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Association of phthalate exposure and airway dysfunction, with mediation by serum periostin
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Background: Phthalates can cause respiratory and immunological
disorders. However, little is known about the role of serum periostin
and YKL-40 levels in mediating the effects of phthalates. We
investigated the mediating role of these biomarkers in the relationship
between phthalates and airway dysfunction. Methods: A total of 487
children (aged 10 to 12 years-old) were examined. Four
high-molecular-weight phthalate (HMWP) [Σ4HMWP] metabolites and 3
low-molecular-weight phthalate (LMWP) [Σ3LMWP] metabolites in urine
samples were measured. Serum periostin and YKL-40 levels were measured.
Airway function was measured using impulse oscillometry. A mediation
model was used to quantify the mediating effects of periostin and YKL-40
on airway dysfunction. Results: After adjustment for height, gender, BMI
z-score, aeroallergen sensitization, secondary smoking, and vitamin D
level, the level of urinary Σ3LMWP metabolites was significantly
associated with respiratory system resistance at 5 Hz (Rrs5; adjusted β:
0.020, 95% CI: 0.005 to 0.034; P = .010). The levels of urinary Σ4HMWP
and Σ3LMWP metabolites were significantly associated with periostin
level, but not with YKL-40 level. In addition, the periostin level was
associated with Rrs5 (adjusted β: 0.048, 95% CI: 0.015 to 0.081; P =
.005) and Rrs20-5 (adjusted β: 0.040, 95% CI: 0.011 to 0.069; P =.007).
Serum periostin level had a significant effect in mediating the
relationship between Σ3LMWP and Rrs5 (13.9%, 95% CI: 10.7 to 77.0; P
< .001). Conclusion: Exposure to LMWPs was significantly
associated with airway dysfunction, and this effect was partially
attributable to increased serum periostin level.
Title: Association of phthalate exposure and airway dysfunction, with mediation by serum periostin
Description:
Background: Phthalates can cause respiratory and immunological
disorders.
However, little is known about the role of serum periostin
and YKL-40 levels in mediating the effects of phthalates.
We
investigated the mediating role of these biomarkers in the relationship
between phthalates and airway dysfunction.
Methods: A total of 487
children (aged 10 to 12 years-old) were examined.
Four
high-molecular-weight phthalate (HMWP) [Σ4HMWP] metabolites and 3
low-molecular-weight phthalate (LMWP) [Σ3LMWP] metabolites in urine
samples were measured.
Serum periostin and YKL-40 levels were measured.
Airway function was measured using impulse oscillometry.
A mediation
model was used to quantify the mediating effects of periostin and YKL-40
on airway dysfunction.
Results: After adjustment for height, gender, BMI
z-score, aeroallergen sensitization, secondary smoking, and vitamin D
level, the level of urinary Σ3LMWP metabolites was significantly
associated with respiratory system resistance at 5 Hz (Rrs5; adjusted β:
0.
020, 95% CI: 0.
005 to 0.
034; P = .
010).
The levels of urinary Σ4HMWP
and Σ3LMWP metabolites were significantly associated with periostin
level, but not with YKL-40 level.
In addition, the periostin level was
associated with Rrs5 (adjusted β: 0.
048, 95% CI: 0.
015 to 0.
081; P =
.
005) and Rrs20-5 (adjusted β: 0.
040, 95% CI: 0.
011 to 0.
069; P =.
007).
Serum periostin level had a significant effect in mediating the
relationship between Σ3LMWP and Rrs5 (13.
9%, 95% CI: 10.
7 to 77.
0; P
< .
001).
Conclusion: Exposure to LMWPs was significantly
associated with airway dysfunction, and this effect was partially
attributable to increased serum periostin level.
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