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. Author manuscript; available in PMC: 2017 Sep 1.
Published in final edited form as: J Matern Fetal Neonatal Med. 2015 Nov 26;29(17):2767–2772. doi: 10.3109/14767058.2015.1103224

Table 2.

Interaction between Placental Telomere Length (PTL) and Mitochondrial DNA Copy Number (mtDNA CN) on Risk of Placental Abruption (PA)

PA Cases (N=105) Controls (N=73) Stratified Analysis Joint Analysis

Unadjusted OR (95% CI) Adjusted OR (95% CI)* Unadjusted OR (95% CI) Adjusted OR (95% CI)*

Below median mtDNA CN, Above median placental telomere length 18 22 1.00 (reference) 1.00 (reference) 1.00 (reference) 1.00 (reference)
Below median mtDNA CN, Below median placental telomere length 31 14 2.71 (1.12, 6.57) 3.07 (1.13, 8.38) 2.71 (1.12, 6.57) 3.11 (1.17, 8.30)
Above median mtDNA CN, Above median placental telomere length 26 15 1.00 (reference) 1.00 (reference) 2.12 (0.87, 5.16) 2.25 (0.84, 6.00)
Above median mtDNA CN, Below median placental telomere length 30 22 0.79 (0.34, 1.82) 0.71 (0.28, 1.83) 1.67 (0.73, 3.83) 1.61 (0.64, 4.05)
P-value for interaction 0.048 0.032
*

Adjusted for maternal age, gestational age at delivery, mode of delivery, and pre-pregnancy body mass index.

Placental mtDNA copy number: Low: < median (< 84.92) in primary period of collection and (<102.53) in secondary period of collection; high: ≥ median (≥84.92) in primary period of collection and (≥102.53) in secondary period of collection. Placental telomere length: high: ≥ median (≥2.32) in batch 1 and (≥1.42) in batch 2; low: < median (<2.32) in batch 1 and (<1.42) in batch 2.