TOPICS
Anti-malondialdehyde-acetaldehyde adducts antibodies in lung tissues may play important role in pathogenesis of RA-associated interstitial lung disease, study indicates
By Dr Deepu
Anti-malondialdehyde-acetaldehyde adducts (MAA) antibodies and MAA expression in lung tissues of patients with rheumatoid arthritis-associated interstitial lung disease (RA-ILD) likely play an important role in RA-ILD pathogenesis, and anti-MAA antibodies may function well as serum biomarkers in the identification of this disease manifestation.
Patients with RA face premature mortality and RA-ILD is a major determinant of worse long-term outcomes, with a median survival as short as 3 years after diagnosis. In the present study, researchers compared serum anti-MAA antibodies and MAA expression in lung tissues of patients from 13 sites fulfilling the 1987 American College of Rheumatology criteria by selecting participants from the Veterans Affairs Rheumatoid Arthritis Registry.
Multivariable logistic regression models were used to assess the association between anti-MAA antibodies (immunoglobulins A, M, and G [IgA, IgM, IgG]) and RA-ILD status by combining RA alone with RA+chronic obstructive pulmonary disease (COPD) for a comparator group, as unadjusted comparisons found no significant differences in concentrations of anti-MAA antibodies between these groups. Lung tissues from RA-ILD patients, and other patients with ILD, emphysema, and controls were stained for MAA, macrophages (CD68), citrulline, B cells (CD19/CD27), T cells (CD3), and extracellular matrix proteins (fibronectin, vimentin, type-II collagen). Lung tissue expression and MAA co-localization were quantified and compared.
Among the total 1823 participants with RA, 90 had RA-ILD. Higher serum concentrations of IgM and IgA anti-MAA antibodies were seen in RA-ILD vs RA+COPD or RA alone (P =.005). After adjustment for covariates, the highest quartiles of IgM (odds ratio [OR] 2.23; 95% CI, 1.19-4.15) and IgA (OR 2.09; 95% CI, 1.11-3.90) anti-MAA antibody were significantly associated with RA-ILD. MAA expression in lung tissue was greater in RA-ILD than all other groups (P <.001). The RA-ILD group also showed the greatest degree of MAA co-localized with CD19+ B cells (r =0.78), citrulline (r =0.79), and extracellular matrix proteins (type-II collagen [r =0.72] and vimentin [r =0.77]).
The study authors concluded the study by noting "These findings suggest that MAA immune responses could play an important role in the pathogenesis of RA-ILD and anti-MAA antibodies may be promising serum biomarkers in the identification of this extra-articular disease manifestation"
The finding were published in arthritis and rheumatology
Many children with asthma do not use inhalers properly, study indicates
By Dr Deepu
Research indicates “many children with asthma don’t use their inhalers properly and don’t get a full dose of medicine.” Investigators looked at “inhaler use among 113 children between the ages of 2 and 16 who were hospitalized for asthma.” The researchers found that “at least one crucial step in inhaler technique was missed by 42% of the children,” and approximately “18% did not use a spacer device with their inhaler.” The findings were published in the Journal of Hospital Medicine.
Research indicates “many children with asthma don’t use their inhalers properly and don’t get a full dose of medicine.” Investigators looked at “inhaler use among 113 children between the ages of 2 and 16 who were hospitalized for asthma.” The researchers found that “at least one crucial step in inhaler technique was missed by 42% of the children,” and approximately “18% did not use a spacer device with their inhaler.” The findings were published in the Journal of Hospital Medicine.
Tuberculosis could be eliminated by 2045, researchers suggest
By Dr Deepu
A new study by researchers suggests that “increased investment in evidence-based interventions
to diagnose, treat, and prevent tuberculosis (TB), especially in high-burden
countries, could help end TB” by the year 2045. These interventions should not
only “be scaled up, but greater investment and research is needed to develop
new methods of diagnosis, treatment, and prevention around the world,
[researchers] reported.” Additionally, they suggest that “responsibility for
investing in TB programs should be shared between domestic allocation in these
countries, as well as external funding through increased developmental assistance.”
The authors mentioned that”to reach these goals, global
investment in TB research and development will need to increase to at least $2
billion per year during the next 4 years”.
With the goals of treating 40 million people and preventing
30 million new cases from 2018-2022, the United Nations held its first-ever
"high-level meeting" about TB,in September 2018
A TB-free world is possible by 2045 if "increased
political will and financial resources" are targeted towards areas where
they are needed most, as stated in the report
In India, the country
with the highest burden of TB, "unavoidable tuberculosis deaths"
will cost the country at least $32 billion each year over the next 30 years,
even with "optimal implementation of existing tools." The authors also
have mentioned that the savings from averting a TB death can be three times the
costs in certain countries.
Tuberculosis was declared a global emergency by WHO in 1993.
Then, about a third of the world’s population was infected with the bacteria
that cause tuberculosis, and the disease was responsible for an estimated 3
million deaths each year. Today, around a quarter of the world’s population has
a tuberculosis infection, which causes about 1·6 million annual deaths, making
it the leading infectious killer of our time. Although progress has been made
in reducing the global burden of tuberculosis in the past 25 years, it has
occurred at a frustratingly slow rate. Declines in tuberculosis mortality are
not keeping pace with reductions in deaths from other infectious diseases of
global importance such as HIV and malaria, and the world is not on track to
meet targets set out in the Sustainable Development Goals and the WHO End TB
Strategy.
The findings were published in The Lancet.
Statins in Asthma COPD overlap may bring down the risk of CAD and stroke risk
By Dr Deepu
Recently published study in atherosclerosis journal has found
that the risk for CAD was lower in all statin-treated patients with ACOS. Whereas
the risk for ischemic stroke was lower only in long-term statin users with ACOS.
There was no link between risk for
hemorrhagic stroke and statin use.
A retrospective cohort study was conducted using data from
the Longitudinal Health Insurance Database, which included 1 million enrollees
in the Taiwan National Health Insurance program from January 1, 2000, through
December 31, 2011.
Patients ≥20 years of age with ACOS who were treated with
statins (n=916) and those who did not receive statin therapy (n=6338) were
enrolled in the study. Investigators examined the cumulative incidence of CAD
and stroke (both ischemic and hemorrhagic) with the use of time-dependent Cox
proportional regression. Following adjustments for age, sex, inhaled corticosteroid
use, oral steroid use, and comorbidities, adjusted hazard ratios (aHRs) and 95%
CIs for CAD or stroke in statin users (long-term statin use: >600 days;
short-term statin use: ≤600 days) were compared with these values in statin
nonusers.
In statin users, the aHRs for CAD and stroke were 0.50 (95%
CI, 0.41-0.62) and 0.83 (95% CI, 0.63-1.09), respectively. Furthermore, aHRs
for ischemic and hemorrhagic stroke were 0.30 (95% CI, 0.09-0.99) and 0.90 (95%
CI, 0.68-1.20), respectively. In addition, in long-term statin users, aHRs for
CAD and stroke were 0.23 (95% CI, 0.13-0.41) and 0.42 (95% CI, 0.19-0.89),
respectively. In short-term statin users, aHRs for CAD and stroke were 0.58
(95% CI, 0.47-0.71) and 0.93 (95% CI, 0.70-1.23), respectively.
A major limitation of the current study is that lipid levels
were not taken into account. Moreover, although a new-user study design was
employed, with propensity score matching and a time-dependent model for
analysis, results were not as accurate as those derived from randomized
controlled trials.
The investigators concluded that regardless of the duration
of statin use, the risk for CAD was lower in all
statin-treated patients with ACOS. In contrast, the risk for ischemic stroke
was lower only in long-term statin users with ACOS, and no link was observed
between risk for hemorrhagic stroke and use of statin therapy.
The study was published in atherosclerosis journal
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