In the article titled “Impact of Yoga and Meditation on Cellular Aging in Apparently
Healthy Individuals: A Prospective, Open-Label Single-Arm Exploratory Study” [1],
there were a number of language errors, due to publisher error. The corrected version
of the article is shown below:
Abstract
This study was designed to explore the impact of a yoga- and meditation-based lifestyle
intervention (YMLI) on cellular aging in apparently healthy individuals. During this
12-week prospective, open-label, single-arm exploratory study, 96 apparently healthy
individuals were enrolled to receive YMLI. The primary endpoints were assessment of
the change in levels of cardinal biomarkers of cellular aging in blood from baseline
to week 12, which included DNA damage marker 8-hydroxy-2′-deoxyguanosine (8-OH2dG),
oxidative stress markers reactive oxygen species (ROS), and total antioxidant capacity
(TAC), and telomere attrition markers telomere length and telomerase activity. The
secondary endpoints were assessment of metabotrophic blood biomarkers associated with
cellular aging, which included cortisol, β-endorphin, IL-6, BDNF, and sirtuin-1. After
12 weeks of YMLI, there were significant improvements in both the cardinal biomarkers
of cellular aging and the metabotrophic biomarkers influencing cellular aging, compared
to baseline values. The mean levels of 8-OH2dG, ROS, cortisol, and IL-6 were significantly
lower and mean levels of TAC, telomerase activity, β-endorphin, BDNF, and sirtuin-1
were significantly increased (all values p < 0.05) post-YMLI. The mean level of telomere
length was increased but the finding was not significant (p = 0.069). YMLI significantly
reduced the rate of cellular aging in an apparently healthy population.
1. Introduction
In the last decade there has been a significant increase in complex lifestyle diseases
like depression, diabetes mellitus (DM), cardiovascular diseases (CVD), cancer, and
infertility. These diseases are strongly associated with accelerated cellular aging
[1, 2] and have become the bane of modern society [3–5]. Within a homogeneous sample
of an apparently healthy adult population, biomarkers have been defined recently [6]
to characterize the complex processes of an accelerated aging phenomenon. Although
we do not have any gold standard biomarker to monitor healthy aging, based on the
current knowledge of putative biomarkers, the cardinal biomarkers of cellular aging
and metabotophic biomarkers that can influence them have become the focus of the latest
translational research to develop interventions to prevent chronic lifestyle diseases.
The cardinal biomarkers of cellular aging include DNA damage, telomere length attrition,
and oxidative stress (OS) [7]. DNA damage causes genomic instability, which is responsible
for cellular dysfunction in the pathogenesis of lifestyle diseases [8–10]. OS is the
most important cause of DNA damage. Although many different oxidative DNA damage (ODD)
products have been identified, 8-OH2dG (8-hydroxy-2′-deoxyguanosine), a highly mutagenic
oxidative DNA adduct, has been the subject of intensive study and is a definitive
biomarker of DNA damage [11]. Telomere attrition is due to altered telomere metabolism
involving a decrease in telomerase enzyme activity and an increase in OS. It contributes
to genomic instability and is associated with aging and lifestyle diseases [12].
Oxidative stress, an imbalance between prooxidants and antioxidant defense mechanisms,
becomes pathological at both extremes of the physiological range needed for normal
cellular functions. It is involved in the pathogenesis of complex lifestyle and chronic
diseases [13], including depression [14], obesity [15], and infertility [16, 17],
the leading public health problems.
Several metabotrophic blood biomarkers influencing cellular aging include biomarkers
of stress and inflammatory response, neuroplasticity, and longevity. Sustained stress
responses due to chronic stress stimuli cause constantly increased cortisol levels
[18], which lead to systemic tissue abnormalities like increased adiposity and neurodegeneration.
The level of stress responsiveness (cortisol levels) can be a biomarker for predicting
susceptibility to lifestyle diseases [19]. Accelerated aging is characterized by a
chronic, low-grade inflammation (“inflammaging”). Inflammaging is a highly significant
risk factor for most chronic lifestyle diseases [20] and is a potential modifiable
target [21]. IL-6 is the most prominent cytokine in inflammaging and is both a marker
of inflammatory status and a hallmark of chronic morbidity [22]. Impaired neuroplasticity
due to accelerated aging can have negative influence across the entire lifespan [23].
BDNF is a major regulator of neuroplasticity [24], which may be increased in specific
regions of the brain by various interventions [25]. Health span and longevity are
influenced by several factors. Sirtuin-1 (SIRT1), a histone deacetylase (HDAC), is
prominent among them and recently has become a target for various interventions [26].
It systemically influences nutrition and energy metabolism and centrally has a role
in circadian rhythm, survival against stress [27] and neuronal plasticity [28].
A variety of interventions have been studied [29, 30] to determine their influence
on preventing lifestyle diseases and promoting health and longevity. They include
treatments targeting specific hallmarks of aging, namely, physical exercise [31],
nutrition, caloric restriction [32], and antioxidants [33]. However, no single intervention
is shown to be an effective preventive and therapeutic strategy for modern complex
lifestyle diseases and to provide comprehensive benefits for delaying or reversing
accelerated aging. Therefore, further research is needed to find optimum interventions
for population at risk of lifestyle diseases. Yoga is an emerging integrative health
discipline, which can positively modulate mind and body [34] and has been shown to
improve the clinical profile of patients with various pathologies [35] including depression,
obesity, hypertension, asthma, type II diabetes, and cancer. However, recent reviews
on yoga suggest that potential underlying mechanisms need to be further explored [36].
Studies on biomarkers of disease and health in yoga-based interventions are limited
and they have only highlighted diabetic and lipid profiles [37, 38], stress and inflammatory
markers [39, 40] and neuroimaging correlates [41], in populations with specific medical
conditions. Evidence is lacking regarding the efficacy of yoga lasting a short duration
of 3 to 12 weeks in improving the biomarkers of cellular aging in apparently healthy
people. Thus, the present study was designed to evaluate the impact of a yoga- and
meditation-based lifestyle intervention (YMLI) on cellular aging and longevity by
analyzing cardinal and metabotrophic biomarkers in the peripheral blood of apparently
healthy subjects.
2. Materials and Methods
2.1. Study Design and Participants
Ninety-six apparently healthy people were enrolled in this 12-week prospective, open-label,
single-arm exploratory study, from August 2015 to May 2016, designed to explore the
impact of YMLI on cellular aging. The key inclusion criteria were male or female aged
30–65 years and leading an unhealthy modern lifestyle. The key exclusion criteria
were inability to perform the yogic exercises due to any physical challenges and those
with recent changes in lifestyle during the last 3 months. The study was initiated
after ethical clearance (ESC/T-370/22-07-2015) and the registration of the trial with
the Clinical Trial Registry of India (CTRI REF/2014/09/007532).
2.2. Procedure
2.2.1. Yoga- and Meditation-Based Lifestyle Intervention (YMLI)
Eligible subjects were enrolled in the study after screening and baseline characteristics
were recorded. Participants underwent a 12-week pretested YMLI program comprising
theory and practice sessions [42, 43]. YMLI is designed to be an integrative health
strategy incorporating the classic components of yoga including asanas (physical postures),
pranayama (breathing exercises), and dhayna (meditation), which are derived from a
mix of Hatha yoga and Raja yoga. The YMLI for the current study was suitably modified
for apparently healthy subjects. YMLI program included sessions five days per week
for 12 weeks. For the first two weeks, the sessions were held at the integrated health
clinic (IHC), AIIMS, New Delhi, and taught by registered, specialized yoga instructors
(educational qualifications include Bachelor of Naturopathy and Yoga Sciences and
P.G. Diploma in Yoga Therapy). The remaining 10 weeks were home based. Monitoring
of compliance of the home-based YMLI was through maintenance of a diary and telephonic
contact. The details of the activities in a day during the YMLI program are given
in Table 1. Each session in YMLI included a set of asanas, pranayama, and dhayna for
approximately 90 minutes. This was followed by an interactive lecture (only during
the first two weeks of YMLI at IHC) on lifestyle, lifestyle diseases, and importance
of their prevention for 30 minutes.
2.2.2. Laboratory Procedures
During this 12-week study the participants were evaluated for various biomarkers on
day 0 and week 12. Fasting venous blood samples (5 mL) were collected and divided
into two parts. One part was allowed to clot and the serum was separated within 30 minutes
and the other part was transferred to heparinized/EDTA vials and was centrifuged at
2000g for 15 minutes at 4°C. Both serum and plasma were stored at −80°C until analyzed.
ROS detection was done by chemiluminescence assay (Berthold detection luminometer,
USA). Peripheral blood leukocyte telomere length was measured by qPCR and telomerase
activity was determined by using a telomerase assay kit (Roche, Switzerland), as per
the manufacturer's protocol. 8-OH2dG was estimated in white blood cell DNA (Cayman's
EIA kit). ELISA kits were used for levels of TAC (Cayman Chemical, Ann Arbor, USA),
cortisol (DRG Diagnostic, Germany), β-endorphin (Phoenix Pharmaceuticals, Inc.), IL-6
(Gen-Probe, Diaclone Diagnostic, France), BDNF (Raybiotech, Inc), and sirtuin-1 (Quayee
Bio-Technology). Quality control assays for biomarkers and validation were performed.
2.2.3. Endpoints
The primary endpoint was to assess the change in levels of cardinal biomarkers of
cellular aging from baseline to week 12. The biomarkers included the following: 8-OH2dG,
ROS, and TAC (markers of OS and ODD) as well as telomere length and telomerase activity
(telomere attrition markers). The secondary endpoints were assessment of metabotrophic
blood biomarkers associated with cellular aging, which included cortisol, β-endorphin,
IL-6, BDNF, and sirtuin-1 from baseline to week 12.
2.3. Statistical Analysis
Data were analyzed using SPSS 20 (IBM Corp, Armonk, NY). Descriptive statistics are
reported as means and standard deviations. Changes in outcome variables were analyzed
using paired-samples t-tests. Exploratory analysis included comparisons for within
gender subgroups using paired-sample t-tests. Significance was accepted at p < 0.05.
3. Results
The flow diagram of participant details is provided in Figure 1. Of 96 subjects, 94
subjects were assessed for impact analysis. Two subjects were excluded from the analysis
due to poor compliance to the program. Baseline sociodemographic characteristics are
shown in Table 2.
After 12 weeks of YMLI, there was significant improvement in both cardinal and metabotrophic
biomarkers of cellular aging compared to baseline values (Table 3). The mean levels
of 8-OH2dG and ROS were significantly lower and mean levels of TAC and telomerase
activity were significantly increased (all values p < 0.05). The mean level of telomere
length was increased, but this finding was not significant (p = 0.069). The mean levels
of cortisol and IL-6 were significantly lower and mean levels of β-endorphin, BDNF,
and sirtuin-1 were significantly increased (all values p < 0.05).
A few differences were noted in the gender subgroup analysis. Only the male subgroup
showed a significant decrease in the levels of IL-6 and a more marked reduction in
cortisol levels (males p = 0.001; females p = 0.036). After 12 weeks of YMLI, we also
noted significantly reduced BMI in the study population (p < 0.01).
4. Discussion
The results of this study highlight the positive impact of YMLI on biomarkers of cellular
aging and in promoting cellular longevity through changes in both cardinal and metabotrophic
biomarkers. The findings suggest that the impact is mediated through improvement in
genomic stability, telomere metabolism, and balance of cellular oxidative stress,
well-regulated stress and inflammatory responses, and increase in neuroplasticity
and nutrition sensing.
Genomic stability is central to cellular longevity and disease-free youthful healthy
life and the findings from our study suggest the reduction of genomic instability
(decreased levels of 8-OH2dG) by YMLI. Unhealthy social habits (smoking, excess alcohol
intake, etc.), sedentary lifestyle, exposure to environmental pollutants, and intake
of processed and nutritionally depleted food have taken a toll on human health, with
the onset of lifestyle diseases at a much younger age [3–5]. These environmental and
lifestyle factors are responsible for genomic instability [10]. DNA damage to both
the mitochondrial and nuclear genome from endogenous as well as exogenous insults
results in accumulation of genetic aberrations and genome hypermutability [8–10].
This is mainly due to aberrant DNA damage response (DDR) pathway, which is essential
for DNA repair and for monitoring genomic integrity. Deficient DNA repair triggers
systemic effects to promote pathological aging [10]. The reduction of DNA damage by
YMLI suggests the potential of yoga in activating the DDR pathway to repair genomic
damage and improve genomic stability, and changes in metabotrophic factors seen in
the study may be associated with these benefits.
Maintaining telomere length through regulation of telomere metabolism contributes
to genomic stability, and the reduction in telomere attrition (increase in telomere
length and telomerase activity levels) shown by our study after YMLI suggests the
potential for yoga in telomere metabolism and cellular longevity. Telomeres, which
serve as a biological clock, are highly conserved hexameric repeats and maintaining
their length is vital for cellular longevity. Telomerase is an important regulator
of telomere length and accurate regulation of its activity, and a correct telomere-telomerase
interaction, is important to precisely safeguard telomere length and prevent telomere
attrition [44]. ODD is prominent among the factors that can adversely affect telomere
length [45]. Rapid telomere attrition due to ODD is associated with senescence and
related disease conditions [46, 47]. Improved telomere metabolism after YMLI seen
in the study may contribute to genomic stability. More research is needed to explore
the mechanisms of how yoga and meditation can positively modify telomere metabolism.
Our study suggests an improvement in maintenance of balance in cellular oxidative
stress (decrease in ROS and increase in TAC) caused by YMLI. Supraphysiological ROS
levels are due to endogenous and exogenous factors like smoking, excess alcohol consumption,
exposure to electromagnetic radiation, infection, xenobiotic exposure, and psychological
stress [48]. Even the levels of ROS below physiological limits are deleterious to
normal cellular function and maintaining OS at physiological levels is important for
cellular longevity. Increased OS causes damage to all molecules, including damage
to DNA and telomeres. It also affects signal transduction and gene transcription by
causing genome-wide hypomethylation [49] and thus causes changes in the epigenome.
Regulation of cellular oxidative stress within physiological limits after YMLI suggests
the potential of this intervention in protecting cells from OS-induced DNA damage
and telomere attrition and in reversing epigenetic changes, which are accumulated
due to an unhealthy lifestyle and adverse environmental conditions. Other studies
[50] support these findings and have shown reduced OS upregulation of telomerase activity
and decreased ODD after YMLI. To combat OS people use antioxidants without monitoring
ROS levels resulting in reductive stress [51], unlike in YMLI which regulates ROS
levels so that no redox-sensitive physiological functions are impaired.
Modern lifestyle and associated psychological stress have complex interactions with
habits, environmental conditions, and medical interventions to cause accelerated cellular
aging, which adversely affect our mental, physical, and reproductive fitness [3–5].
Improved cellular longevity after YMLI suggests the potential role of yoga in promoting
this fitness. While psychological stress has a major effect on the mind, contributing
to an increased prevalence of neuropsychiatric disorders including depression, abnormal
fat accumulation is a major somatic manifestation contributing to increased prevalence
of metabolic syndrome and all the diseases that come under this umbrella including,
obesity, DM, and CVD [52]. Other peripheral manifestations of unhealthy modern lifestyle
include aging of gonads leading to infertility [53] and recurrent pregnancy loss.
Previous studies have demonstrated the clinical benefits of yoga and meditation in
all these medical conditions [35]. Dada et al. have shown that YMLI can reduce testicular
aging and result in significant upregulation in telomerase activity and decline in
seminal OS and ODD [8]. The ongoing studies in our laboratory on the impact of yoga
and meditation have provided significant evidence for the reversal of cellular aging
in subjects prone to accelerated aging due to depression. Microarray (Agilent 8 ×
60k Microarray kit) and analysis of gene expression pre- and post-YMLI showed decreased
IL6, IL10, and MAP10 and increased IL2 and IL4 [8, 54, 55]. Improved cellular longevity
seen in our study after YMLI suggests that changes in both cardinal and metabotrophic
biomarkers of cellular aging may be a mechanism for preventing chronic lifestyle diseases.
Our study suggests that the changes in metabotrophic factors, which include increase
in levels of β-endorphin, BDNF, and sirtuin-1 and decrease in levels of cortisol and
IL-6, and the cellular processes involving them, may have important roles in the reversal
of cellular aging and improving cellular longevity after YMLI.
Improvements in stress and inflammatory response in our study after YMLI may be mediated
by changes in cortisol, β-endorphin, IL-6, and other factors, with regulation by changes
in the brain through the hypothalamic-pituitary-adrenal (HPA) axis. The response may
involve regulation of adaptive pathways, including integrated stress response (ISR)
[18] that activates eukaryotic translation initiation factor 2 alpha (eIF2α), that
promote cellular recovery driving signaling toward cell survival and longevity. The
response may lead to decreased OS and a reversal of the senescent secretory phenotype
of cells, including cells in the brain, adipose tissue, endothelium, and gonads. Changes
in secretory phenotype include decreased IL-6 [56], increased BDNF, and sirtuin-1
[57]. These regulated factors may lead to balance in OS and cellular longevity and
contribute to tissue revival throughout the body from neuroplasticity in CNS to gonads,
vessels, and muscles in the periphery. Secretory phenotype from somatic cells provides
regulatory feedback to brain [58], which completes the vicious cycle of regulation
between mind and body. Neurodegeneration is associated with the pathogenesis of several
neuropsychiatric conditions and neuroplasticity has a central role in their management
and for vitality. Increased BDNF, sirtuin-1, and β-endorphin and decreased cortisol
each decrease cellular aging in brain, decrease neurodegeneration and increase neuroplasticity
[23]. Increased cellular longevity and increased neuroplasticity may be a mechanism
for alteration of gray matter volume in different regions of the cerebral cortex [59],
increased mindfulness [60], and several other complex processes [55, 61] involved
in reduction of stress and depression after yoga and meditation. Regulated mind-body
communications may lead to minimization of subclinical inflammation and activation
of nutrition and energy-sensing pathways promoting longevity, where a decrease in
IL-6 and an increase in sirtuin-1 play a prominent role, respectively. Previous studies
have demonstrated an increase in sirtuin-1 levels after interventions with caloric
restriction [62]. Our study is the first to document an increase in sirtuin-1 levels
independent of caloric restriction after practicing yoga. These improved processes
may result in delaying onset and slowing down progression of diseases associated with
accelerated cellular aging.
The impact of the intervention in both genders was assessed separately since men and
women respond differently to day-to-day stress [63]. Interestingly, the gender subgroup
analysis showed that reductions in cortisol and IL6 levels were more pronounced in
male than in female subjects. No significant gender differences were seen in the other
biomarkers. Phase of the menstrual cycle should be taken into consideration, since
some biomarker levels are known to vary with different phases of the menstrual cycle
[64, 65]. Our study showed a significant decrease in BMI in apparently healthy subjects,
which came into the normal range (23.64 ± 3.55) from a baseline overweight range (26.30
± 3.40). While the latest research [66] suggests people with a mean BMI of 27, who
are overweight by the current classification of obesity, are likely to survive longest
in a Western population, similar data is not available for the Indian population.
Therefore, our findings need to be interpreted cautiously.
Stratification of cases was not done in this study to do a subgroup analysis due to
the small sample size.
Lifestyle is an integrated entity, and an intervention like YMLI that has an overall
positive influence on our health appears most useful versus changing only one aspect
at a time, as is seen by the action of certain drugs. Yoga is holistic and a mind-body
medicine and is more beneficial and advantageous than individual interventions like
physical exercise, caloric restriction, and antioxidants. The practice of yoga and
physical exercise are different entities; the former results in energy conservation
with economy of energy expenditure for mental and physical benefits, and the later
results in energy expenditure more for physical exertions and metabolic needs, as
is evident from a study that showed exercise causes erratic changes in biomarkers
and results in OS [67] while meditation brings about uniform biomarker and behavioral
changes and improvement in cognition and decrease OS [68]. Therapeutic antioxidants
can only decrease ROS rather than regulating it and may paradoxically shorten lifespan
[69] due to an imbalance in ROS-mediated immune responses [70]. YMLI regulates ROS
rather than simply lowering them by balanced stress-related processes and appropriate
gene expression [71]. The only limitation of our study is that it is a single-arm
proof-of-concept study and did not include controls. It is important to adopt a lifestyle
that slows the decline in health by reversing or delaying accelerated aging due to
unhealthy lifestyles. The biomarkers of cellular aging can form the basis for determining
the risk of chronic lifestyle diseases and the efficacy and usefulness of interventions
to decrease disease risk. Hence, the findings from this study are supportive of YMLI
as having significant clinical utility especially in the prevention of and management
of complex multifactorial diseases and reducing the rate of functional decline with
aging.
5. Conclusion
Though we cannot change our biology or chronological age we can definitely reverse/slow
down the pace at which we age by adopting YMLI. This is the first study to demonstrate
improvement in both cardinal and metabotrophic biomarkers of cellular aging and longevity
in an apparently healthy population after a yoga- and meditation-based lifestyle intervention.
Our health and the rate at which we age entirely depends on our choices. Making yoga
and meditation an integral part of our lifestyle may hold the key to delay aging or
aging gracefully, prevent the onset of multifactorial complex lifestyle diseases,
promote mental, physical, and reproductive health, and prolong youthful healthy life.