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Evolution of the Objective Sleep Parameters in Healthy Adult Population

First created | 11/04/2004

Last edited   | 05/11/2012

Written by Maurice M. Ohayon, MD, DSc, PhD

Reference to cite: 1) Ohayon MM. Evolution of the Objective Sleep Parameters in Healthy Adult Population . SleepEval.com Website. Oct 2011. 2) Ohayon MM, Carskadon MA, Guilleminault C, Vitiello MV. Meta-analysis of quantitative sleep parameters from childhood to old age in healthy individuals: developing normative sleep values across the human lifespan. Sleep. 2004 Nov 1;27(7):1255-73. Free PMC


Sleep patterns evolve across the normal aging process in complex ways. Changes in sleep patterns across childhood and adolescence, for example, are not only related to chronological age but also to maturational stage.

 

Few studies, however, have made comprehensive analyses of these two aspects in adolescents (1). Similarly, chronological age in elderly people does not always match physiological age. Therefore, changes in sleep patterns may happen earlier, i.e., at a younger age, for some individuals or at an older age for others. Further, epidemiological and other studies suggest that much of the sleep disturbance typically seen in old age is likely the result of medical co-morbidities than age per se (2-6).

Nevertheless, four age-related changes have been consistently demonstrated in polysomnographic (PSG) studies of sleep architecture: total sleep time (7-29), sleep efficiency (7,9-14,17-23,25-29,30-36), and slow wave sleep (7,8,10, 12-18, 21-28, 31,33, 35,37-39) all decrease, while wake after sleep onset (12-14,16,17,19,21,23,28,29, 32,33,36,37,40) increases with age.

However, a number of PSG sleep characteristics remain uncertain as regard their evolution with age:

(a) sleep latency has been reported to increase with age in some studies (10,13,26,31,40), while several other studies found no significant changes with age (8,9,12, 14,16,17,20-23,28,29,32,33,35-37,39,41). Likewise, a number of studies found no significant differences with age for (b) percentage of stage 1 (9,25,26,35,39,42) and

(c) stage 2 (9,13,20,22,23,25,33,35,36,42,43) while many others reported an increase with age of these stages (7,8,12,17,27,28,31).

(d) Similarly, REM sleep has reported to decrease with age in several studies (7,8,10-12,14,16-18,20,21,23-26,28,31,33,37,38,44) while many other studies found no such association with age (9,13,15,19,22,27,34-36,39-43).

 

Why such discrepancies between the studies?

Several factors may be responsible for the difficulties identifying age trends in sleep architecture of apparently healthy subjects, for example: small sample sizes; inconsistency in controlling factors that may influence sleep, such as mental or physical illness; uncontrolled use of alcohol, drugs or medications; or insufficient screening for sleep disorders.

 

 

methods

 

Targeted studies:

• Non-clinical studies

• “Healthy” participants aged 18 to 60 years

• Included measures of sleep characteristics by “all night” polysomography (PSG)

• Included data presented numerically

• Published between 1960 and 2003 in peer-reviewed journals

 

 

Variables analyzed:

• Sleep latency (SL)

• Sleep efficiency (SE)

• Total sleep time (TST)

• Stage 1, stage 2, slow wave sleep (SWS), REM

 

 

N of studies: 39

N of subjects: 1,450

Age range: 18-60 years

Data examined: TST, SL, SE, REM, S1, S2, SWS

 

“Healthy” participants screened for:

• Physical illnesses (31 studies)

• Sleep apnea (14 studies),

• Sleep disorders (26 studies)

• Mental disorders (27 studies)

• Drug/alcohol use (25 studies)

  

total sleep time

 

 

In studies that screened for physical illnesses, sleep and mental disorders, total sleep time did not change with age.

 

Studies without screening for sleep disorders (d= -0.47) or without screening for mental disorders
(d= -0.24) had significant decrease in TST.

 

Sleep latency

 



Sleep latency increases of only about 5 minutes between 20 and 60 years

 

Inclusion of subjects with sleep or mental disorders had little effect on the effect size; i.e. it does not have an important effect on the association sleep latency and age

 

sleep efficiency

 


In studies that screened for physical illnesses, sleep and mental disorders, sleep efficiency remained unchanged from 20 to 60 years

 

Studies without screening for sleep disorders (d= -0.35) or without screening for mental disorders
(d= -0.34) had significant decrease in sleep efficiency

 

percentage of stage 1

 

In studies that screened for physical illnesses, sleep and mental disorders, percentage of stage 1 sleep significantly increased with age (d=0.48)

 

Inclusion of subjects with sleep (d=0.23) or mental (d=0.30) disorders decreased this association

 

percentage of stage 2

 

 

In studies that screened for physical illnesses, sleep and mental disorders, percentage of stage 2 sleep significantly increased with age (d=0.44)

 

Inclusion of subjects with sleep (d=0.11) or mental (d=0.15) disorders removed this association

percentage Slow Wave Sleep (SWS)

 

 

In studies that screened for physical illnesses, sleep and mental disorders, percentage SWS significantly decreased with age (d=-0.97)

 

Inclusion of subjects with sleep (d=-0.55) or mental (d=-0.67) disorders reduced this association

 

percentage of REM sleep

 

 

In studies that screened for physical illnesses, sleep and mental disorders, percentage of REM sleep significantly decreased with age (d=-0.58).

 

Inclusion of subjects with sleep (d=-0.22) or mental (d=-0.36) disorders reduced this association

 

 

conclusions

 

In healthy adult individuals:

• Total sleep time, sleep latency and sleep efficiency have little variation with age

• Percentage of Stages 1 and 2 increase with age

• SWS and REM decrease

 

Studies that aim to document normal sleep data must carefully exclude participants with physical illnesses, drugs or alcohol use, sleep and mental disorders

 

Studies failing to meet this prerequisite should not be used as reference for normal sleep parameters

 

Procedures, figures, tables, references and analyses of effect sizes are included in the reference paper:
Ohayon MM, Carskadon MA, Guilleminault C, Vitiello MV., Meta-analysis of quantitative sleep parameters from childhood to old age in healthy individuals: developing normative sleep values across the human lifespan. Sleep. 2004 Nov 1;27(7):1255-73. Free PMC



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