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“showed a trend”

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Other osteogenesis-associated genes (ALP, OCN, and Col1a) were not significantly expressed on day 7; however, they showed a trend similar to that of Runx2 and osterix on day 14. 3.3 Ectopic osteogenesis in muscle pouch 3.3.1 X-ray and EDS spectrum analysis The results showed that images of implants in the T0 group were almost uncaptured at all time points, whereas the images of implants in groups T5, T6, T7, and T8 exhibited varying degrees of mineralization with increasing time ( Fig. 4 a).
They showed a trend toward reduction of MI, TLF, and stent thrombosis (ST) for patients treated with BP‐SES. 14 Zhu et al. considered six RCTs comparing BP‐SES with two different durable polymer stents for the meta‐analysis, in which a significantly reduced risk for MI in BP‐SES treated subjects was found. 15 As the majority of these analyses was performed at publication level, detailed analyses of different patient subgroups were not possible.
4.3 Exposure–response for safety While the exposure–unbound E2 relationship showed a trend of lower E2 with increasing vilaprisan exposure, the E2 concentrations mostly remained within the physiologic range for the follicular phase and E2 levels returned to baseline for all patients in both ASTEROID 1 8 and ASTEROID 2. 9 Although a decrease in E2 levels will contribute to ovulation inhibition and consequently to induction of amenorrhoea, 6 the potential effect of a decrease in E2 levels on long‐term safety is considered to be of higher clinical relevance.
Previous and recent multicenter, randomized controlled trials showed a trend towards reduced mortality in favor of V‐V ECMO over conventional treatment. 6 , 7 Furthermore, in a recently published meta‐analysis of these trials, 60‐day mortality was significantly lower in the V‐V ECMO group. 8 Although mortality rates in V‐V ECMO are lower compared with other ECMO modalities, a substantial quote of patients still die during hospital admittance. 9 According to the Extracorporeal Life Support Organization (ELSO), more than 75 000 ECMO runs for respiratory compromise have been performed in more than 450 centers (as of July 2021).
In general, during the entire drought period, S‐D showed a trend towards lower values than L‐D (Figure S4 ), but no statistical differences were observed at any date of measurement. 3.3 Rewatering period Since irrigation was re‐started at different times for L‐D and S‐D containers, we present the g s and A N data in parallel as days of rewatering (DOR) to permit a direct comparison between L and S (Figure 3 ).
In addition, mRNA-vaccinated patients who were treated with thiopurines showed a trend towards lower antibody concentrations compared to patients who were not treated with thiopurines (geometric mean [95% confidence interval]: 4523 [3574-5724] vs . 5634 [4561-6958] AU/ml, P=0.182).
When compared to the RP240 model, the RP340 model showed a trend of improved correlation with the manual grading for the measurement of EZ width (correlation coefficient changed to 0.988 from 0.981), increased linear regression slope (changed to 0.951 from 0.930), and reduced CoR (changed to 0.582 mm from 0.728 mm).
Similar to the HCRU, the overall annual HCRU direct cost also showed a trend toward highest mean AD-related HCRU gross cost (per patient) among moderate-to-severe treated AD cohort (531.5 USD) followed by the mild-to-moderate treated AD cohort (378.4 USD) and lowest for the untreated AD cohort (144.0 USD).
r antagonists, renin–angiotensin–aldosterone system inhibitors and angiotensin receptor neprilysin inhibitor (ARNI) might be used for patients with mildly reduced left ventricular ejection fraction ( HFmrEF; 41–49%), but with a IIB class of recommendation.[ 1 ] Indeed, the PARAGON-HF trial recently showed a trend towards better outcomes in HFpEF patients treated with sacubitril/valsartan (an ARNI) compared to valsartan, especially in the lower end of the left ventricular ejection fraction (LVEF) spectrum, in women, in patients recently hospitalised for HF, and in those with higher high sensitivity troponin values at baseline.[ 3 – 7 ] However, while the Food and Drug Administration has approved sacubitril/valsartan use in patients with ‘below normal’ LVEF, the European Medicines Agency has not.