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Has Adult Sleep Duration Declined Over the Last 50+ Years?
Summary
The common assumption that population sleep duration has declined in the past few decades has not been supported by recent reviews, which have been limited to self-reported data. The aim of this review was to assess whether there has been a reduction in objectively recorded sleep duration over the last 50+ years.
The literature was searched for studies published from 1960–2013, which assessed objective sleep duration (TST) in healthy normal-sleeping adults. The search found 168 studies that met inclusion criteria, with 257 data points representing 6,052 individuals ages 18–88 years. Data were assessed by comparing the regression lines of age vs. TST in studies conducted between 1960–1989 vs. 1990–2013. Weighted regression analyses assessed the association of year of study with age-adjusted TST across all data points. Regression analyses also assessed the association of year of study with TST separately for 10-year age categories (e.g., ages 18–27 years), and separately for polysomnographic and actigraphic data, and for studies involving a fixed sleep schedule and participants’ customary sleep schedules.
Analyses revealed no significant association of sleep duration with study year. The results are consistent with recent reviews of subjective data, which have challenged the notion of a modern epidemic of insufficient sleep.
Introduction
It has been widely stated that modern industrialized societies have become sleep-deprived. Some studies have suggested that average sleep duration has declined over the last few decades [1–4]. Such findings, combined with extensive epidemiologic evidence associating short sleep with health risks [5–7] and experimental evidence of adverse effects of sleep deprivation [8–10], have provoked widespread concern that chronic insufficient sleep has become a public health crisis.
However, recent reviews of self-reported data have cast doubt on whether nighttime sleep or 24-h sleep has decreased in recent decades, and whether there has been an increased prevalence of short sleep (<6 h), for which risks have been most clearly established. For example, a review of eight studies by Knutson et al. found no significant 31-year trend (1975–2006) towards a higher prevalence of self-reported nighttime sleep of ≤ 6 h [11]. Bin et al. reviewed 12 studies from 15 countries assessed from the 1960s–2000s, and found that sleep duration had increased in 7 countries, decreased in 6 countries, and had not clearly changed in 2 countries [12]. In a subsequent meta-analysis of 38 studies conducted in 10 countries in the 1970s–2000s, Bin et al. [13] found that average 24-h sleep duration had increased in most countries (including the US), and that the prevalence of sleeping ≤ 6 h had decreased in most countries (including the US). Rowshan Ravan et al. studied 36-year trends (1968–2004) in sleep duration among Swedish women, and found no change in 50-year old women, and a decline of only 15 minutes in 38-year old women [14]. Moreover, Bonke reviewed five representative time-use studies spanning 1964–2009, and concluded that “the same number of hours is slept today as in the mid-1960s, with nearly the same prevalence of short and long sleepers” [15].
Discrepancies between studies of population temporal trends in sleep duration can be attributed to multiple factors, including characteristics and representativeness of the respondents, wording of the questions, and instructions given to respondents [16, 17]. Perhaps the biggest limitation of this literature is that it has been limited to self-reports of sleep duration (some of which were retrospective), which can be inaccurate [18, 19] due in part to response biases. The aim of this review was to examine whether there has been a decline over the past 5 decades in sleep duration, as indexed by objective data.
Methods
The search of the literature was modeled after a previous meta-analysis by Ohayon et al., which assessed objective sleep patterns across age [20]. PubMed, PsychLit, selected journals, and reference lists of located manuscripts were searched for studies published between 1960–2013 which met the following criteria: 1) inclusion of presumably healthy adults (as described by the authors), participant ages ≥18 y without sleep problems; 2) report of all-night average total sleep time (TST) measured by polysomnography (PSG) or actigraphy; 3) assessment of sleep under minimally-disturbed conditions, including baseline or placebo conditions, and not involving particularly invasive procedures (e.g., catheterization). Many of the studies included a control group of presumably normal sleepers who had been compared with participants with sleep disorders. Studies involving individuals with extremely high levels of physical fitness were excluded under the assumption that sleep of such individuals might not be representative of the population. Key search words were sleep with normal, normative, healthy, controls, and adults.
The literature searches were performed by two of the authors: either EEG or NK. Questions regarding whether a study met inclusion criteria were resolved in discussions between EEG and SDY or AMR and SDY. Data from the studies were extracted by EEG and AMR.
The search identified >3,500 studies, of which 168 met the inclusion criteria, generating 257 data points across 6,052 individuals. Studies were separated into PSG (Table 1) and actigraphic studies (Table 2). Citations for all included studies are listed in the reference list (#55–222). Coding for each study included the mean sample age (or mid-point of the age range if the mean age was not available), number of men and women subjects, mean sample total sleep time (min), and estimated year of study. Studies with multiple age groups generated multiple data points for the analyses. When available, separate data points for men and women were used. Since most of the studies recorded sleep in the laboratory, only the laboratory data were used for studies that included both home and laboratory data, except for separate analysis of the actigraphy data.
Table 1
Polysomnography studies reviewed for the present paper.
| Polysomnography Studies | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Fixed Sleep Schedule | |||||||||
| Authors | Year Published | Estimated Year of Study | Sample Size | Sample Age Years | Gender | Total Sleep Time (± SD) min | Time in Bed (± SD) min | Excluded First Night | Comments |
| Ryback, Lewis | 1971 | 1970 | n= 8 | 18–24 | not stated | 404.5 | 480 | Yes | Baseline data only |
| Brezinova | 1975 | 1974 | n=24 | 42–66 | M-5 F-9 | 484 ± 22 | 540 | Yes | |
| 20–30 | M-6 F-4 | 455 ± 31 | |||||||
| Nicholson, Stone | 1980 | 1978 | n=6 | 24 | not stated | 443.3 | 480 | Not Stated | Placebo data only |
| Okuma et al. | 1982 | 1982 | n= 8 | 21.1 | M-8 | 444.4 | 480 | Not Stated | Baseline data only |
| Bixler et al. | 1984 | 1984 | n=100 | 19–29 | M-10 F-11 | 440.4 | 480 | Yes | |
| 30–49 | M-16 F-21 | 432.4 | |||||||
| 50–80 | M-14 F-28 | 406.6 | |||||||
| Carskadon, Dement | 1985 | 1985 | n= 10 | 69.3 | M-2 F-8 | 467 ± 54 | 600 | Yes | Baseline data only |
| Roehrs et al. | 1986 | 1986 | n= 12 | 28 | M-12 | 433.2 | 480 | Yes | Placebo group only |
| Libert et al. | 1988 | 1988 | n= 6 | 20–29 | M-6 | 444.4 ±19.7 | 480 | Yes | Baseline data only |
| Gillberg, Akerstedt | 1994 | 1993 | n= 7 | 19–21 | No Data | 456 ±6.4 | 480 | Yes | 8-hour treatment data only |
| Walsh et al. | 1994 | 1993 | n= 12 | 23.5 | M-9 F-3 | 465 | 510 | Not Stated | ND (no sleep disruption condition) night two data only |
| Carrier, Dumont | 1995 | 1995 | n= 23 | 22.8 | M-18 F-5 | 463.68 | 480 | Not Stated | Baseline data only |
| Landolt et al. | 1995 | 1995 | n= 9 | 22.4 | M-9 | 452.67 | 480 | Yes | Placebo, baseline night data only |
| Mann et al. | 1996 | 1995 | n= 11 | 24.8 | M-11 | 393.5 ±19 | 480 | Yes | Baseline data only |
| Landolt et al. | 1996 | 1994 | n= 10 | 61.6 | M-10 | 413.4 | 480 | Yes | Baseline data only |
| Landolt et al. | 1996 | 1995 | n=16 | 20–26 | M-8 | 449.7 ±4.7 | 480 | Yes | |
| 57–64 | M-8 | 409.2 ±7.9 | 480 | ||||||
| Cajochen et al. | 1997 | 1995 | n= 8 | 23–32 | M-8 | 443.6 ±10.6 | 480 | Yes | Placebo, pretreatment night data only |
| Martin et al. | 1997 | 1996 | n= 12 | 25 | M-7 | 419.0 ±27.4 | 450 | Yes | Disregarding data from fragmented sleep night |
| Rao et al | 1998 | 1998 | n= 17 | African American 30.9 | M-6 F-11 | 416.9 ±45.7 | 480 | Not Stated | |
| n= 10 | Asian 28.4 | M-6 F-4 | 404.3 ±29.2 | 480 | |||||
| n= 30 | Caucasian 42.2 | M-16 F-14 | 406.4 ±52.5 | 480 | |||||
| n= 16 | Hispanic 27.7 | M-7 F-9 | 440.6 | 480 | |||||
| Harma et al. | 1998 | 1996 | n= 2 | 28.9 | F-2 | 421 ± 24 | 480 | Yes | Controls only |
| Yassouridis et al. | 1999 | 1997 | n= 30 | 27.5 | M-30 | 432.21 ±16.5 | 480 | Yes | |
| Sharkey et al. | 2001 | 2000 | n= 21 | 27 | M-12 F-9 | 459 ± 12 | 480 | Yes | Baseline, placebo data only |
| Onen et al. | 2001 | 2000 | n= 9 | 31 | M-9 | 426.3 ±11.7 | 480 | Yes | Baseline data only |
| Gaudreau et al. | 2001 | 1999 | n=54 | 19–29 | M-10 F-5 | 502.53 ±46.32 | 570 | Yes | > 18 year old data plotted only |
| 36–60 | M-10 F-5 | 439.49 ±34.54 | 480 | ||||||
| Huber et al. | 2002 | 2002 | n= 16 | 22.3 | M-16 | 446.4 ±3 | 480 | Yes | Sham data only |
| Mukai et al. | 2003 | 2001 | n= 8 | 24.5 | M-8 | 456.3 ±15.7 | 480 | Yes | Normal sleepers only |
| Brandenberger et al. | 2003 | 2002 | n= 24 | 21.1 | M-10 F-2 | 449.2 ±4 | 480 | Yes | |
| 64.9 | M-10 F-2 | 409.5 ±85 | |||||||
| Waters et al. | 2003 | 2002 | n= 77 | 26.5 | M-77 | 406.8 | 480 | Yes | Placebo data only |
| LaJambe et al. | 2005 | 2004 | n= 8 | 18–35 | no data per group | 389.6 ±24 | 480 | Yes | Placebo data only |
| Drapeau et al. | 2006 | 2005 | n= 12 | 23.8 | M-6 F-6 | 460 ± 12 | 480 | Yes | Placebo data only |
| n= 12 | 50.3 | M-5 F-7 | 395 ± 15 | ||||||
| Hornyak et al. | 2007 | 2006 | n= 35 | 19–69 | M-16 F-29 | 425.4 ±34.3 | 480 ±30 | Yes | Controls only |
| Wong et al. | 2008 | 2007 | n= 9 | 27.8 | M-9 F-1 | 390 | 480 | Yes | Control data only |
| Schmid et al. | 2008 | 2007 | n= 9 | 24.2 | M-9 | 418 ± 11 | 420 | Not Stated | Seven hour TIB data only |
| Cote et al. | 2009 | 2008 | n= 12 | 21 | M-4 F-13 | 450 | 480 | Yes | Baseline data only |
| Bixler et al. | 2009 | 2007 | n= 66 | 23.5 | M-32 | 432 | 480 | Yes | Baseline data only |
| 24.2 | F-34 | 430 | 480 | ||||||
| Vandekerckhove et al. | 2011 | 2010 | n= 13 | 19–56 | M-6 F-7 | 457.42 ±32.65 | 480 | Yes | Baseline (first data point) neutral data (second data point) |
| 445.46 ±45.77 | |||||||||
| Brower et al. | 2011 | 2010 | n= 10 | 20–40 | no data | 389.3 ±10.3 | 420 | Yes | Baseline data only for healthy control |
| Schmid et al. | 2012 | 2011 | n= 23 | 23.2 | M-23 | 462.1 ±1.3 | 480 | Yes | Sham data only |
| Schmid et al. | 2012 | 2011 | n= 30 | 23 | M-30 | 456.5 ±2.4 | 480 | Screening night included | Sham data only |
| Flausino et al. | 2012 | 2011 | n= 18 | 27.2 | M-18 | 339.1 ±54.9 | 480 | Not Stated | Baseline data only. Data deleted as outlier |
| Holz et al. | 2012 | 2012 | n= 20 | 27.1 | M-10 F-10 | 418.7 | 480 | Yes | Baseline data only |
| Rosipal et al. | 2013 | 2012 | n=148 | 20–86 | M-67 F-81 | 384 | 474 | Yes | Data from two nights; used only 2nd night |
| 408 | 474 | ||||||||
| Tonetti et al. | 2013 | 2012 | n= 11 | 24.75 | M-4 F-7 | 401.18 ±47.96 | 480 | Not Stated | PSG data only, WS device data not included |
| Normal Sleep Schedule | |||||||||
| Feinberg et al. | 1967 | 1966 | n=30 | 19–36 | M-9 F-6 | 393.9 ±28.1 | 420.7 ±2.0 | Yes | Healthy control data only |
| 65–96 | M-9 F-6 | 384.4 ±36.5 | 468.9 ±38.3 | ||||||
| Walker et al. | 1977 | 1975 | n= 10 | 18–22 | M-10 | 441.0 ±27.5 | 478.6 ±3 | Yes | Nonrunner, baseline data only |
| Gaillard | 1978 | 1977 | n= 40 | 19–21 | n=12 | 504 ± 36 | 529 ± 38 | Yes | |
| 22–24 | n=11 | 505 ± 45 | 525 ±38 | ||||||
| 25–27 | n=11 | 491 ±49 | 517 ± 43 | ||||||
| 28–30 | n=6 | 460 ± 49 | 507 ± 40 | ||||||
| Browman | 1980 | 1979 | n= 8 | 19–22 | M-8 | 407.3 ±43.1 | 418.57 ±50.89 | Yes | Baseline data only |
| Adam | 1980 | 1979 | n= 16 | 59 | M-6 F-10 | 455.1±24.8 | Normal Sleep Patterns | Yes | Placebo capsule data |
| Philipson et al. | 1980 | 1978 | n= 46 | 24 | M-37 F-9 | 439.3 | 481.3 | Yes | |
| Coates et al. | 1981 | 1981 | n= 12 | 23–60 | M-6 F-6 | 388 ±55.4 | Normal Sleep Patterns | Yes | Night two data only |
| Montgomery et al. | 1982 | 1982 | n= 12 | 23.3 | M-4 F-4 | 428. 4 | 455.3 | Yes | Unfit subjects, however still fit healthy criteria |
| Trinder et al. | 1982 | 1982 | n= 6 | 22.3 | not stated | 401.4 | 452.3 | Yes | Unfit subjects, however still fit healthy criteria |
| n= 6 | 31.8 | not stated | 420.2 | 449.4 | |||||
| Paxton et al. | 1983 | 1983 | n= 9 | 20.67 | M-9 | 416 | 446 | Yes | Normal, unfit data only. Used average of 2 nights |
| 426 | 454 | ||||||||
| Bunnell et al. | 1983 | 1983 | n= 9 | 25 | M-4 F-5 | 436.2 ± 11.1 | Normal Sleep Patterns | Not Stated | Baseline data only |
| Horne, Staff | 1983 | 1983 | n= 8 | 25.4 | M-8 | 464.5 ± 20.5 | Normal Sleep Patterns | Yes | Baseline data only |
| Matsumoto et al. | 1984 | 1984 | n= 6 | 20–24 | M-6 | 389.0 ± 11.5 | Normal Sleep Patterns | Not Stated | No exercise group |
| Paxton et al. | 1984 | 1984 | n= 17 | 20 | M-17 | 449 ± 49.5 | 489 ± 25.2 | Yes | Non-athlete. Baseline data only |
| Reynolds et al. | 1985 | 1985 | n= 24 | 69.5 | M-8 F-16 | 367.4 ± 45 | Normal Sleep Patterns | Yes | Healthy control data only |
| Bonnet | 1985 | 1985 | n= 11 | 18–32 | not stated | 389 | Normal Sleep Patterns | Yes | Baseline data only |
| Kupfer et al. | 1985 | 1985 | n= 10 | 24.8 | M-10 | 396.6 ± 47.6 | Normal Sleep Patterns | Yes | No exercise group |
| Nakagawa | 1987 | 1987 | n= 6 | 19– 23 | M-6 | 501.8 ± 28.2 | 523.0 ± 30.7 | Yes | Baseline data only |
| Naifeh et al. | 1987 | 1987 | n=23 | 30–40 | M-6 F-6 | 386 ± 40 | 404 ± 46 | Not Stated | |
| 60 + | M-5 F-6 | 364 ± 47 | 422 ± 58 | ||||||
| Hudson et al. | 1988 | 1988 | n=18 | 20–55 | M-8 F-10 | 384.9 ± 30.7 | 421.1 ± 27.5 | Yes | Controls only |
| Schiavi, Schreiner-Engel | 1988 | 1988 | n=40 | 23–29 | M-11 | 404 ± 36 | 441 ± 36 | Yes | |
| 30–39 | M-5 | 411 ± 34 | 448 ± 41 | ||||||
| 40–49 | M-8 | 387 ± 42 | 434 ± 26 | ||||||
| 50–59 | M-7 | 332 ± 51 | 398 ± 39 | ||||||
| 60–73 | M-9 | 317 ± 53 | 397 ± 39 | ||||||
| Hoch et al. | 1988 | 1988 | n=19 | 60–82 | M-9 F-10 | 350.1 ± 64.9 | 467.3 | Yes | |
| 370.9± 29.6 | 455.8 | ||||||||
| Mellman, Uhde | 1989 | 1989 | n=7 | 26–49 | M-5 F-2 | 439.6 ± 45.3 | Normal Sleep Patterns | Yes | Controls only |
| Bonnet | 1989 | 1989 | n=24 | 22 | M-12 | 372 | 411 | Yes | |
| 63 | M-12 | 363 | 430 | ||||||
| Lydiard et al | 1989 | 1989 | n=14 | 30.1 | No Data | 384.9 ± 31.4 | Normal Sleep Patterns | Yes | Controls only |
| Saletu et al | 1990 | 1990 | n=16 | 23–39 | M-8 F-8 | 385.66 ± 78.55 | 426.65 ± 19.4 | Yes | Baseline data only |
| Vitiello et al. | 1990 | 1990 | n= 24 | 63.6 | M-11 F-13 | 385.1 | 456.5 | Yes | Controls only |
| Brendel et al | 1990 | 1990 | n=10 | 83 | M-6 F-4 | 395.5 ± 70.1 | 491.5 ± 55.7 | Yes | Nights two and three |
| n=14 | 23.9 | M-10 F-4 | 429.8 ± 31.4 | 445.0 ± 42.4 | |||||
| Hoch et al | 1990 | 1990 | n=34 | 60–69 | M-21 F-13 | 335.1 ± 62.3 | 430.6 | Yes | |
| n=33 | 70–79 | M-17 F-16 | 328.5 ± 56.4 | 431.9 | |||||
| n=38 | 80–89 | M-19 F-19 | 318.1 ± 81.4 | 437.3 | |||||
| Lauer et al. | 1991 | 1991 | n=13 | 18–24 | M-26 F-25 total Not specified for age groups | 413.9 ± 16 | 422.3 | Not Stated | Controls only |
| n= 10 | 25–34 | 417.6 ± 23.6 | 428.8 | ||||||
| n= 10 | 35–44 | 404.6 ± 34.2 | 424.1 | ||||||
| n= 9 | 45–54 | 363.1 ± 44.5 | 397.2 | ||||||
| n= 9 | 55–65 | 350.0 ± 36.3 | 385.8 | ||||||
| Monk et al. | 1991 | 1991 | n=34 | 80–91 | M-16 F-18 | 368 ± 50 | 478 | Yes | |
| n=30 | 21–30 | M-21 F-9 | 426 ± 39 | 507 | |||||
| Van Coevorden et al. | 1991 | 1990 | n= 8 | 20–27 | M-8 | 479 ± 48 | Normal sleep Patterns | Yes | Non-catheter data only |
| n= 8 | 67–84 | M-8 | 454 ± 53 | ||||||
| Wauquier et al. | 1992 | 1992 | n= 7 | 88–102 | F-7 | 438 ± 27.6 | 566 ± 22.8 | Yes | |
| n= 7 | 88–98 | F-7 | 328 ± 14.1 | 462 ± 14.6 | |||||
| Bonnet, Arand | 1992 | 1992 | n= 12 | 18–30 | M-12 | 445 | 472 | Yes | Baseline data only |
| Hudson et al | 1992 | 1992 | n= 19 | 24.5 | M-7 F-12 | 407 ± 35 | 437 ± 32 | Yes | Controls only |
| Monk et al. | 1992 | 1992 | n= 25 | 71–91 | F-25 | 366 ± 37 | Normal Sleep Patterns | Not Stated | |
| n= 20 | 71–97 | M-20 | 338 ± 48 | ||||||
| n= 21 | 19–28 | M-10 F-11 | 415 ± 47 | ||||||
| Buysse et al | 1992 | 1992 | n=45 | > 78 | M-21 F-24 | 365.0 ± 62.0 | Normal Sleep Patterns | Yes | |
| n=33 | 20–30 | M-20 F-13 | 426.5 ± 36.4 | ||||||
| Hirshkowitz et al. | 1992 | 1992 | n=44 | 20–29 | M-44 | 347.3 ± 62.5 | 404.9 ± 44.1 | Yes | |
| n=23 | 30–39 | M-23 | 340.0 ± 70.8 | 393.1 ± 58.2 | |||||
| n=49 | 40–49 | M-49 | 329.4 ± 54.6 | 404.2 ± 49.4 | |||||
| n=41 | 50–59 | M-41 | 331.6 ± 63.6 | 393.0 ± 51.1 | |||||
| n=29 | >60 | M-29 | 298.4 ± 61.3 | 395.7 ± 42.8 | |||||
| Montmayeur, Buguet | 1992 | 1992 | n= 6 | 36 | M-6 | 357.8 ± 16.2 | Normal Sleep Patterns | Not Stated | Data from intermediate temperature only (March) |
| Dijk, Czeisler | 1993 | 1993 | n= 9 | 21–30 | M-9 | 431.8 ± 6.3 | Normal Sleep Patterns | Yes | Baseline data only |
| Hoch et al. | 1994 | 1994 | n=27 | <75 | M-21 F-29 | 378.6 ± 40.5 | Normal Sleep Patterns | Yes | Baseline data |
| n=23 | ≥75 | 363.9 ± 57.4 | |||||||
| Buguet et al. | 1995 | 1994 | n= 6 | 24 | No data | 441.2 ± 4.9 | 489.1 ± 2.3 | Not Stated | Placebo, baseline night data only |
| Hajak et al. | 1996 | 1995 | n= 10 | 25.6 | M-5 | 419.1 ± 62.1 | 483 ± 16 | Yes | Placebo data only |
| 49.4 | M-5 | 389 ± 44.6 | 455 ± 20 min | ||||||
| Carrier et al. | 1996 | 1995 | n= 24 | 82.2 | M-10 F-14 | 370.3 ± 7.9 | 460 | Yes | Baseline data only |
| Vitiello et al. | 1996 | 1995 | n= 68 | 55–80+ | F-68 | 393.2 ± 6 | 465.8 ± 5.9 | Yes | Non-catheter data only |
| n= 45 | 60–80+ | M-45 | 369.8 ± 7.3 | 445.3 ± 8.5 | |||||
| Ehlers, Kupfer | 1997 | 1996 | n=61 | 20–29 | M-18 | 447.83 | 477.58 | Yes | |
| F-14 | 457.71 | 483.43 | |||||||
| 30–40 | M-15 | 413 | 445.57 | ||||||
| F-14 | 415.5 | 439.4 | |||||||
| Haimov, Lavie | 1997 | 1996 | n=17 | 65–75 | M-17 | 330.2 ± 33.4 | Normal Sleep Patterns | Yes | |
| n=8 | 19–26 | M-8 | 354.3 ± 38.4 | ||||||
| Carrier et al. | 1997 | 1997 | n= 39 | 29.99 | M-52 F-58 | 457.73 ± 44.36 | 460.6 ± 4.3 | Yes | |
| n= 37 | 34.79 | 423.05 ± 36.4 | |||||||
| n= 33 | 47.64 | 405.96 ± 37.52 | |||||||
| Edinger et al. | 1997 | 1997 | n=32 | 67.5 | M-16 F-16 | 363.6 (Home) | Normal Sleep Patterns | No | Used only night 2 in the lab |
| 347.5 (Home) | |||||||||
| 371.8 (Lab) | |||||||||
| 361.1 (Lab) | |||||||||
| Cajochen et al. | 1998 | 1997 | n= 10 | 27 | M-10 | 423.5 ± 5 | Normal Sleep Patterns | Yes | Placebo, treatment night data only |
| Lushington et al. | 1999 | 1997 | n= 16 | 65.4 | M-5 F-11 | 449.3 ± 8 | 530 ± 6 | Yes | |
| Armitage et al. | 2000 | 1999 | n=23 | 22–40 | M-15 | 384.5 | Normal Sleep Patterns | Yes | Controls only |
| F-8 | 410.3 | ||||||||
| Carrier et al. | 2001 | 1999 | n=100 | 20–39 | M-31 F-27 | 428.9 | Normal Sleep Patterns | Yes | |
| 40–60 | M-22 F-20 | 404.3 | |||||||
| Nicolas et al. | 2001 | 2000 | n=30 | 20–29 | M-3 F-3 | 433.07 ± 32.99 | Normal Sleep Patterns | Yes | |
| 30–39 | M-3 F-3 | 451.53 ± 47.45 | |||||||
| 40–49 | M-3 F-3 | 431.47 ± 22.09 | |||||||
| 50–59 | M-3 F-3 | 447.65 ± 39.00 | |||||||
| 60–69 | M-2 F-4 | 379.12 ± 41.28 | |||||||
| Edinger et al. | 2001 | 2000 | n= 35 | 40–59 | M-17 F-18 | 377.6 ± 10.5 | Normal Sleep Patterns | Yes | Controls only (Home) |
| Roky et al. | 2001 | 1999 | n= 8 | 20–28 | M-8 | 422 ± 9 | Normal Sleep Patterns | Yes | Baseline data only |
| Means et al. | 2003 | 2002 | n= 49 | 55.4 | M-27 F-22 | 376.9 ± 46.5 (Home) | 452.0 ± 63.3 | Yes | Disregarded insomnia patient data |
| 371.2 ± 41.2 (Lab) | 430.7 ± 45.8 | ||||||||
| Kato et al. | 2004 | 2003 | n= 10 | 24.6 | M-4 F-6 | 452 ± 17 | Normal Sleep Patterns | Yes | Baseline data only |
| Penev | 2007 | 2006 | n=12 | 68.9 | M-12 | 383 ± 58 | 436 | Yes | |
| Carrier et al. | 2007 | 2006 | n= 17 | 37.2 | M-7 F-10 | 426.1 ± 16 | 504 | Not Stated | Placebo data only |
| Peters et al. | 2008 | 2007 | n= 28 | 20.14 | M-7 F-7 | 483.12 ± 35.32 | Normal Sleep Patterns | Yes | Baseline data only |
| 69.79 | M-7 F-7 | 445. 43 ± 71.7 | |||||||
| O'Donnell et al. | 2009 | 2008 | n= 24 | 64 | M-11 F-13 | 377.5 ± 37.6 | Normal Sleep Patterns | Yes | Baseline data only |
| Paterson et al. | 2009 | 2008 | n= 12 | 24.9 | M-12 | 458 ± 12 | Normal Sleep Patterns | Yes | Placebo data only |
| Robillard et al. | 2010 | 2008 | n= 87 | 23.3 | M-26 F-22 | 438 | Normal Sleep Patterns | Not Stated | |
| 51.9 | M-18 F-21 | 404 | |||||||
| Morgan et al. | 2010 | 2008 | n= 12 | 39 | M-12 | 416 ± 15 | Normal Sleep Patterns | Placebo data only | |
| Marzano et al. | 2010 | 2009 | n= 10 | 23.8 | M-10 F-10 | 441.4 ± 38 | 484.8 ± 63 | Yes | Baseline data only |
| Ferri et al. | 2010 | 2009 | n= 15 | 24.6 | M-12 F-3 | 449.6 ± 18.41 | 483.0 ± 16 | Not Stated | |
| Herbst et al | 2010 | 2009 | n= 26 | 39.8 | M-13 F-13 | 386.56 ± 83.95 | Normal Sleep Patterns | Yes | Night one and night two data |
| 395.27 ± 68.49 | |||||||||
| Nissen et al. | 2011 | 2009 | n= 26 | 46.3 | M-14 F-12 | 390.4 | Normal Sleep Patterns | Not Stated | Controls only |
| Hebert et al. | 2011 | 2009 | n= 22 | 60.4 | M-8 F-14 | 376.6 ± 59.6 | Normal Sleep Patterns | No | Controls only |
| Danker-Hopfe et al. | 2011 | 2009 | n= 30 | 25.3 | M-30 | 456.3 ± 16.6 | Normal Sleep Patterns | Yes | Sham data only |
| Marzano et al. | 2011 | 2009 | n= 50 | 24.3 | M-29 F-21 | 443.26 | Normal Sleep Patterns | Yes | Baseline data only |
| Gonzalez et al. | 2011 | 2010 | n= 20 | 28–64 | F-20 | 357.31 ± 41.5 | 420.59 ± 20.74 | Not Stated | Control data only |
| Bianchi et al. | 2012 | 2011 | n= 32 | 18–32 | M-16 F-16 | 474 ± 48 | 516 | Recorded as baseline | Baseline data only |
| n= 12 | 60–76 | M-5 F-7 | 402 ± 48 | 485 | |||||
| Ferri, Bruni et al. | 2012 | 2011 | n= 98 | 29.7 | M-12 F-13 | 393.7 | 438.5 | Not Stated | > 18 year old data only |
| 62.2 | M-4 F-6 | 410.8 | 526.6 | ||||||
| 73.4 | M-3 F-6 | 345.1 | 487.7 | ||||||
| Frey et al. | 2012 | 2011 | n= 8 | 20–31 | F-8 | 446.2 ± 26.9 | Normal Sleep Patterns | Yes | Disregarded depression data, baseline data only. |
| n= 8 | 57–74 | F-8 | 408.5 ± 42.5 | ||||||
| Kobayashi et al. | 2012 | 2011 | n=22 | 22.6 | M-15 F-8 | 373.1 ± 136.2 | Normal Sleep Patterns | Yes | Non-PTSD subjects Only used |
| 408.1 ± 81.7 | |||||||||
| Ferri et al. | 2013 | 2012 | n=18 | 69.4 | M-10 F-8 | 382.5± 53.11 | 517.2 ± 64.31 | Yes | |
| Chellappa et al. | 2013 | 2012 | n= 30 | 25.2 | M-16 F-14 | 390.7 ± 3.1 | Normal Sleep Patterns | Not Stated | Classic light data only |
| Robey et al. | 2013 | 2012 | n= 11 | 26 | M-11 | 410.9 ± 14.3 | 438.9 ± 8 | Yes | Control data only |
| Richards et al. | 2013 | 2012 | n= 43 | 30.39 | M-22 F-21 | 403.66 | Normal Sleep Patterns | Not Stated | Control data only |
| Saxvig et al. | 2013 | 2012 | n= 19 | 21.1 | M-5 F-14 | 507 ± 68.8 | 551 ± 67.2 | Yes | Control data only |
| Sleep Schedule Not Stated | |||||||||
| Kahn et al. | 1970 | 1968 | n=10 | 76.7 | F-10 | 383 ± 46.6 | Not stated | Yes | |
| Williamset al. | 1972 | 1970 | n=10 | 41–46 | M-10 | 376.6 ± 35.7 | Not stated | Yes | |
| Browman, Tepas | 1976 | 1975 | n= 9 | 18.89 | M-9 | 456 | Not stated | Yes | Relaxation data group only |
| Karacan et al. | 1976 | 1975 | n= 18 | 20–30 | M-18 | 416 | Not stated | Yes | Baseline data only |
| Adam | 1982 | 1982 | n= 7 | 58 | M-4 F-3 | 456.5 ± 29.7 | Not stated | Yes | Non-catheter night only |
| Berry, Webb | 1985 | 1985 | n=119 | 50–70 | M-55 | 400.7 | Not stated | Yes | |
| F-64 | 403.8 | ||||||||
| Reynolds et al. | 1986 | 1986 | n= 20 | 70.1 | M-10 | 374 ± 48 | Not stated | Yes | Baseline data only |
| 68.7 | F-10 | 361.8 ± 42.6 | |||||||
| James et al. | 1987 | 1987 | n= 10 | 29.9 | M-7 F-3 | 436.9 ± 32.8 | Not stated | Yes | Placebo group only |
| Stone et al. | 2000 | 1999 | n= 7 | 23.4 | M-7 | 417.0 ± 26.6 | Not stated | Yes | |
| Youngstedt et al. | 2000 | 1998 | n=8 | 24.5 | M-8 | 424.3 ± 14.4 | Not stated | Yes | |
| Crowley et al. | 2002 | 2001 | n=34 | 18–25 | M-8 F-6 | 453.3 ± 92.7 | Not stated | Yes | |
| 74.6 | M-11 | 341.7 ± 65.5 | Not stated | ||||||
| 76.7 | F-9 | ||||||||
| Edinger et al. | 2003 | 2003 | n=34 | 46.5 | M-16 F-18 | 370.5 ± 10.1 (Lab) | Ad Lib | Yes | Normal patient data only |
| 379.6 ± 11.3 (Home) | |||||||||
| De Souza et al. | 2003 | 2001 | n= 21 | 18–33 | M-7 F-14 | 414.8 ± 43.2 | Not stated | Yes | |
| Beaumont et al. | 2004 | 2002 | n= 9 | 35.3 | M-6 F-3 | 395 ± 25 | Not stated | Yes | Placebo data only |
| Mahlberg, Kunz | 2007 | 2006 | n= 29 | 24–86 | M-13 F-16 | 396.8 ± 50.2 | Not stated | Yes | Healthy subject only |
| Bonnet, Arand | 2007 | 2006 | n= 12 | 18–20 | M-3 F-9 | 439 | Not stated | No | Data corrected for arousals associated with limb movements and apnea |
| n= 13 | 21–30 | M-7 F-6 | 446 | ||||||
| n=13 | 31–40 | M-7 F-6 | 403 | ||||||
| n=10 | 41–50 | M-6 F-4 | 395 | ||||||
| n=14 | 51–60 | M-12 F-2 | 358 | ||||||
| n=14 | 61–70 | M-12 F-2 | 350 | ||||||
| Jaehne et al | 2012 | 2011 | n= 44 | 18–52 | M-29 F-15 | 430.5 ± 17.06 | Not stated | Yes | Smoker data disregarded |
Table 2
Actigraphic studies reviewed for the present paper.
| Actigraphic Studies | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Fixed Sleep Schedule | |||||||||
| Authors | Year Published | Estimated Year of Study | Sample Size | Sample Age Years | Gender | Total Sleep Time (± SD) min | Time in Bed (± SD) min | Excluded First Night | Comments |
| Blagrove et al. | 1998 | 1996 | n= 9 | 20 | F-9 | 421 ± 12.2 | 480 | Yes | |
| Hindmarch et al. | 2000 | 1998 | n= 30 | 27.3 | M-15 F-15 | 441.6 | 510 | Yes | Placebo data only |
| Jean-Louis et al. | 2001 | 1999 | n= 11 | 25.36 | M-4 F-7 | 441 | 480 | Yes | |
| Jean-Louis et al. | 2001 | 1999 | n=5 | 25 | no data | 449 ± 19 | 480 | Yes | |
| Baskett et al. | 2003 | 2001 | n= 20 | 71.7 | M-4 F-16 | 443 | 480 | Yes | Baseline data only |
| Yoon et al. | 2003 | 2002 | n=133 | 18–32 | M-26 F-47 | 420.8 ± 48.2 | 474.5 ± 54.5 | Yes | |
| 60–75 | M-22 F-38 | 366.1 ± 53.2 | 475.9 ± 64.3 | ||||||
| O’Hare et al. | 2014 | 2013 | n=20 | 30 | M-11 F-9 | 391 ± 49 | 450 | Not Stated | |
| Normal Sleep Schedule | |||||||||
| Jean-Louis et al. | 1996 | 1996 | n= 20 | 29.95 | M-11 F-9 | 391 ± 57 | Normal Sleep Patterns | Not Stated | Validation night only |
| Hume et al. | 1998 | 1997 | n= 190 | 20–34 | M-39 F-23 | 458 ± 54 | Normal Sleep Patterns | Yes | |
| 35–49 | M-22 F-42 | 422 ±60 | |||||||
| 50–70 | M-26 F-38 | 412 ± 55 | |||||||
| Pires et al. | 2001 | 2000 | n= 6 | 22–24 | M-6 | 558.7 ±73 | Normal Sleep Patterns | Yes | Placebo data only. Data from PSG |
| 511.5 ± 101 | |||||||||
| 517.7 ± 39 | |||||||||
| Youngstedt et al. | 2003 | 2002 | n= 71 | 18–75 | no data | 380.95 ± 5.8 | Not stated | No, because at home | |
| Benson et al. | 2004 | 2003 | n= 20 | 35.35 | M-7 F-13 | 383.93 ±70.29 | Normal Sleep Patterns | No, because at home | |
| Monk et al | 2006 | 2005 | n= 128 | 70–92 | M-65 F-63 | 413 ± 83 | 449 ± 76 | Not Stated | |
| Robertson et al. | 2007 | 2006 | n= 15 | 27.7 | M-7 F-8 | 374 ± 56.8 | Normal Sleep Patterns | Not Stated | Normal sleepers only. |
| Rahman et al. | 2011 | 2010 | n=15 | 35.6 | M-5 F-10 | 486 ±54 | Normal Sleep Patterns | Control data only. | |
| Kogure et al. | 2011 | 2010 | n= 45 | 50.2 | M-16 F-17 | 436 ± 69 | Normal Sleep Patterns | No, because at home | |
| 83.8 | F-12 | 410 ± 72.9 | |||||||
| Myllymäki et al. | 2011 | 2010 | n= 11 | 25 | M-7 F-4 | 437.7 ± 45 | 486 | Yes | Control data only |
| Scatena et al. | 2012 | 2011 | n= 25 | 44.3 | M-13 F-12 | 736.7 ± 121.8 | Normal Sleep Patterns | Not Stated | Data deleted as outlier |
| Robertson et al. | 2013 | 2012 | n= 19 | 20–30 | M-19 | 369 ± 40.5 | Not stated | Not Stated | Baseline data only. |
| Petersen et al. | 2013 | 2012 | n= 28 | 41 | M-7 F-21 | 381.81 ± 11.3 | 491 | Yes | Low sensitivity, low stress data only |
| Sleep Schedule Not Stated | |||||||||
| Naylor et al. | 2000 | 1999 | n= 14 | 75.2 | M-5 F-9 | 337.6 ± 19.5 | Not stated | Yes | Controls only |
| Gooneratne et al. | 2011 | 2009 | n= 100 | 72.5 | M-37 F-63 | 371.1 | Not stated | Yes | > 18 year old data only |
| Wulff et al. | 2012 | 2010 | n= 21 | 37.5 | M-13 F-8 | 364.8 ± 37.2 | Not stated | Not Stated | Control data only. |
| Shambroom et al. | 2012 | 2010 | n=26 | 38 | M-13 F-13 | 324.6 ± 11.2 | Not stated | Yes | |
| Ju et al | 2013 | 2012 | n=142 | 65.6 | M-58 F-84 | 402.6±44.6 | 486.4 ±49.8 | Not Stated | |
| Winser et al. | 2013 | 2012 | n=39 | 26.5 | M-12 | 428 ± 55.2 | Not Stated | Not stated | |
| 27.9 | F-27 | 434.1 ± 40 | |||||||
| Lombardi et al | 2013 | 2012 | n= 23 | 40.6 | M-23 | 420 | Not Stated | Not stated | Sea level data only |
| n= 14 | 36.1 | F-14 | |||||||
Since the year of publication of a study often differed from the year in which a study was conducted, the following rules were used to estimate the year that a study had been conducted. 1) Year of study was estimated by subtracting 10 months from the posted date of journal receipt of the manuscript for studies with <50 subjects, 14 months for studies with 50–99 subjects, 18 months for studies with 100–149 subjects, and 22 months for studies with ≥150 subjects. 2) If information was available regarding the date a paper was accepted, but not the date that it was received, the median across-the-literature duration in months between date received and date accepted (4 months) was subtracted from the date of publication, and Rule 1 was followed. 3) If neither date accepted nor date received information was available, the median number of months between date received and date published (11 months) was subtracted from the date of publication, and Rule 1 was followed.
The TST data were first assessed by comparing the intercepts of the regression lines of age vs. TST for studies conducted between 1960–1989 vs. 1990–2013. We chose this split to obtain a more balanced number of data points across the years split. Another reason for the1989/1990 split was that it has been posited that the obesity epidemic, which started shortly after this time, can be partly attributed to declines in sleep. Examining the intercepts allowed an assessment of temporal differences in TST across all data points (without adjustment for age). A temporal decline in TST would be revealed by a smaller intercept for the 1990–2013 studies compared with the 1960–1989 studies. Another rationale for the1989/1990 split was that it has been posited that the obesity epidemic, which started shortly after this time, can be partly attributed to declines in sleep [21].
To further assess a temporal trend of TST across all data points, a linear regression analysis of year of study (weighted for sample size) and participants’ age vs. TST was calculated. To plot these data, age-adjusted TST was determined based on the slope of the linear regression between TST and age across all data points. An a priori decision was made to remove outlying samples, for which mean age-adjusted TST was ≥ 2 standard deviations from the mean value across the literature. Two data points were removed based on this criterion. Weighted linear regression analyses were also conducted for year of study vs. TST across 10-year age categories (e.g, ages 18–27 years, 28–37 years, etc.).
Separate weighted linear regression analyses were conducted for data from studies in which participants followed their usual sleep schedules and for studies involving a fixed sleep period; for polysomnographic and actigraphic data; and for data involving men only and women only. Plots of year of study vs. age-adjusted TST were performed for each of these analyses.
Results
The intercepts and slopes of the regression lines of age vs. TST did not differ for studies conducted between 1960–1989 and 1990–2013 (Figure 1). In the regression analysis across all data points (n=257), there was no significant association of year of study with TST (b=.03, p=0.56) (Figure 2), nor was there a significant association of study year with TST for any of the 10-year age categories (Figure 3) (p=0.40–0.92). Likewise, there was no significant association of year of study in analyses restricted to PSG (n=225) (b=0.03, p=0.63) or to actigraphic data (n=32) (b=−0.17, p=0.38) (Figure 4); or in analyses involving only men (n=71) or only women (n=17) (Figure 5). Finally, there was no significant association in analyses derived from studies in which subjects followed their usual sleep periods (n=154) (b=0.13, p=0.10) or a fixed sleep period (n=68) (b=−0.14, p=0.24) (Figure 6).
Association of mean age of participants with total sleep time (min) for studies conducted between 1960–1989 (open circles) and 1990–2013 (closed circles).
Association of year of study with age-adjusted total sleep time (min) for all data points. The regression line and 95% confidence intervals are displayed.
Association of year of study with total sleep time (with regression line and 95% confidence intervals) for participants ages 18–27 years (a), 28–37 years (b), 38–47 years (c), 48–57 years (d), 58–67 years (e), 68–77 years (f), and ≥78 years (g).
Association of year of study with age-adjusted total sleep time (min) for polysomnographic data (a) and actigraphic data (b). The regression line and 95% confidence intervals are displayed.
Association of year of study with age-adjusted total sleep time (min) for women subjects only. The regression line and 95% confidence intervals are displayed.
Discussion
The results indicate relative stability of objectively-recorded sleep durations in healthy sleepers assessed over the last half-century. Similar results were found across all age groups; in both men and women; for both PSG and actigraphic data; and under conditions of fixed sleep periods and participants’ usual sleep schedules. These data are consistent with recent comprehensive reviews that found no consistent or compelling evidence of significant decrements in self-reported sleep duration and/or prevalence of short sleep over a similar range of years [11–15]. Together, these data cast doubt on the notion of a modern epidemic of insufficient sleep.
There were several limitations of the literature, which might have confounded demonstration of temporal changes in sleep duration. First, although virtually all of the studies failed to describe the racial/ethnic composition of the samples, it is a reasonable assumption that participants in most of these studies were not representative of the population. Recent research has suggested that the prevalence of short sleep is relatively high among Blacks, and that this prevalence might be increasing more among Blacks than among Whites [22]. Furthermore, most of the studies either excluded women or failed to report separate data for women and men. Thus, there was an insufficient number of data points (n=17) to adequately assess whether there was a temporal decline in women’s sleep duration, which might have occurred as more women have entered the workforce over the past 50 years [11, 15]. Study samples have also likely been unrepresentative of the population in other factors which have been associated with sleep duration, including employment status, education, occupation, and socioeconomic status.
A second limitation is that most of the studies assessed sleep with PSG in the laboratory, a process that can result in curtailed sleep duration. The confound was reduced in most of the PSG studies by disregarding data obtained during the first night of laboratory recording (eliminating “first night effects”) [23]. Interestingly, in a post-hoc assessment of studies that measured sleep objectively both at home and in the laboratory, the median difference between home and laboratory TST was only 3.2 min (Table 3). However, the use of PSG recording could have inhibited sleep, and sleep might have been more disrupted in earlier PSG studies due to greater novelty associated with PSG, as well as less technologically advanced methods, such as the use of collodion for securing electrodes.
Table 3
Studies located which assessed sleep objectively both at home and in the laboratory.
| Authors /Year | n | Home TST | Lab TST | Comments |
|---|---|---|---|---|
| Coates et al., 1979 | 8 | 380.8 | 364.1 | |
| Riley, Peterson, 1983 | 10 | 378 | 408 | |
| Edinger et al. 1997 | 32 | Nt 2,3: 371.8 | Nights 2–3: 361.1 | |
| Edinger et al., 2001 | 35 | Nt 2,3: 377.6 | Nights2–3: 376.5 | |
| Edinger et al, 2003 | 35 | 379.6 | 370.5 | |
| Means et al, 2003 | 49 | 376.6 | 371.2 | |
| Penev, 2007 | 12 | 381 | 383 | |
| Kobayashi, et al., 2012 | 22 | 373.1 | 403.7 | Actigraphy home PSG lab |
Constraints of PSG recording might not capture a decline in nighttime sleep that has occurred at home when people are more able to follow their customary habits, which might involve staying up later. Roenneberg et al.’s surveys of thousands of adults assessed from 2002–2010 have found a decline of approximately 30 min in reported sleep duration on weekdays [24]. However, the present review did not find a similar change in home actigraphic sleep duration over the past 10–20 years. Likewise, a recent study by Gubelmann et al. found no decline in reported time in bed from 2005–2011 among a large Swiss sample (n=3,853) [25].
A third limitation is that studies with fixed sleep periods (usually 8 h) could have resulted in sleep restriction for some individuals, particularly if the timing of the sleep periods was not consistent with the participants’ usual sleep schedule. This restriction could have been generally greater in earlier studies if sleep duration truly had declined. However, a similar age-adjusted mean TST was observed for studies involving fixed (443.3±31.7 min) and habitual sleep schedules (435.1±37.4 min), and there was a similar absence of a significant secular trend in TST for fixed and habitual sleep schedules (Figure 6). Figure 6A might reflect a societally-imposed or custom-imposed 8-hr ceiling in how long people usually spend sleeping. It is also possible that PSG technicians have been reluctant to extend the night shift beyond 8 h.
A fourth limitation is that compared with more recent studies, it is possible that earlier studies did not screen as well for absence of sleep apnea and other sleep disorders; this difference in screening methods might have resulted in lower estimates of sleep duration. However among adults above middle age, a small amount of sleep apnea or periodic limb movements is so common that it might be considered normal. Relatively more drug studies in recent years could have contributed to more extensive participant screening of normal sleepers, resulting in samples that sleep longer than population norms. However, a similar absence of a decline in sleep duration was found in the 18–27 year old adults, for whom the prevalence of sleep apnea and other health problems is relatively low. Also contrary to the hypothesis that more recent studies have had more homogenous samples of good sleepers, a post-hoc analysis showed no significant correlation between year of study and sample standard deviation of TST (r=−0.01).
A fifth limitation is that mean nighttime sleep duration data for a sample might not reflect temporal changes in the prevalence of short or long sleep, nor changes in 24-hr sleep duration which might have occurred. Interestingly, Figures 1–3 suggest a higher prevalence of sleep of ≤6 h over the last 20 years, particularly among 18–27 year old participants.
In recent decades, the siesta tradition has waned considerably in some countries [26]. Without corresponding increases in nighttime sleep, this could have resulted in a temporal decline in 24-h sleep in these countries. Partial support for this hypothesis was provided by Bin et al., who found in a meta-analysis that 24-h sleep duration decreased by 22 min from 1989–2002 in Italy [13], whereas there was not a decline in 24-h sleep in 8 of the other 9 countries assessed, none of which has had a notable siesta tradition (Australia, Canada, Finland, Germany, Netherlands, Norway, Sweden, United Kingdom, United States).
However, there has been limited empirical investigation of temporal trends in napping. Wolf-Meyer traces a historical decline in napping to the industrial revolution, increased structure of the work day, and the origins of sleep medicine which has promoted a theoretical need for 8 hours of sleep at night [27, 28]. Thus, through much of the 20th century, napping in many industrialized countries was regarded as a sign of laziness [28]. However, attitudes and practices of napping have apparently changed over the past 10–20 years, as evidenced by formal sanctioning of work-day napping and commercial napping services in some cities.
Napping is relatively more common among older adults who have less nighttime sleep and less consolidation of the sleep-wake cycle than young adults. Compared with previous older cohorts, some factors could have resulted in less napping in contemporary seniors, such as later retirement age, more physically and socially active lifestyles, and greater rates of residence in senior living facilities.
Nonetheless, the present review is the first to explore historical patterns of objective sleep duration, which has long been regarded as the gold standard for defining sleep duration [18]. Further, the findings have several implications. Although historically 8 h of sleep was thought to be optimal for health and well-being, an extensive epidemiologic literature has indicated that 7 h of self-reported sleep is associated with the lowest health risks [29], with progressively higher risks associated with shorter as well as longer reported sleep. However, since objectively-recorded sleep duration is generally 30–60 min less than self-reported sleep, optimal objective sleep duration for longevity and health might be only 6–6.5 h. For example, Kripke et al. recently found 5–6.5 h of actigraphic sleep was associated with lower mortality than <5 h and > 6.5 h [30]. The present review adds to recent reviews of self-reported data, which have also indicated no decline in sleep duration over the last 50 years. If the optimal duration of objective sleep is indeed between 6–6.5 hours, the review also suggests that more participants in these studies might be at risk due to long sleep than to short sleep.
Had sleep duration truly declined by 1–2 hours over the last 50 years, as many sleep researchers have claimed, the signal to detect this would be at least as great as that associated with age, which shows only a decline of about 1 h from young adulthood to the elderly (Figure 1). The results also contradict the hypothesis that such a decline in sleep is a probable culprit in modern epidemics of obesity and diabetes [21].
Notwithstanding these findings, assumptions about a steady decline in sleep duration over the past few decades persist, and could be explained by many factors. First, increased public awareness about sleep and the dangers of inadequate sleep, coinciding with an exponential increase in sleep disorders diagnoses with the emergence of sleep medicine [31], could have partly shaped these perceptions. Greater knowledge about sleep, perhaps especially a greater ability to distinguish between sleep and time spent in bed, could lead to perceptions of less sleep.
Second, sleep is commonly considered in the context of leisure time and being a respite from daily stressors [32]. In what seems to many to be an increasingly fast-paced and stressful world, there is a perception of having less free time for “rest.” Third, evidence indicates that the prevalence of depression has increased over time [33], and depression is associated with reports of poor or inadequate sleep [34].
Fourth, self-reported behavior is influenced by perceived social norms [26, 35], and the perception that we have become a sleep-deprived society has likely been shaped partly by promotion of this message in the popular media and by sleep scientists. However, much of the narrative regarding an epidemic of declining sleep has been based on arguments which have not been well-supported by empirical data. We address some of these arguments in the following section, although much of this discussion is also not well-supported by empirical observations.
Decline of Sleep in Children?
A particularly poignant argument for an epidemic of insufficient sleep is that sleep among children and adolescents has declined, due to many factors, including greater use of electronic media at night and reduced parental enforcement of bedtimes. The fear that children are sleeping less has apparently existed for over a century [36], and in recent years this fear may have contributed to the increased rates of hypnotic prescriptions for children [37].
A recent empirical review by Matricciani et al. found that reported sleep duration of children and adolescents has declined by an average of 70 min per night since 1895 [38]. However, these data should be considered within the context of the tremendous difference in physical activity levels of modern children compared with children of over a century ago who were required to work on family farms, and for 60 h per week in mines, sweatshops, factories, etc. [39]. The Matricciani et al. review found that reported sleep duration of children and adolescents has declined by only about 15 min per night since 1970 [38], and this difference could also be partly explained by dramatic declines in children’s physical activity levels during this period of time, as walking/cycling to school and playing outdoors have been largely replaced by car rides and sedentary indoor activities [40]. Changes in reported sleep duration of children should be verified with a review of objective sleep data analogous to the present review.
Twenty-four hour society?
The cliché of an ever-expanding 24/7 society [41] is not well-supported by empirical evidence, at least not over the past 50 years. For example, evidence suggests that the prevalence of shift-work has remained stable at about 15–20% over this interval of years [42, 43]. Such data might seem counterintuitive in light of the increased number of 24-h services and businesses. However, while many of these businesses (e.g, restaurants and convenience stores) can operate all-night with just a few employees, over the past half-century there has been a dramatic disappearance of factories which once employed thousands of shift-workers. Moreover, over the past 10–20 years, protective regulations and practices which limit shift-work and sleep deprivation and/or better accommodate individual’s preferences (e.g,. flex time and telecommuting), have been implemented for various occupations, including medical residents, truck drivers, and transportation workers [44, 45].
A Decline in Sleep Over the Centuries?
It is a widely repeated hyperbole that never before in human history have we faced such challenges to our sleep [46]. It has been hypothesized that industrialization, urbanization, and technological advances have caused us to ignore or override our natural tendency to sleep more, and we do so at great costs to our health and quality of life. Wolf-Meyer has noted that this “fall from grace” sentiment can be traced back at least as far as the pioneering work of Nathaniel Kleitman [27, 28]. However, historical accounts belie the myth that people slept longer or better centuries ago, when sleep was compromised by pestilence, fear of night marauders, poorer ability to control ambient temperature or treat illnesses, etc. [28, 47]. By Ekirch’s estimation, sleep centuries ago typically occurred in two nighttime in-bed periods, with each period lasting approximately 3–4 h, suggesting that average sleep duration probably did not exceed 7 h (personal communication) [48].
The light bulb has been blamed for sleep loss [49]. However, recent anthropologic studies of people in societies with little or no electricity have failed to indicate that these people sleep more than people in industrialized societies [50, 51].
In summary, it is beyond dispute that disrupted and inadequate sleep are highly prevalent and associated with significant risks, and that experimental sleep deprivation has myriad negative effects [52, 53]. Thus, the notion of a recent epidemic of insufficient sleep, and speculation that this is a primary contributor to modern epidemics of obesity, diabetes, metabolic syndrome, etc., rests largely on the question of whether sleep duration has declined in the last few decades. Consistent with recent reviews of subjective data [11–15, 54], this review does not support this notion, at least not in healthy sleepers
Acknowledgments
This manuscript is dedicated to Dr. Richard R. Bootzin, our dear friend and colleague who passed away on December 4, 2014. Dr. Bootzin contributed to earlier drafts of this manuscript. Research supported by RO1-HL095799; R01-MD007716; R01-AG034588; R01-AG026364; R01-CA160245; R01-DA032922 the Cousins Center for Psychoneuroimmunology. Susan Noh assisted with this study.
List of Abbreviations
| PSG | polysomnography |
| TIB | time in bed |
| TST | total sleep time |
Footnotes
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