Invest Clin 64(3): 338 - 354, 2023 https://doi.org/10.54817/IC.v64n3a7
Corresponding author: Oralia Nájera Medina. Departamento de Atención a la Salud, División de Ciencias Básicas
y de la Salud, Universidad Autónoma Metropolitana Unidad Xochimilco (UAM-Xochimilco), Ciudad de México, Mé-
xico. Phone: (+52) (55) (5483 7000, ext. 2675. Email: onajera@correo.xoc.uam.mx
Modified High-Intensity Interval Training
and its effects on immunometabolic
regulation in sedentary young adults with
overweight and obesity.
Carmen Paulina Rodríguez-López
1
, María Cristina González-Torres
2
and Oralia Nájera-Medina
1
1
Departamento de Atención a la Salud, CBS, Universidad Autónoma Metropolitano-
Xochimilco (UAM-Xochimilco), Ciudad de México , México.
2
Departamento de Ciencias de la Salud, CBS, UAM-Iztapalapa, Ciudad de México,
México.
Keywords: obesity; physical activity; lymphocytes; metabolic syndrome; visceral fat.
Abstract. Sedentary lifestyles can contribute to obesity and other diseas-
es; while chronic low-grade inflammation associated with obesity can lead to
metabolic alterations. As physical activity is an alternative to decrease excess
weight and its related comorbidities, High-Intensity Interval Training (HIIT) has
recently emerged as effective in regulating whole-body metabolism and inflam-
matory processes in people with excess weight. The objective was to compare
the effects of a modified HIIT program on peripheral blood leukocytes (PBL),
metabolic profile, insulin resistance (IR), and body composition (BC) in sed-
entary adults with excess weight. PBL, biochemical variables, IR, and BC were
analyzed in 37 participants, 23 sedentary young adults (17 with overweight
and six with obesity), before and after eight weeks of a modified HIIT program
and compared with those of 14 healthy-weight participants. The results showed
that after HIIT, total lymphocytes, TCD3+, and TCD8+ lymphocytes decreased;
granulocytes and naïve TCD3+ cells increased in patients. Regarding partial
correlations, we found that changes (Δ) in TCD8+ lymphocytes correlated posi-
tively with glucose and LDL-c, while naïve TCD3+ cells correlated with total
cholesterol and LDL-c. Δ in TCD4+CD45RA+ cells correlated negatively with Δ
in subcutaneous fat tissue and body fat mass. This study reports that sedentary
young adults who completed the modified HIIT program showed lymphocyte
levels similar to those in healthy-weight individuals and positive changes in the
study variables. Such changes suggest immunometabolic regulation through
the implementation of HIIT in participants with overweight and obesity.
High-Intensity Interval Training improves immunometabolism in sedentary obesity 339
Vol. 64(3): 338 - 354, 2023
Entrenamiento modificado de intervalos de alta intensidad
y sus efectos sobre la regulación inmunometabólica en adultos
jóvenes sedentarios con sobrepeso y obesidad.
Invest Clin 2023; 64 (3): 338 – 354
Palabras clave: obesidad; actividad física; leucocitos; síndrome metabólico; grasa
visceral.
Resumen. El sedentarismo puede contribuir a obesidad y otras enfermeda-
des; la
inflamación crónica de bajo grado asociada a la obesidad puede llevar a
alteraciones metabólicas. La actividad física es una alternativa para disminuir
el exceso de peso y sus comorbilidades asociadas, donde el Entrenamiento de
Intervalos de Alta Intensidad (HIIT, por sus siglas en inglés) ha emergido como
un regulador del metabolismo del cuerpo y del proceso inflamatorio en personas
con exceso de peso. El objetivo de esta investigación fue analizar los efectos del
programa de HIIT modificado sobre leucocitos en sangre periférica (LSP), perfil
metabólico, resistencia a la insulina y composición corporal (CC) en 37 partici-
pantes, 23 con exceso de peso (17 con sobrepeso y 6 con obesidad), después de
ocho semanas del entrenamiento y compararlos con 14 participantes con peso
saludable. Se encontró que los linfocitos totales, linfocitos TCD3+ y TCD8+
disminuyeron; los granulocitos y las células TCD3+ vírgenes aumentaron. En
cuanto a las correlaciones parciales, encontramos que los cambios (Δ) en los
linfocitos TCD8+ se correlacionaron positivamente con la glucosa y LDL-c,
mientras que las células TCD3+ vírgenes correlacionaron con colesterol total
y LDL-c. Δ en células TCD4+CD45RA+ correlacionaron negativamente con Δ
en tejido adiposo subcutáneo y masa grasa corporal. Estos resultados mostra-
ron que los adultos sedentarios que completaron el entrenamiento presentaron
niveles de linfocitos similares a los de los participantes con un peso saludable y
cambios positivos en las variables de estudio. Tales cambios sugieren una regu-
lación inmunometabólica en los participantes con sobrepeso y obesidad.
Received: 20-12-2022 Accepted: 27-04-2023
INTRODUCTION
About one-third of the world popula-
tion aged 15 years and older do not engage
in sufficient physical activity. Consequently,
health risks associated with a sedentary life-
style are on the rise. Sedentary lifestyles and
behaviors have several negative effects on
the human body including, ‘risks of meta-
bolic disorders such as diabetes mellitus, hy-
pertension, and dyslipidemia’
1
.
Obesity has been considered a chronic
low-grade inflammatory process character-
ized by an increase in the baseline number
of leukocytes and an imbalance between pro-
and anti-inflammatory cytokines in circula-
tion
2-4
. Such a condition is associated with
insulin resistance (IR)
5
, which is character-
ized by impaired insulin function in meta-
bolically essential tissues, affecting lipid ho-
meostasis and glucose and contributing to
metabolic disorders
6,7
.
340 Rodríguez-López et al.
Investigación Clínica 64(3): 2023
It has been proposed that weight gain
and its related comorbidities can be re-
versed through caloric restriction and in-
creased physical activity
8
. In addition, it has
been found that relative health benefits can
emerge even in those cases in which there is
no change in total sedentary time but inter-
mittent physical activities are included
1
. In
this respect, it has been observed that regu-
lar exercise is an effective measure against
chronic diseases as it improves the inflam-
matory profile
9
.
Recently, modern lifestyles have in-
creasingly promoted sedentary behavior
also among young adults. Against this back-
ground, High-Intensity Interval Training
(HIIT) has emerged as an alternative that
‘burns many calories in a short time, so
busy people can be more inclined to incor-
porate intermittent bursts of exercise into
their schedule’
10
. HIIT effectively regulates
whole-body metabolism
11,12
, enhances insu-
lin signaling, and improves anthropometric
measures and body composition (BC)
13-14
. In
addition, HIIT has been associated with im-
munomodulatory effects with potential anti-
inflammatory benefits
4
.
Although positive effects of HIIT have
been reported concerning obesity, little is
known about the relationship between dif-
ferent variables like body composition, met-
abolic profile, lymphocyte subpopulations,
and inflammatory response. Because the
problem of obesity has grown in recent years
and it is presented as a complex condition to
treat and because it implies lifestyle chang-
es, it is necessary to propose strategies to the
population that, in the short term, provide
them with some benefit, which is observable
as physical activity. Therefore, this study
aimed to investigate the effects of a modi-
fied HIIT program over eight weeks on the
variables mentioned above, peripheral blood
cells, metabolic profile, IR, anthropometric
measures, and BC in apparently healthy sed-
entary patients with overweight or obesity,
with or without metabolic syndrome (MS).
METHODS
Study design
A longitudinal clinical-trial study was
performed with sedentary young adults in
Mexico City, Mexico. The study was conduct-
ed following the Declaration of Helsinki,
and the protocol was approved by the Eth-
ics Committee of the Metropolitan Autono-
mous University of Xochimilco (Agreement
13/16,8.1). Participants provided written in-
formed consent before enrolling in the study.
The study population was selected ac-
cording to the following criteria:
Inclusion criteria: adults aged 18-40
years apparently healthy with overweight
(OW) or obesity (Ob) who did not engage in
regular and sufficient physical activities.
Exclusion criteria: individuals with any
infection, pregnant women, individuals with
diabetes mellitus type 1 or type 2 (DM2), or
autoimmune, hepatic, renal, endocrine, can-
cer, or heart disease, who were taking any
medication and/or participating in regular
exercise training, and who did not present a
medical certificate to engage in regular ex-
ercise.
The program included no dietary or ali-
mentary behavior modification to minimize
the influence of additional factors. All the
variables listed below were assessed before
and after two months of modified HIIT work-
outs. Measures were taken after at least 48 h
of the last exercise session to avoid data on
the acute effects of exercise. All the variables
listed below were evaluated at the beginning
and after two months (eight weeks) under a
modification of the HIIT training.
Se dentary behavior
Sedentary behavior was evaluated us-
ing an International physical activity ques-
tionnaire (IPAQ)-short form (7-day physical
activity). All participants were required to
complete the questionnaire in advance of the
study. An IPAQ activity level of <600 MET/
week was defined as sedentary behavior.
High-Intensity Interval Training improves immunometabolism in sedentary obesity 341
Vol. 64(3): 338 - 354, 2023
Clinical measurements
Anthropometric measurements were
performed following the standardized pro-
tocol of the International Society for the
Advancement of Kinanthropometry (ISAK)
15
(Although the person who made the mea-
surements for the study is not ISAK certi-
fied, it was standardized by someone who
is ISAK certified). A SECA 213 stadiometer
set at 0.1 cm of precision was used to mea-
sure height. Weight was measured using
InBody720 equipment (Biospace, Inc. Los
Angeles, CA, USA), and waist circumference
(WC) was measured employing SECA brand
201 (Chino, CA, USA) fiberglass tape. Nutri-
tional status was assessed through body mass
index (BMI) according to the World Health
Organization (WHO)
16
criteria for adults.
A dual-energy X-ray absorptiometry
(Hologic Discovery Wi. Hologic, Inc. Bed-
ford, MA, USA) was used to measure body
composition, obtaining data on skeletal
muscle mass (SMM, in kg), body fat mass
(BFM, in kg) and the percentage of body fat
(BF%). A multi-frequency impedance body
composition analyzer (InBody 720, equip-
ment) was utilized to obtain visceral adipose
tissue (VAT) in square meters, in which vis-
ceral obesity (increased VAT) was diagnosed
in persons with ≥100 cm
2
of fat and normal
VAT in persons with <100 cm
2
of fat).
Lipid and glucose measurements
For biochemical tests, 5 mL of a venous
blood sample was collected using an auto-
mated clinical chemistry equipment KON-
TROLab, model Ikem (KONTROLab Co., Ltd.
Roma, Italia), to obtain: triglycerides (TG);
high-density lipoprotein-cholesterol (HDL-
c), fasting glycemia (Glu), and total choles-
terol (TCho). Low-density lipoprotein-cho-
lesterol (LDL-c) was calculated based on the
Friedewald formula. Samples were obtained
after a 12-h fasting period. Blood pressure
measurements were performed according to
the guidelines of the Mexican Official Norm
(NOM-030-SSA2-1999). The presence of MS
was determined according to the Choles-
terol Education National Program (ATP III)
definition and modified according to the
Hispanic population
17
. These guidelines sug-
gest that MS is present when an association
of at least three of the following factors is
found: TG ≥150 mg/dL; HDL-c <40 mg/dL;
blood pressure ≥130/85 mmHg or a previ-
ous diagnosis; Glu ≥100 mg/dL, and a WC
in women of ≥80 cm and in men ≥90 cm.
Insulin resistance
The METabolic Scale for Insulin Resis-
tance (METS-IR) tool was employed to mea-
sure the IR parameter. This consists of an
indirect method for the detection of insulin
action that takes into account blood concen-
trations of TG, HDL-c, glucose, and BMI as
follows: (Ln((2*G0)+TG0)*IMC)/(Ln(HDL-
c)); G0: fasting glucose, and TG0: fasting
triglycerides
18
.
Measurement of lymphocyte
subpopulations
A 5 mL venous blood sample was collected
in tubes containing K
2
EDTA (BD Biosciences,
San Jose, CA, USA). Cells were stained with con-
jugated commercial antibodies (BD Bioscienc-
es, San Jose, CA, USA), and the combinations
employed were the following: FITC-anti-IgG1/
PE-anti-IgG2; FITC-anti-CD45/Pe-anti-CD14;
FITC-anti-CD3/PE-anti-CD16+CD56/PerCP-
anti-CD19; FITC-anti-CD4/PE-anti-CD62/
APC -anti-CD3; FITC-anti-CD8/PE-anti-CD28/
APC-anti-CD3, and FITC-anti-CD45RA/PE-
anti-CD45RO/PerCP-anti-CD4/APC-anti-CD3.
Peripheral blood samples were stained with
conjugated antibodies for 20 min in the dark,
then 3 mL of lysis buffer solution was added.
Samples were washed (PBS), fixed with 1%
p-formaldehyde, and analyzed within 24 h of
staining
4, 19
.Cell analysis was performed using
a FACSCanto II Cytometer with FACSDiva soft-
ware (BD Biosciences, San Jose, CA, USA). For
each sample, 10,000 cells were counted.
Intervention
HIIT group participants were super-
vised along three HIIT exercise sessions per
342 Rodríguez-López et al.
Investigación Clínica 64(3): 2023
week for eight weeks. Each training session
consisted of 25 min of effective exercise, and
each minute was divided into 30-s intervals
of activity, followed by a 30-s of active rest
(Active rests refers to the participants did
not stop moving altogether; they continued
jogging; it was rest from the exercises in-
volved in the session, such as squats or some
other exercise). Effective exercise time and
intervals increased according to the partici-
pants’ capacity. Eventually, the exercise ses-
sion consisted of 45 min of active exercise,
while each minute consisted of 50-s intervals
of activity, followed by 10-s of active rest. On
the recommendation of the Centers for Dis-
ease Control and Prevention, the American
College of Sports Medicine, and the Ameri-
can Heart Association
20
, sessions were orga-
nized into three parts.: warm-up (5-9 min),
aerobic part/resistance (HIIT) (25-45 min),
and cooling/flexibility (8-12 min).The ac-
tivity intensity was measured according to
the Perceived Exertion Rating Scale (RPE),
managed at moderate intensity (between 5
and 6)
21
. As HIIT works with high-intensity
intervals and since we worked with seden-
tary subjects with overweight and obesity,
a modification to this training system was
introduced in order to work at moderate in-
tensity. In addition, the Karvonen formula
(Functional Capacity Evaluation [FCE]=
{(FM-FR)*PI} + FR) was adapted, and the
percentage of intensity (PI) at which partici-
pants worked was obtained by taking into
account heart rate (FCE), resting frequency
(RF), and maximal frequency (MF) during
the training sessions)
22
. For the latter, the
FC was taken at each session before and af-
ter the training.
The participants’ adherence to the
study was calculated as the percentage of
complete sessions attended in relation to
the total number of training sessions pro-
posed in the present study.
Statistical analysis
The ShapiroWilk test was utilized to
determine whether the variables presented
had a Gaussian distribution. Logarithmic
transformation was performed to calculate
the normality in variables without Gauss-
ian distribution. The results are presented
as means ± standard deviations (SD) and
medians, employing an interquartile range
(IQR, 25-75). Paired Student t-tests were
employed to compare pre-and post-exer-
cise data. The One-way analysis of variance
(ANOVA) and Bonferroni post-hoc tests were
applied to determine differences between
>two groups. Data were adjusted for gender
and age. Bilateral partial correlation analy-
ses adjusted for gender, age, and BMI were
performed to estimate the correlation of the
Δ of the lymphocyte subpopulations with the
Δ of the anthropometric, BC, and biochemi-
cal variables. Then, step-wise forward linear
regression models utilizing the Δ of lym-
phocyte subpopulations as dependent vari-
ables to evaluate the association with Δ of
anthropometric, BC, and biochemical vari-
ables adjusted for gender, age, and BMI were
performed. A p<0.05 was considered signifi-
cant, using the IBM SPSS ver. 21 statistical
software program.
RESULTS
Forty overweight or obese persons were
accepted to participate in the training ses-
sions; however, several individuals withdrew
from the exercise (n=11). In addition, six in-
dividuals did not attend their second evalu-
ation. Thus, the study group consisted of 23
individuals. Remarking this way, the problem
that sedentary people have of adhering to a
routine.
Thirty-seven people participated, and
two groups were formed: 1) the control
group, consisting of 14 participants with
normal BMI, normal weight (NW), and VAT,
without MS, matched by gender and age with
the study group, who did not perform train-
ing, and 2) the study group, consisting of
23 persons with OW and Ob who underwent
the training. All participants included in the
study attended at least 80% of the classes
High-Intensity Interval Training improves immunometabolism in sedentary obesity 343
Vol. 64(3): 338 - 354, 2023
conducted. The average age of participants
was 26.4±6.5 years, and 73% were female.
Baseline characteristics
Thirty-seven percent of participants
(n=14) had normal BMI, 46% (n=17) peo-
ple with OW, and 16% (n=6) had Ob. A
prevalence of 26% (n=6) of MS was found
in the study group. It was also observed that
individuals with MS were mostly people with
visceral obesity.
Laboratory analysis, anthropometric
measurements, and BC
Regarding biochemical variables, it was
observed that persons with obesity had the
highest TG values compared to individuals
with NW and diastolic pressure in relation
to individuals with OW. It was also found
that HDL-c was lower in individuals with OW
than in those with NW. Concerning IR, it was
found that METS-IR increased as the BMI
did; therefore, individuals with NW present-
ed the lowest values and persons with Ob the
highest values; these differences were signif-
icant (Table 1).
Concerning anthropometric measure-
ments and BC, it was found that participants
with NW had the lowest values in WC, ST,
BFM, and VAT compared to individuals with
OW or Ob (Table 1).
Lymphocyte subpopulations
It was found that total lymphocytes
(TL) increased according to BMI. On the
other hand, granulocytes were lower in per-
sons with NW when compared with individu-
als with OW or Ob; all of these differences
were statistically significant. No significant
differences were observed when analyzing
the memory and naïve cells according to nu-
tritional status (Table 2).
Intervention
Overall, participants worked at 54 ±
10.6% of their maximal level according to the
formula of Karvonen. In addition, the inten-
sity percentage was increased as the training
weeks progressed, finding a significant dif-
ference between weeks 1 and 6 (46±13 vs.
61.9±10%, p<0.05).
Laboratory analysis, anthropometric
measurements, and BC
In individuals with OW or Ob, no sig-
nificant positive changes were found in bio-
chemical indicators after training by group
(Table 1). However, when each participant
was analyzed, it was found that TG decreased
in 39% of the participants by 25±14.7%, Glu
in 61% by 22±10%, TCho in 74% of individu-
als by 24±10%, LDL-c in 74% by 37±16%,
and HDL-c increased in 52% of persons by
20±10% (Fig. 1).Regarding anthropometric
measurements and BC after training, persons
with OW presented a statistically significant
decrease in WC (Table 1). Also, when each
participant was analyzed, it was found that
VAT decreased in 57% of the participants by
5.3±4.6cm
2
, ST in 57% by 1.9±2.2%, BFM
in 61% of individuals by 1.7±1.5kg, and
SMM increased in 30% by 1.3±1.6kg (Fig.
2). In addition, it was observed that one per-
son with Ob passed to OW and two with OW
passed to NW; furthermore, two persons with
increased VAT passed to normality.
Lymphocyte subpopulations
After training, TL and TCD8+ lympho-
cytes decreased in the study group. Also,
granulocytes and näive TCD3+ cells in-
creased.
When the subpopulations were analyzed
according to BMI, TL, TCD3+, and TCD8+
decreased in individuals with OW, approach-
ing the percentages of persons with NW. In ad-
dition, an increase of TCD3+CD45RA+ and
monocytes was found in persons with OW. All
of these differences were statistically signifi-
cant (Table 2). According to MS, we found that
TCD4+ lymphocytes decreased (55.6±13.2 vs.
29±13%; p<0.0001) after the training activ-
ity. In individuals without MS, the monocytes
increased (6.6±3.5 vs. 8.2±2.4%; p<0.0001),
while TCD8+ lymphocytes decreased (39±8.5
vs. 29.8±11.8%; p<0.05).
344 Rodríguez-López et al.
Investigación Clínica 64(3): 2023
Table 1
Biochemical indicators, anthropometric measurements, and body composition according to Body Mass Index
before and after two months of High-Intensity Integral Training.
Variable
(n=37)
Normal (n=14) Overweight (n=17) Obesity (n=6) p (ANOVA)
B A p# B A p# p
p (post
hoc)*&
TG (mg/dL) 80 ±26.5 119.8±52.6* 150.5±70.8 0.088 163.1±42.3* 187.3±58.9 0.188 0.002 0.002
c-HDL (mg/dL) 51.9 ±13.6 39.2* ±8.1 38.2 ±8.4 0.607 43.2 ±13.3 40.5 ±3.9 0.477 0.011 0.009
Glu (mg/dL)
81.1
(77.6-85.7)
79.4
(70.2-94.3)
83.8
(57.6-95.9)
0.597
81.2
(72.9-103.8)
78.7
(72.2-88.4)
0.226 0.754
c-LDL (mg/dL)
80.3
(64.9-93.6)
91.6
(60.9-130.3)
63.6
(46.4-88.7)
0.124
80.2
(46.7-144.1)
83.9
(48.1-99)
0.818 0.631
TCho (mg/dL)
146.9
(133.8-166.8)
161.7
(128.4-193.9)
140.2
(114-173.5)
0.608
165.3
(115.5-228.1)
156.9
(130.8-182.5)
0.757 0.628
SBP (mmHg) 105.5 ± 8.6 106.2 ±10.8 107 ±6.8 0.819 116.3 ±15.6 111.6 ±11.6 0.309 0.144
DBP (mmHg) 69.5 ±7 69.5 ±7.8 73.5 ±9.9 0.151 79 ±10.3& 76.6 ±5.1 0.675 0.049 0.059
METS-IR 31.8 ±4.2 42.4 ±4.9* 43 ±43 0.494 52 ±6.6*& 51.6 ±6.4 0.712 0.000 0.001
Weight (kg) 60.9 ±9.9 76.3 ±10* 75.9 ±10.4 0.328 87.1 ±17.5* 86.7 ±18.2 0.436 0.000 0.000
BMI (kg/m
2
) 22.5 ±1.7 27.3 ±1.3* 27.2 ±1.6 0.304 33.2 ±2.3*& 32.5 ±2.5 0.242 0.000 0.000
WC (cm) 81.2 ±7.4 90.9 ±6.4* 88.7 ±6.5# 0.001 102.7 ±10.5*& 99.7 ±11.2 0.187 0.000 0.000
SMM (kg) 23.8 (18.5-26.2) 26.3 (23.1-30.1) 26.6 (24.4-29.6) 0.949 23 (21.8-37) 23.6 (22-37.6) 0.131 0.150
ST (%) 27.7 ±6 35.5 ±5.9* 35 ±5.6 0.473 43.5 ±6.4*& 42.3 ±6.2 0.187 0.000 0.000
BFM (kg) 16.8 ±3.2 27 ±5.3* 27.2 ±6.8 0.822 37.1 ±3.8*& 36 ±4.7 0.258 0.000 0.000
VAT (cm
2
) 67.1 ±19 99.5 ±18* 98.5 ±18.8 0.500 139.9 ±28.6*& 138.5 ±33 0.722 0.000 0.000
Data are presented in media ± SD or median and interquartile range (IQR). p (post hoc): p adjusted with the Bonferroni test. # Statistically significant
difference between before and after. * Statistically significant difference vs normal. & Statistically significant difference vs overweighs (p<0.05). B: before;
A: after; TG: triglycerides; c-HDL: high-density lipoprotein cholesterol, Glu: glucose; c-LDL: Low-density cholesterol; TCho: total cholesterol; SBP: systolic
blood pressure; DBP: diastolic blood pressure; WC: waist circumference; SMM: skeletal muscle mass; ST: subcutaneous adipose tissue; BFM: body fat mass; VAT:
visceral adipose tissue.
High-Intensity Interval Training improves immunometabolism in sedentary obesity 345
Vol. 64(3): 338 - 354, 2023
Table 2
Leukocyte distribution before and after High-Intensity Integral Training according to Body Mass Index
Variable (n=34)
(%)
Normal
(n=11)
Overweight
(n=17)
Obesity
(n=6)
B A p# B A p# P*&
Total lymphocytes 29.3 ±10.9 40.3 ±9.6* 32.2 ±8.5# 0.048
53.5
±9*&
33.1±7.5# 0.029 0.000
Monocytes 7.8 ±2.4 7.1 ±3.1 8.4 ±2.2# 0.044 5.6 ±2.5 5.9 ±1.3 0.893 0.256
Granulocytes 62.6±11.1 52.4 ±8.5* 59.1±8.2 0.064 40.9±8.7* 60.7 ±6.6# 0.014 0.000
Lymphocytes B
7.5
(5-12.6)
7.4
(5.4-10.5)
9.2
(6.1-1.7)
0.148
11.6
(7.7-18.8)
15.2
(9.9-18.6)
0.293 0.202
Lymphocytes NK
19.5
(12.8-32.7)
14.3
(10.6-19.9)
16.6
(14.2-24)
0.171
13
(9.4-19.8)
20
(16.2-26.7)
0.199 0.430
TCD3+ 68.4 ±10.6 76.5 ±8.1 68.9±10.5# 0.043 71.2±10.9 62 ±9.3 0.244 0.112
TCD4+
56.9
(46-60.7)
52.2 ±7.7 43.5 ±16.5 0.139 51.4±13.7 38.4 ±19.5 0.568 .763
TCD8+ 29.8 ±14.9 38.7 ±7.8 29.6±12.1# 0.002 34 ±7.4 24.1±11.1 0.147 0.198
TCD3+CD45RA+ 54.2 ±13 48.5 ±11.6 53.4 ±8.7# 0.050 44.5±18.7 59 ±15.6 0.330 0.456
TCD3+CD45RO+ 32.1 ±9.4 31.6 ±8.7 31.4 ±5.8 0.792 39.7±14.9 26.1±9.5 0.230 0.358
TCD3+CD45RO+
CD45RA+
15.7 ±6 16.7 ±5.9 12.7 ±6.6 0.454 14.6 ±5.8 11.6 ±6.7 0.558 0.828
TCD4+CD45RA+ 36.4 ±14.7 20.3 ±7.2 35 ±17.3 0.438 33.9 ±5.1 52.5 ±15.2 0.160 0.521
TCD4+CD54RO+ 43.2 ±13.4 48.1 ±8.8 53.1 ±20.6 0.712 43 ±20.6 36 ±12.7 0.661 0.796
TCD4+
CD45RO+CD45RA+
17.6 ±5.8 16.7 ±6.1 11.5 ±3.8 0.250 24.4±15.4 11.8 ±5.7 0.444 0.395
Data are presented in means ± SD or median and interquartile interval (IIC).* Statistically significant difference vs normal. & Statistically significant diffe-
rence vs. overweight. # Statistically significant difference before vs. after (p<0.05). B: before; A: after; Lymph B: Lymphocytes B; Lymph NK: Lymphocytes
natural killer.
346 Rodríguez-López et al.
Investigación Clínica 64(3): 2023
Partial correlations were made of the ob-
served variations in leukocyte cells after the
intervention concerning the changes (Δ) in
the different variables, adjusting the analysis
by gender, age, and BMI. We found that Δ at
the peripheral level of the granulocytes and
TCD8+ lymphocytes correlated negatively
with Δ in WC; additionally, the Δ of TCD8+
lymphocytes correlated positively with glu-
cose and LDL-c. The Δ of the total näive
cells correlated positively with TCho and
LDL-c, and the Δ of the positive double cells
of TCD3+ (TCD3+CD45RA+CD45RO+)
positively correlated with the Δ in MERS-
IR. Last, the Δ of the näive cells of TCD4+
lymphocytes correlated negatively with the Δ
Fig. 1. Distribution and improvement of biochemical indicators after training.
Fig. 2. Distribution and improvement of anthropometric measurements and body composition after training.
High-Intensity Interval Training improves immunometabolism in sedentary obesity 347
Vol. 64(3): 338 - 354, 2023
percentage and kilograms of fat, all of these
differences statistically significant (Table 3).
No correlation was observed between exer-
cise intensity and change in lymphocyte sub-
populations.
Furthermore, we decided to perform a
linear regression adjusted for gender, age, and
BMI among the changes in lymphocyte sub-
populations statistically correlated with the
changes in the different variables. A positive
correlation was found between the changes of
TCD8+ lymphocytes and TCD3+CD45RA+
lymphocytes with changes in LDL-c, where a
decrease of 1 mg/dl of this cholesterol was
associated with a decrease of 3% (range, 0.8-
4.5%) of TCD8+ lymphocytes and an increase
of 6% (range, 2.8-9.6%) of TCD3+CD45RA+
lymphocytes. Also, TCD3+CD45RA+ lympho-
cytes correlated positively with TCho, where a
decrease of 1 mg/dL of this type of choles-
terol was associated with an increase of 7%
(range, 1-11%) of TCD3+CD45RA+ lympho-
cytes. Finally, TCD3+CD45RA+CD45RO+
lymphocytes correlated positively with METS-
IR, where a decrease of 1 unit of METS-IR was
associated with a decrease of 1% (range, 0.5-
2%) of TCD3+CD45RA+CD45RO+ lympho-
cytes (Fig. 3).
DISCUSSION
Obesity is caused by a genetic predis-
position and environmental and lifestyle
factors, including physical inactivity and
poor eating habits
23
. Physical inactivity and
obesity are associated with visceral fat accu-
mulation, leading to chronic low-grade in-
flammation and the pathogenesis of IR, MS,
DM2, cardiovascular diseases, and cancer
24,25
.
Total sedentary time and moderate-to-
vigorous physical activity have been reported
to be negatively correlated. Waist circumfer-
ence, body mass index, triglyceride level, and
plasma glucose level have also been reported
to decrease while the number of breaks in
sedentary time increased
1
. On that basis,
the present study aimed at determining the
impact of a modified HIIT on metabolic, an-
Table 3
Partial correlation between changes in leukocyte cells and changes in the anthropometric,
biochemical, and body composition variables.
Leukocyte cells Variables
ƿ
P
Δ of Total lymphocytes Δ of WC 0.491 0.053
Δ of granulocytes Δ of WC -0.514 0.041*
Δ of lymphocytes TCD8+ Δ of WC -0.612 0.007*
Δ of Glu 0.474 0.047*
Δ of DBP 0.458 0.056
Δ of c-LDL 0.617 0.006*
Δ of Total Cho. 0.460 0.055
Δ of TCD3+CD45RA+ Δ of c-LDL 0.959 0.010*
Δ of Total Cho. 0.941 0.017*
Δ of TCD3+CD45RA+CD45RO+ Δ of METS-IR 0.962 0.009*
Δ of TCD4+CD45RA+ Δ of ST -0.950 0.050*
Δ of BFM -0.974 0.026*
Δ of c-HDL 0.938 0.062
WC: waist circumference; Glu: glucose; DBP: diastolic blood pressure; c-LDL: Low-density cholesterol; Total Cho:
total cholesterol; ST: subcutaneous adipose tissue; BFM: body fat mass; c-HDL: high-density lipoprotein cholesterol.
p: p value adjusted by gender, age, and BMI (p<0.05).
348 Rodríguez-López et al.
Investigación Clínica 64(3): 2023
Fig. 3. Linear regression between changes in leucocytes cells and changes of the different variables.
High-Intensity Interval Training improves immunometabolism in sedentary obesity 349
Vol. 64(3): 338 - 354, 2023
thropometric, BC, and PBL measures in sed-
entary patients with OW and Ob.
HIIT has been proposed as a better-
suited activity for people with OW and Ob
than traditional continuous exercise
4
. Some
studies have reported a reduction in fasting
glucose, insulin, diastolic blood pressure
(DBP), and systolic blood pressure (SBP)
and improvements in insulin sensitivity af-
ter 16, 14, 12, or 2 weeks of HIIT
3, 26-29
. In
the present study, about 74% of participants
showed improvements in TG, Glu, TCho,
LDL-c, and HDL-c levels after training. Con-
cerning BC, other studies that implement-
ed HIIT in persons with OW or Ob for two
and 12 weeks, found a reduction in weight,
WC, fat mass, and BMI
27, 29
. In this study,
a significant statistical reduction was ob-
served only in WC in persons with OW, as
well as about 50% of participants showed de-
creased VAT (5.3±4.6cm
2
), ST (1.9±2.2%),
and BFM (1.7±1.5kg), and increased SMM
(1.3±1.6kg).
Although participants were untrained
people, they reached moderate intensity
during weeks 6 and 7 (62% of their inten-
sity percentage). The intensity percentage
increased as weeks progressed, observing a
significant difference between week 1 and
week 6 (p<0.05).
On the other hand, physical activity has
been often recognized as a powerful counter-
measure to inflammation
30
. A study carried
out with untrained young adults who par-
ticipated in HIIT for three days found that
the percentages of TCD4+, TCD8+, and
CD19+ lymphocytes increased significantly
after training
31
. Another study carried out
over two weeks with inactive persons with
OW or Ob revealed that training did not af-
fect the blood concentration of total lym-
phocytes (TL), monocytes, and neutrophils
27
. Both data do not coincide with those re-
ported in the present study, as it was found
that in persons with OW, TL, TCD3+, and
TCD8+ decreased (averages were similar
to those in persons with NW). On the other
hand, in individuals with Ob, TL decreased,
and granulocytes increased statistically, get-
ting closer to those values in persons with
NW. With these results, it can be observed
that only TL had the same behavior both in
individuals with OW and in those with Ob.
These data suggest differences in the mobili-
zation of leukocytes at the peripheral blood
level according to the nutritional status af-
ter physical activity.
In addition, it has been reported that
T lymphocytes and TCD8+ increase with
obesity
32, 33
and that they infiltrate adipose
tissue and promote the classical pro-inflam-
matory activity of M1 macrophages and the
production of pro-inflammatory cytokines.
These phenomena can trigger a metabolic
imbalance, such as an increase in Glu, TCho,
LDL-c, and TG and a decrease in HDL-c,
among others
34-36
. The finding in the present
study of diminished TL, TCD3+, and TCD8+
might indicate a decrease of the inflamma-
tory process at the peripheral blood level,
improving the metabolic profile, because
the improvement was found in the different
metabolic variables in a little more than 70%
of the participants, in addition, in different
correlations and linear regressions, it was
found a relationship between improvements
in lymphocyte subpopulations and both bio-
chemical and anthropometric variables.
Furthermore, in other studies, it has
been observed that monocytes, B cells, NK
cells, and T cells (CD4+ and CD8+) are
found in higher proportions in people with
obesity and provide a link between systemic
inflammation and IR
37-40
, which would guide
us to reiterate that having found some of
these cells decreased after physical activity
means an improvement of the inflamma-
tory process that is associated with IR and
metabolic alterations, representing a better
metabolic state for the participants.
On the other hand, in persons with
obesity, immunosenescent behavior has
been reported, similar to that appearing in
the elderly. This has been denominated as
“premature immunosenescence”, an imbal-
ance between senescent, naïve, and mem-
350 Rodríguez-López et al.
Investigación Clínica 64(3): 2023
ory cells that renders the individual with
obesity more susceptible to the disease
19,
43
. The specific increase in memory cells in
obese patients could somehow reflect what
some authors have pointed out about the
capacity for proliferation and activation of
memory cells, revealing the high degree of
chronic adaptive immune activation
41,42
,
which has been associated, as has already
been mentioned, with metabolic alterations
in these patients.
In this sense, it has been observed that
exercise may counteract immunosenescence
and its associated diseases by limiting the
accumulation of senescent T cells and re-
populating the blood with naïve T cells
30
,
mainly through promoting the expansion of
the naïve cell repertoire as a consequence of
the apoptosis of senescent T cells
44-47
, this
apoptotic process is thought to induce he-
matopoietic stem cells production in the
bloodstream, which may move to the thymus
and stimulate the development of naïve T
cells
30
. In the present study, in addition to
finding an increase in naïve cells after train-
ing (TCD3+ (p<0.05) in persons with OW),
a correlation between such an increase and
the reduction of total lymphocytes, IR and
LDL- cholesterol was observed. These results
suggest that this training could promote
immunometabolic regulation in these pa-
tients. Furthermore, it has been found that
senescent T lymphocytes are related to high
percentages of body fat
44, 46, 48
. It would be
valuable and interesting to investigate the
presence of senescent T cells in persons with
obesity.
Strengths, limitations and conclusions
Exercise is one of the therapies that ac-
company the treatment of obesity; However,
on some occasions, depending on the period
and the routine that is studied, it has been
observed that “there is no change”, but with
this work, we can realize that the physical
activity (modified HIIT with moderate inten-
sity, in this case) carried out, is influencing
the inflammatory process that triggers obe-
sity and, in turn, these changes were related
to immunometabolic improvements, thus
highlighting the relevance of this study.
Some of the study’s strengths were that
it was possible to implement an exercise
routine in a sedentary population; immu-
nometabolic changes were obtained in only
eight weeks of exercise. Also, the presence of
comorbidities (for example, dyslipidemias,
hypertriglyceridemias, hyperglycemia, MS,
among others) was detected and treated in
25% of the participants with exercise; All in-
ternational standards were followed to evalu-
ate the selected variables.
Certain limitations of the present study
were: The lack of analysis of other inflamma-
tion markers that could give us more infor-
mation about the inflammatory process be-
fore and after routine physical activity and
the voluntary desertion of some patients due
to the problem of adherence to a routine in
sedentary people.
In conclusion, this study reports that
an eight-week modified HIIT program
brought about positive changes in peripher-
al lymphocyte subpopulations in sedentary
individuals with OW or Ob, as it observed
a reduction in TL and TCD8+ and an in-
crease in naïve cells, bringing the values
closer to those in persons with NW. These
changes correlated with healthier meta-
bolic variables. Also, differential leukocyte
changes were observed according to BMI.
These results represent novel knowledge
about the positive effects of HIIT, not only
regulating whole-body metabolism but also
regulating immunomodulatory effects with
anti-inflammatory benefits. All these re-
sults reinforce the benefits of HIIT as an ex-
ercise strategy to promote the regulation of
immunometabolism.
As shown in this study, exercising is es-
sential, and obese patients should be made
aware that they should make changes in their
lifestyle in general, particularly in terms of
having a more active life. For this reason, it
is essential to continue conducting studies
of this nature.
High-Intensity Interval Training improves immunometabolism in sedentary obesity 351
Vol. 64(3): 338 - 354, 2023
ACKNOWLEDGMENTS
The authors acknowledge LN María
Magdalena Rodríguez-Magallanes for techni-
cal support, as well as the National Council
of Science and Technology (CONACYT, Méxi-
co) for a postgraduate studies scholarship
awarded to Carmen Paulina Rodríguez-López
(371434).
Funding
None
Conflict of interest
None
ORCID numbers
Carmen Paulina Rodríguez-López
(CPRL): 0000-0001-8226-4971
María Cristina González- Torres
(MCGT): 0000-0002-3778-422X
Oralia Nájera-Medina (ONM):
0000-0003-2166-3770
Authors contribution
CPRL: research design, perform the in-
terventions and experiments, data analysis,
interpretation of the results, preparation,
and writing of the article, elaboration of fig-
ures and tables.
ONM: research design, data analysis, in-
terpretation of the results, preparation, and
writing of the article.
MCGT: interpretations of the results,
preparation, and writing of the article.
All authors approved the final version of
the article for publication.
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