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Nearly one in six women with infertility in Hong Kong had used CBRC. Among women who had not used CBRC, more than one third planned to use or would consider it. The main factors influencing the likelihood of CBRC use were long waiting times in the public sector and high cost in the private sector. These results will help clinicians to more effectively counsel patients considering CBRC and facilitate infertility services planning by authorities in Hong Kong.
Nearly one in six women with infertility in Hong Kong had used CBRC. Among women who had not used CBRC, more than one third planned to use or would consider it. The main factors influencing the likelihood of CBRC use were long waiting times in the public sector and high cost in the private sector. These results will help clinicians to more effectively counsel patients considering CBRC and facilitate infertility services planning by authorities in Hong Kong.
To assess whether gene expression signatures associated with rheumatoid arthritis (RA) before pregnancy differ between women who improve or worsen during pregnancy, and determine whether these expression signatures are altered during pregnancy when RA improves or worsens.
Clinical data and blood samples were collected before pregnancy (T0) and at the third trimester (T3) from 11 RA and 5 healthy women. RA disease activity was assessed using the Clinical Disease Activity Index (CDAI). At each time-point, RA-associated gene expression signatures were identified using differential expression analysis of RNA sequencing profiles between RA and healthy women.
Of the women with RA, 6 improved by T3 (RA
), 3 worsened (RA
) and 2 were excluded. At T0, mean CDAI scores were similar in both groups (RA
11.2±9.8; RA
13.8±6.7; Wilcoxon-rank test p=0.6). In the RA
group, 89 genes were differentially expressed at T0 (q<0.05 and fold-change (FC)≥2) compared to healthy women. Iruplinalkib purchase When RA improved at T3, 65 of 89 (73%) of these no longer displayed RA-associated expression. In the RA
group, a largely different RA gene expression signature (429 genes) was identified at T0. When RA disease activity worsened at T3, 207 of 429 (48%) lost their differential expression, while an additional 157 genes became newly differentially expressed.
In our pilot dataset, pre-pregnancy RA expression signatures differed between women who subsequently improved or worsened during pregnancy, suggesting that inherent genomic differences perhaps influence how pregnancy impacts disease activity. Further, these RA signatures were altered during pregnancy, as disease activity changed.
In our pilot dataset, pre-pregnancy RA expression signatures differed between women who subsequently improved or worsened during pregnancy, suggesting that inherent genomic differences perhaps influence how pregnancy impacts disease activity. Further, these RA signatures were altered during pregnancy, as disease activity changed.
To compare the CDAI with the RAPID3 from two large US Registries.
Using a cross section of clinic visits within two registries we determined if the outcome of each metric would place the patient in remission (R), low (LDA), moderate (MDA), or high disease activity (HDA) using a CDAI with the assumption that a patient in MDA or HDA would be a candidate for acceleration of treatment.
We identified significant disparities between the two indices in final disease categorization using each index system. For patients identified in LDA by CDAI, RAPID3 identified 20.4% and 28.3% as LDA in Corrona and BRASS respectively. For patients identified as MDA by CDAI, RAPID3 identified 36.2% and 31.1% as MDA in Corrona and BRASS respectively with the greatest disparities within each system identified for LDA and MDA activity by the CDAI (20.4% and 36.2% agreement of RAPID3 with CDAI respectively in Corrona and 28.3% and 31.1% agreement in BRASS). Overall comparison between CDAI and RAPID3 in the 4 disease categories resh CDAI respectively in Corrona and 28.3% and 31.1% agreement in BRASS). Overall comparison between CDAI and RAPID3 in the 4 disease categories resulted in estimated Kappa=0.285 in both. The RAPID3 scores indicated the potential for treat to target acceleration in 34.4% of patients in remission or LDA based on CDAI in Corrona and 27.6% in BRASS respectively CONCLUSION The RAPID3, based on patient reported outcomes, shows differences with CDAI categories of disease activity. The components of CDAI are not highly correlated with RAPID3 except for patient global. These differences could significantly impact the decision to advance treatment when using a treat to target regimen.
To evaluate the impact of comorbid conditions on direct health care expenditure and work-related outcomes in patients with rheumatoid arthritis (RA).
This was a retrospective analysis of the Medical Expenditure Panel Survey from 2006 to 2015 in 4,967 adult RA patients in the USA. Generalised linear models were used for health care expenditure and income, logistic model for employment status, and zero-inflated negative binomial model for absenteeism. Thirteen comorbid conditions were included as potential predictors of direct cost and work-related outcomes. The models were adjusted for sociodemographic factors including sex, age, region, marital status, race/ethnicity, income, education and smoking status.
RA patients with heart failure had the highest incremental annual health care expenditure (US$8,205; 95% CI, US$3,683-US$12,726) compared to those without the condition. Many comorbid conditions including hypertension, diabetes, depression, obstructive pulmonary disease, cancer, stroke and heart failure lowest likelihood of being employed compared to other common comorbid conditions.
To study differences in pain reports between patients with ankylosing spondylitis (AS) and non-radiographic axial spondyloarthritis (nr-axSpA), and to assess how pain sensitivity measures associate with disease and health outcomes.
Consecutive patients with axial SpA (axSpA) were enrolled in the populationbased SPARTAKUS cohort (2015‒2017), and classified as AS (n=120) or nr-axSpA (n=55). Pain was assessed with questionnaires (intensity/duration/distribution) and computerized cuff pressure algometry to measure pain sensitivity (pain threshold/pain tolerance/temporal summation of pain). Linear regression models were used to compare pain measures between AS and nr-axSpA patients, and to assess associations between pain sensitivity measures and disease and health outcomes.
Of 175 axSpA patients, 44% reported chronic widespread pain, with no significant differences in any questionnaire-derived or algometry-assessed pain measures between AS and nr-axSpA patients. Lower pain tolerance was associated with longer symptom duration, worse ASDAS-CRP, BASFI, and BASMI, more pain regions, unacceptable pain, worse MASES, fatigue, anxiety, and health-related quality of life.
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