|


















Ugrad Advising Appts
College of Education
MSU
Copyright ©
Michigan State University
| |
| |
Biomarkers and
Genetics Laboratory
The primary focus of
the Biomarkers and Genetics Laboratory (BAGL) is to gain a better
understanding of the genesis of the metabolic syndrome during childhood and
adolescence. In other words, we are interested in the causes and
consequences of obesity and the emergence of Type 2 diabetes and vascular
disease during childhood and adolescence.
The obese child
generally displays an adverse cardiovascular disease (CVD) risk factor
profile that includes elevated blood pressure, glucose, and triglycerides
and lowered high-density lipoprotein-cholesterol. This constellation of
obesity and CVD risk factors has been termed the metabolic syndrome. In
addition, new emerging risk factors related to hemostasis, fibrinolysis, and
inflammation have been identified in the obese child and some of these
biomarkers are actually secretory proteins of the adipocyte – known as
adipocytokines or adipokines. Several factors may contribute to the
emergence of the metabolic syndrome in adolescence including genetics,
reduced daily energy expenditure, low aerobic fitness, and dysregulation of
the hypothalamic-pituitary-adrenal or sympathomedullary axis during puberty.

It is important to
understand these associations given the potential roles of genetics,
habitual physical activity, aerobic fitness, and stress on the etiology of
the metabolic syndrome, Type 2 diabetes, and CVD during childhood growth and
puberty. The long-term goal of this research is to elucidate the mechanisms
of the metabolic syndrome through the complex interactions of genetics,
environmental factors (particularly stress, exercise, and diet), and the
neuro-endocrine, hormonal, metabolic, hemostatic and inflammatory systems in
the growing and maturing obese child. An understanding of these
complex interactions in the obese adolescent may provide a better
understanding of the etiology of the metabolic syndrome, Type II diabetes
and atherosclerosis and the prevention and treatment of these clinical
disorders in the obese adolescent.
Lab Director
Joe
Eisenmann, Ph.D.
3 IM Sports
Circle
Michigan State University
East Lansing, MI 48824
(517) 432-5105
jce@msu.edu
Current Projects
 |
Genetics, physical
activity, and obesity-hypertension in young children.
The objective of this study is to examine the longitudinal development of
the adiposity and BP phenotypes in young children taking into account
physical activity and the angiotensinogen converting enzyme (ACE)
polymorphism. We chose to study ACE polymorphisms since it is a
positional candidate gene that may have
pleiotropic effects on adiposity and BP.
In the context of human growth, it has been
suggested that a master gene has pleiotropic control over somatic growth,
obesity and BP. Given the potential roles of adiposity, physical
activity and genes and their interactions on the etiology of the
hypertension during early life, it is critical that we increase our
understanding of the genesis of obesity and hypertension and develop
appropriate prevention and treatment strategies. This project is
currently funded by the American Heart Association. Collaborators
include: Dr. Kate Heelan, University of Nebraska-Kearney; Dr. Greg Welk,
Iowa State University; Dr. Max Rothschild, Iowa State University; Dr. Adam
Baxter-Jones, University of Saskatchewan. |
 |
Genetics, adolescent
fatness and fitness as predictors of adult metabolic syndrome.
In this study, we are addressing if adolescent growth is related to
subsequent adult disease by following subjects from the Saskatchewan
Growth and Development Study (SGDS, 1964-1973) who are now approaching the
age of 50 years of life, which is about the time that the clinical
manifestations of CVD and type 2 diabetes occurs. Given the longitudinal
design of the SGDS we can also investigate the influence of longitudinal
growth trajectories during adolescence on adult health outcomes; unlike
cross-sectional associations between one-time adolescent and adult
measures used in previous studies, the proposed study design allows us to
calculate growth trajectories which incorporate change over the entire
period. This work will identify potential antecedents in early life that
affect the metabolic syndrome. Funding for this project is from the
Canadian Institutes of Health Research (Co-investigator with Dr. Adam
Baxter-Jones, University of Saskatchewan). |
 |
Physical activity,
stress, and new emerging risk factors.
The objective of this project is examine the inter-relationships among
energy expenditure, aerobic fitness, stress, and emerging risk factors in
highly active runners, obese, and non-obese adolescent boys. Forty 12-20
yr old males were assessed for physical activity, aerobic fitness, stress,
fatness, and emerging risk factors. Outcomes of this research will be
important in understanding the complex physiological interactions that
lead to the metabolic syndrome, and the prevention and treatment of the
obese adolescent. |
 |
Physical activity,
stress, and the metabolic syndrome.
The objective of this study is to gain an understanding of the role of
stressors on the genesis of the metabolic syndrome during puberty. This
project has two specific aims: 1) Examine the stress response to
psychological and physical perturbations in obese and non-obese
adolescents. In this study, measurement of salivary cortisol will be used
as an indicator of HPA axis activity and BP and heart rate will be used as
indicators of the SAM axis. We hypothesize an exaggerated stress response
in obese adolescents compared to non-obese adolescents. 2) Examine the
relationships among energy expenditure, cortisol, and atherosclerotic risk
factors in obese and non-obese adolescents. We hypothesize a direct
relationship between baseline cortisol levels and atherosclerotic risk
factors and more specifically we hypothesize that physical activity will
modify the relationship between cortisol and atherosclerotic risk
factors. This research was supported by the Center for Designing Food and
Improving Nutrition, Iowa State University through the U.S. Department of
Agriculture. |
 |
Effects of physical
activity on the metabolic syndrome during postnatal development in mice
selectively bred for high capacity running: an ontogenetic model of the
metabolic syndrome.
An alternative to longitudinal studies of human children and adolescents
is the postnatal animal model. We are beginning collaborations with Dr.
Ted Garland (University of California-Riverside) to use a novel animal
model to examine the unique and combined contributions of genetics and
physical activity on the postnatal development of the metabolic syndrome.
Here, we will use mice that have been
selectively bred to run voluntarily on wheels almost 200% more than
non-selected lines (controls). The objective of this study is to
gain an understanding of the role of genetics and physical activity
on the genesis of the metabolic syndrome during postnatal
development using a novel animal model. This project has two specific
aims: 1) Examine the ontogeny of the metabolic syndrome in two strains of
mice – one selectively bred for high levels of
voluntary exercise and a control
line. 2) Examine the effects of physical
activity (access to a running wheel) on the ontogeny of the
metabolic syndrome in both strains of
mice. This work is currently supported from a Michigan State University
Seed Grant. |
Related Publications
 |
M Holmes, JC
Eisenmann, D Gentile,P Ekkakski.
Physical activity,
stress and metabolic risk score of adolescent males. J Phys Activity
Health (in press). |
 |
JC
Eisenmann. Aerobic fitness, fatness, and the metabolic syndrome in
children and adolescents. Acta Pediatr (in press). |
 |
JC Eisenmann
and K Tolfrey.
Genetics and pediatric
exercise science: a commentary and review. Pediatric Exercise Science
(in press). |
 |
K DuBose, JC
Eisenmann, JE Donelly.
Aerobic
fitness attenuates the metabolic syndrome score in normal weight,
at-risk-for-overweight, and overweight children Pediatrics (in
press). |
 |
JC
Eisenmann, GJ Welk, MA Ihmels, J Dollman.
Fitness, fatness and
cardiovascular disease risk factors in children and adolescents.
Medicine Science Sports Exercise 39:1251-1256, 2007. |
 |
JC
Eisenmann, K DuBose, JE Donnelly.
Fatness, fitness, and
insulin resistance among 7-9 yr old children. Obesity 15 2135-2144,
2007. |
 |
JC Eisenmann, GW Welk, EE Wickel, and SN Blair.
Combined
influence of cardiorespiratory fitness and body mass index on
cardiovascular disease risk factors among 8-18 year old youth: The
Aerobics Center Longitudinal Study International Journal of Pediatric
Obesity 2: 66-72, 2007. |
 |
JC Eisenmann, P Ekkekakis, M Holmes.
Sleep
duration and overweight in children and adolescents. Acta Pediatrica
95:956-963, 2006. |
 |
JC Eisenmann. Insight
into the causes of the recent secular trend in pediatric obesity: common
sense does not always prevail for complex, multi-factorial phenotypes.
Preventive Medicine 42:329-335, 2006. |
 |
JC Eisenmann
J Wrede, K Heelan.
Associations between
adiposity, family history of CHD and blood pressure in 3-8 yr old
children. Journal of Human Hypertension 19:675-681, 2005. |
 |
J
C Eisenmann, P T Katzmarzyk, L Perusse, A Tremblay, J-P Després and
C Bouchard
Aerobic fitness, body mass index, and CVD risk factors among adolescents:
the Quebec Family Study. Int J Obes Relat
Metab Disord 29: 1077-1083, 2005. |
 |
JC
Eisenmann, EE Wickel, GJ Welk, SN Blair.
Relationship between adolescent fitness and fatness and cardiovascular
disease risk factors in adulthood: the Aerobics Center Longitudinal Study.
American Heart Journal 149:46-53, 2005. |
 |
JC
Eisenmann, EE Wickel, GJ Welk, SN Blair.
Stability of cardiovascular disease risk factors in from adolescence into
adulthood: the Aerobics Center Longitudinal Study. American Journal of
Human Biology 16:690-696, 2004. |
 |
K. Garcia,
J.C. Eisenmann, R.T. Bartee.
Does a family history
of CHD modify the relationship between physical activity and blood
pressure in young adults? European Journal of Cardiovascular
Rehabilitation and Prevention
11(3):201-206, 2004. |
 |
J.C. Eisenmann.
Physical activity and cardiovascular disease risk factors in children and
adolescents: an overview. Canadian Journal of Cardiology
20(3):295-301, 2004. |
 |
J.C. Eisenmann.
Secular trends in variables associated with the metabolic syndrome among
North American children and adolescents. American Journal of Human
Biology, 15:786-794, 2003. |
 |
J.C.
Eisenmann and R.M. Malina.
Changes in
subcutaneous adipose tissue in young distance runners and association with
blood lipoproteins. Annals of Human Biology, 29:389-397, 2002. |
 |
J.C. Eisenmann. Blood
lipids and lipoproteins in the child and adolescent athlete. Sports
Medicine, 32(5):297-307, 2002. |
|
|