Summary

唾液を収集し、家族介護者を経由して高齢者を居住する虚弱コミュニティ唾液コルチゾールおよびα-アミラーゼの測定

Published: December 18, 2013
doi:

Summary

We demonstrate: (1) procedures for collection of salivary samples in cognitive impaired older adults by family caregivers in the home setting, (2) procedures for measuring stress activity via salivary cortisol and alpha amylase, and (3) representative profiles. Protocols that allow researchers to study stress-linked processes advance our understanding of biological sensitivity and susceptibility.

Abstract

Salivary measures have emerged in bio-behavioral research that are easy-to-collect, minimally invasive, and relatively inexpensive biologic markers of stress. This article we present the steps for collection and analysis of two salivary assays in research with frail, community residing older adults-salivary cortisol and salivary alpha amylase. The field of salivary bioscience is rapidly advancing and the purpose of this presentation is to provide an update on the developments for investigators interested in integrating these measures into research on aging. Strategies are presented for instructing family caregivers in collecting saliva in the home, and for conducting laboratory analyses of salivary analytes that have demonstrated feasibility, high compliance, and yield quality specimens. The protocol for sample collection includes: (1) consistent use of collection materials; (2) standardized methods that promote adherence and minimize subject burden; and (3) procedures for controlling certain confounding agents. We also provide strategies for laboratory analyses include: (1) saliva handling and processing; (2) salivary cortisol and salivary alpha amylase assay procedures; and (3) analytic considerations.

Introduction

The theoretical perspective guiding lifespan developmental science emphasizes the need to integrate biological, behavioral, social, and contextual factors into the study of health and behavior1. Contemporary theoretical models champion the notion that individual differences in biological sensitivity and susceptibility to contextual factors may moderate risk versus resilience, and can forecast morbidity and mortality in vulnerable populations. Considerable research attention has focused on these issues early in life development1, but only recently have investigators been able to test the core ideas in studies with medically and cognitively frail older adults2-4. One reason for this trend is the development of procedures to noninvasively measure differences in neurobiological activity including the hypothalamic-pituitary-adrenal (HPA) axis and autonomic nervous system (ANS) within and across individuals via oral fluids (saliva)5,6.

Salivary measures can allow for the collection of normative longitudinal data, to compare changes between different treatment groups, to compare effectiveness of interventions, or can be extended to include measurement of coregulation or activity between multiple individuals. The data obtained from these measures can shed light on stress-linked biological processes in health conditions common in older adults including cancer, heart disease or neurocognitive disorders7. Saliva has received growing attention as a biospecimen due to the perceptions of sample collection as an easy to learn, inexpensive, minimally invasive, and acceptable8. Nonetheless, the conventional methods of collection requiring participants to drool through a straw into a small tube have been shown to be too complicated or undesirable for older, frail participants. New methods are required that can standardize the preanalytical phase of collection and processing to deliver the most accurate and meaningful results. The field of salivary bioscience is advancing rapidly and the purpose of this presentation is to provide an update of developments and a practical roadmap for investigators interested in integrating these measurement approaches into research on aging. In this protocol we demonstrate (1) procedures for collection of salivary samples in cognitive impaired older adults by family caregivers in the home setting, (2) the procedures for measuring HPA axis and ANS activity via salivary cortisol and salivary alpha amylase (sAA), and (3) representative individual differences in salivary cortisol and sAA data.

Protocol

1. Recruitment Obtain appropriate Institutional Review Board approval of collection protocol with special attention to consenting subjects with impaired capacity and the collection of biological specimens9-10. Exclude participants with potential for blood leakage into saliva by assessing oral health (i.e. "Did you observe bleeding gums in the past two days?")11. 2. Preparation of Saliva Collection Supplies Pri…

Representative Results

The protocol is meant to provide one example of how salivary biomeasures can be collected in the community setting. The procedures are designed to measure the diurnal profile of salivary alpha amylase and salivary cortisol concentrations (Figure 2). Analytic Strategy Cortisol results have been shown to be positively skewed. Therefore it is suggested to use log transformation to the data to yield a normal distribution. Several strategies are available t…

Discussion

To advance our understanding of the meaning of individual differences in biological sensitivity and susceptibility in frail older adults investigators will need to engage caregivers in the collection of biological specimens. These collection protocols need to be minimally invasive, easy to accomplish, and yield quality specimens. Since one major challenge is ensuring that caregivers collect the samples at the correct time family caregivers designated as saliva collectors should be screened for ability to understand writt…

Disclosures

The authors have nothing to disclose.

Acknowledgements

Study funded by NINR, K23NR012017-01A1 Adrenocortical Response and Neuro-psychiatric Symptoms in Alzheimer's Disease.

Materials

Salimetrics Children Swab (SCS) Salimetrics 5001.06 store at RT 50/pack
Swab storage tube (2 ml) Sarstedt 51.1534.004 100/pack
Barcode lables CISBR n/a contact CISBR to order
Color coded polypropylene vial caps (for SST) Sarstedt (see below)
White Sarstedt 65.793.517 1,000/pack
Blue Sarstedt 65.793.513 1,000/pack
Yellow Sarstedt 65.793.514 1,000/pack
Green Sarstedt 65.793.515 1,000/pack
Orange Sarstedt 65.793.516 1,000/pack
Red Sarstedt 65.793.518 1,000/pack
Black Sarstedt 65.793.519 1,000/pack
Violet Sarstedt 65.793.520 1,000/pack
Mixed Colors Sarstedt 65.793.999 1,000/pack
Salivary Cortisol Enzyme Immuno Assay Kit Salimetrics 1.3102 Diagnostic Kit
Salivary Alpha Amylase Enzyme Immuno Assay Kit Salimetrics 1.1902
Nitrile gloves VWR (see below)
X-Small VWR 82026-423 100/box
Small VWR 82026-424 100/box
Medium VWR 82026-426 100/box
Large VWR 82026-428 100/box
X-Large VWR 82026-43 100/box
Insulated Shipping Container ThermoFisher Varies based on size Visit VWR to select size and order
4 in Sample Storage Box (7 x 7) Sarstedt 95.064.949 1 box holds 49 SSTs

References

  1. Granger, D. A., Fortunato, C. F., Beltzer, E. K., Virag, M., Bright, M. A., Out, D. Focus on methodology: Salivary bioscience and research on adolescence: An integrated perspective. Journal of Adolescence. 3 (10), 1081-1095 (2012).
  2. Savla, J. T., Granger, D. A., Roberto, K. A., Davey, A., Blieszner, R., Gwazdauskas, F. Cortisol and alpha amylase reactivity to care-related stressors in spouses of persons with mild cognitive impairment. Psychology and Aging. , (2013).
  3. Hodgson, N. A., Freedman, V., Granger, D., Erno, A. Biobehavioral correlates of relocation in the frail elderly: salivary cortisol, affect, and cognition. Journal of the American Geriatrics Society. 52 (11), 1856-1862 (2004).
  4. Woods, D. L., Kim, H., Yefimova, M. Morning cortisol in relation to behavioral symptoms of nursing home residents with dementia. Biological Reseach in Nursing. (2), 13-132 (2011).
  5. Granger, D. A., Johnson, S. B., Gellman, M. D., Turner, J. R. Salivary Biomarkers. Encyclopedia of Behavioral Medicine. , 1005-1009 (2012).
  6. Nater, U. M., Rohleder, N., Schlotz, W., Ehlert, U., Kirschbaum, C. Determinants of the diurnal course of salivary alpha-amylase). Psychoneuroendocrinology. 32, 392-401 (2007).
  7. Navazech, M. Methods for collecting saliva. Annals of the NY Academy of Sciences. 694, 72-77 (1993).
  8. Dickerson, S. S., Kemeny, M. E. Acute stressors and cortisol responses: A theoretical integration and synthesis of laboratory research. Psychology Bulletin. 130, 355-291 (2004).
  9. Scannapieco, F. A., Papandonatos, G. D., Dunford, R. G. Associations between oral conditions and respiratory disease in a national sample survey population. Annals of Periodontology. 3, 251-256 (1998).
  10. Reibel, J. Tobacco and oral diseases. Update on the evidence, with recommendations. Medical Principles and Practice. 1, 22-32 (2003).
  11. Kivlighan, K. T., Granger, D. A., Schwartz, E. B., Nelson, V., Curran, M., Shirtcliff, E. A. Quantifying blood leakage into the oral mucosa and its effects on the measurement of cortisol, dehydroepiandrosterone, and testosterone in saliva. Hormones and Behavior. 46, 39-46 (2004).
  12. Granger, D. A., Hibel, L. C., Fortunato, C. K., Kapelewski, C. H. Medication effects on salivary cortisol: Tactics and strategy to minimize impact in behavioral and developmental science. Psychoneuroendocrinology. 34, 1437-1448 (2009).
  13. Nater, U. M., Rohleder, N. Salivary alpha-amylase as a noninvasive biomarker for the sympathetic nervous system: Current state of research. Psychoneuroendocrinology. 34 (4), 486-496 (2009).
  14. Hellhammer, J., Fries, E., Schweisthal, O. W., Scholtz, W., Stone, A. A., Hagemann, D. Several measurements are necessary to reliably assess the cortisol rise after awakening: State- and trait-components. Psychoneuroendocrinology. 32, 80-86 (2007).
  15. Pruessner, J., Kirschbaum, C., Meinlschmid, G., Hellhammer, D. H. Two formulas for computation of the area under the curve represent measures of total hormone concentration versus time-dependent change. Psychoneuroendocrinology. 28, 916-931 (2003).
  16. Twisk, J. W. R. . Applied multilevel analysis: A practical guide. , (2006).
  17. Hox, J. J. . Multilevel analysis: Techniques and applications. , (2002).
  18. Adam, E. K., Hoyt, L. T., Granger, D. A. Diurnal alpha-amylase patterns in adolescents: associations with puberty and momentary mood states. Biological Psychology. 88, 170-173 (2011).
  19. Dorn, L. D., Lucke, J. F., Loucks, T. L., Berga, S. L. Salivary cortisol reflects serum cortisol: analysis of circadian profiles. Annals in Clinical Biochemistry. 44, 281-284 (2007).
  20. Donzella, B., Talge, N. M., Smith, T. L., Gunnar, M. R. To spear or not to spear: Comparison of saliva collection methods. Developmental Psychobiology. 50 (7), 714-717 (2007).
  21. Beltzer, E. K., et al. Salivary flow and alpha-amylase: Collection technique, duration, and oral fluid type. Physiology and Behavior. 101 (2), 289-296 (2010).
  22. Granger, D. A., Johnson, S. B., Szanton, S. L., Out, D., Schumann, L. L. Incorporating salivary biomarkers into nursing research: an overview and review of best practices. Biological Research in Nursing. 14 (4), 347-356 (2012).
  23. Shultheiss, O. C., Stanton, S. J., Harmon-Jones, E., Beer, J. S. . Assessment of salivary hormones. Methods in Social Neuroscience. , 17-44 (2009).
check_url/kr/50815?article_type=t

Play Video

Cite This Article
Hodgson, N. A., Granger, D. A. Collecting Saliva and Measuring Salivary Cortisol and Alpha-amylase in Frail Community Residing Older Adults via Family Caregivers. J. Vis. Exp. (82), e50815, doi:10.3791/50815 (2013).

View Video