Table 7 Human studies on NSW and telomeres length and aging

From: Night shift work and breast cancer: from etiopathology to precision risk analysis

NSW Effect

Parameter(s)

Outcome

Year

Ref.

Slight shortening of TL, more pronounced in postmenopausal women

Leukocyte relative TL (LTL, blood)

↓ TL

2011

237

Trend toward shorter TL with longer NSW history (not significant)

Peripheral blood leukocyte TL (PBL TL, blood)

↓ TL (ns)

2011

238

Intensive consecutive NSW ( ≥ 4–6 nights for ≥5 yrs) associated with shortened TL and higher BC risk

TL (saliva DNA)

↓ TL

2017

239

NSW associated with higher CRP (systemic inflammation), LTL positively correlated with PTX3 (protective)

LTL (blood), plasma PTX3, CRP

↑ (PTX3), ↑ CRP → potential ↓ TL

2017

144

Cumulative NSW: <12 yrs associated with longer TL, ≥12 yrs with shorter TL

TL (blood)

↑ ( < 12 yrs), ↓ ( ≥ 12 yrs)

2019

227

NSW modifies effect of sleep disturbances on epigenetic ageing

AgeDevGrim and DunedinPACE clocks

↑ TL (with insomnia/sleep deprivation)

2025

240

Prolonged NSW associated with shorter TL; partial reversal after cessation; DNA methylation AA unchanged

TL (blood), DNA methylation-based age acceleration

↓ TL, no change AA

2025

241

  1. NSW night shift work, TL telomere length, LTL leukocyte TL, PBL TL peripheral blood leukocyte TL, BC breast cancer, CRP C-reactive protein, PTX3 pentraxin 3, AA age acceleration, AgeDevGrim Age Deviation GrimAge epigenetic clock, DunedinPACE Dunedin PoAm / Accelerated Pace of Aging epigenetic clock. Arrows indicate direction of change relative to day workers ( ↑ increase; ↓ decrease; ↔ no change, → consequential change).