dysfunction [26], and reversal of insulin resistance, these volume changes are reversed and whether the tissue recovery is associated with reductions in the hypothesized compensatory BDNF elevations.

Abbreviations

AC:	Anterior commissure
BDNF:	Brain-derived neurotrophic factor
BMI:	Body mass index
CRP:	C-reactive protein
CSF:	Cerebral spinal fluid;
ELISA:	Enzyme-linked immunosorbent assay
FLAIR:	Fast fluid-attenuated inversion recovery
HOMA-IR:	Homeostasis model assessment of insulin resistance
ICC:	Interclass correlation coefficients
ICV:	Intracranial vault
IR:	Insulin resistance;
LDL:	Low-density lipoprotein
LHA:	Lateral hypothalamic area
MIDAS:	Multimodal image data analysis system
MPRAGE:	Magnetization-prepared rapid acquisition gradient echo
MRI:	Magnetic resonance imaging
NGF:	Nerve growth factor
PC:	Posterior commissure
ROI:	Region of interest
SPM:	Statistical Parametric mapping
VMH:	Ventromedial hypothalamus.

Authors’ Contribution

Jenny Ha and Jessica I. Cohen have contributed equally to this paper and should be considered co-first authors.

Conflict of Interests

None of the authors have any financial or conflicting interests to disclose.

Acknowledgments

This study was supported by a Grant from the National Institutes of Health DK 083537 (Antonio Convit) and T32-DA 007254-16 (Jessica I. Cohen) and supported in part by Grant 1UL1RR029893 from the National Center for Research Resources.

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