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A study by Satizabal et al published
in the NEJM found that dementia rates
fell steadily over the past three decades, likely due to declining rates of
heart disease.
The study analyzed data
collected since 1975 from the Framingham Heart Study
and included 5205 persons 60 years of age or older. The authors compared interactions
between epoch and age, sex, apolipoprotein E ε4 status, educational level, as
well as the effects of vascular risk factors such as cardiovascular disease on the
prevalence of dementia.
The 5-year age-and sex-adjusted
cumulative hazard rates for dementia were 3.6 per 100 persons during the first
epoch (late 1970s and early 1980s), 2.8 per 100 persons during the second epoch
(late 1980s and early 1990s), 2.2 per 100 persons during the third epoch (late
1990s and early 2000s), and 2.0 per 100 persons during the fourth epoch (late
2000s and early 2010s). Relative to the incidence during the first epoch, the
incidence declined by 22%, 38%, and 44% during the second, third, and fourth
epochs, respectively. This risk reduction was observed only among persons who
had at least a high school diploma. The prevalence of most vascular risk
factors (except obesity and diabetes) and the risk of dementia associated with
stroke, atrial fibrillation, or heart failure have decreased over time, but
none of these trends completely explain the decrease in the incidence of the
disease.
The authors concluded that the
incidence of dementia has declined over the course of three decades.
N Engl J Med 2016; 374:523-532
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Friday, April 1, 2016
Decades long decline in Dementia
Tuesday, March 1, 2016
Cancer death rate has fallen in the United States
Each year, the American Cancer Society
(ACS) estimates the numbers of new cancer cases and deaths that will occur in
the United States in the current year and compiles the most recent data on
cancer incidence, mortality, and survival.
The ACS collects and reports data from
several registries such as SEER, CDC, NPCR, NACCR and NCHS. In 2016, 1,685,210 new cancer cases and
595,690 cancer deaths are projected to occur in the United States. Overall
cancer incidence trends are stable in women, but declining by 3.1% per year in
men (from 2009-2012), much of which is because of recent rapid declines in
prostate cancer diagnoses. The cancer
death rate has dropped by 23% since 1991, translating to more than 1.7 million
deaths averted through 2012. The decline is attributed to decreasing
smoking rates and advances in cancer detection, treatment and prevention.
Deaths from lung, breast, prostate, and colon/rectum cancers drove
overall declines. Death rates for female
breast cancer have declined 36% from peak rates in 1989, while deaths from
prostate and colorectal cancers have each dropped about 50% from their peak.
Meanwhile, lung cancer death rates declined 38% between 1990 and 2012 among
males and 13% between 2002 and 2012 among females, due to a decline in the use
of tobacco.
In spite of this progress, death rates
are increasing for cancers of the liver, pancreas, and uterine corpus. Among
children and adolescents (aged birth-19 years), brain cancer has surpassed
leukemia as the leading cause of cancer death because of the dramatic
therapeutic advances against leukemia.
Despite of these remarkable
improvements cancer remains the leading cause of death in 21 states, primarily
due to exceptionally large reductions in death from heart disease. Accelerating
progress against cancer requires novel approaches in diagnosis, treatment and the application of existing cancer control knowledge across all
segments of the population
CA: A Cancer J Clin Vol 66, 1, 7-30,
Jan-Feb 2016
Monday, February 1, 2016
One-third of all cancers maybe inherited
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Muci et al published in JAMA the results of a trial that suggests
that approximately one-third of all cancers are due to inherited genes.
The investigators
looked at data from 80 309 monozygotic and 123 382 same-sex dizygotic twin
individuals (N = 203 691) within the population-based registers of Denmark, Finland,
Norway, and Sweden, who were part of the Nordic Twin Study of Cancer.
Twins
were followed up a median of 32 years between 1943 and 2010. There were 50 990
individuals who died of any cause, and 3804 who emigrated and were lost to
follow-up.
The
main outcome was incident cancer and time-to-event analyses were used to
estimate familial risk.
A
total of 27 156 incident cancers were diagnosed in 23 980 individuals,
translating to a cumulative incidence of 32%. Cancer was diagnosed in both
twins among 1383 monozygotic (2766 individuals) and 1933 dizygotic (2866
individuals) pairs. Of these, 38% of monozygotic and 26% of dizygotic pairs
were diagnosed with the same cancer type.
The analysis of data found that overall heritability for cancer
was 33 percent among the entire study population, and significantly higher for
certain types of cancers. Significant
heritability was found in 58 percent of diagnosed skin melanomas, 57 percent of
prostate cancers, 43 percent of non-melanoma skin cancers, 39 percent of
ovarian cancers, 38 percent of kidney cancers, 31 percent of breast cancers and
27 percent of uterine cancers. In the
same study researchers identified a set of cancers in which genetics play a
very small role. This group includes lung cancer (18 percent), colon cancer (15
percent), rectal cancer (14 percent), and head and neck cancer (9 percent).”
In
this long-term follow-up study among Nordic twins, there was significant
familial risk for cancer overall and for specific types of cancer. This information about hereditary risks of
cancers may be helpful in patient education and cancer risk counseling.
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Friday, January 1, 2016
Top Three Posts
During the last two years I uploaded 20 posts in my blog
Medical News Monthly. The top three in
order of viewing frequency were:
1. Ebola Outbreak
2. The Mediterranean Diet
3. WHO Report on Antimicrobial
Resistance
Most of the visitors were from the United States,
followed by Greece, Russia, France, Macedonia, Poland, Ireland, Ukraine,
Germany, Switzerland and India in that order.
Tuesday, December 1, 2015
SPRINT trial redefines blood pressure targets
More than 70 million people in the United States suffer from hypertension – which presently is defined by a systolic blood pressure of higher than 140 mm Hg and a diastolic of higher than 90 mm Hg. A landmark study called SPRINT (Systolic Blood Pressure Intervention Trial) challenges the accepted guidelines of optimum level for systolic blood pressure and provided information about benefits and shortcomings of intensive pharmacotherapy. The study was published in NEJM was interrupted nearly two years early, when it became apparent that lower blood pressure for most people over 50 prevented heart problems and deaths.
In the SPRINT trial, 14,692 patients
were assessed for eligibility, and 9361 individuals with a systolic blood
pressure of 130 mm Hg or higher and an increased cardiovascular risk, but
without diabetes, were randomly assigned in two groups; a systolic
blood-pressure target group of less than 120 mm Hg (intensive treatment) or a
target group of less than 140 mm Hg (standard treatment).
The primary outcomes were myocardial
infarction, other acute coronary syndromes, stroke, heart failure, or death
from cardiovascular causes.
At 1 year, the mean systolic blood
pressure was 121.4 mm Hg in the intensive-treatment group and 136.2 mm Hg in
the standard-treatment group. The mean number of blood-pressure medications was
2.8 in the intensive-treatment group and 1.8 in the standard-treatment group. The intervention was stopped early after a
median follow-up of 3.26 years owing to a significantly lower rate of the
primary composite outcome in the intensive-treatment group than in the
standard-treatment group (1.65% per year vs. 2.19% per year; hazard ratio with
intensive treatment, 0.75; 95% confidence interval [CI], 0.64 to 0.89;
P<0.001). All-cause mortality was also significantly lower in the
intensive-treatment group (hazard ratio, 0.73; 95% CI, 0.60 to 0.90; P=0.003).
Investigators found that there were 27% fewer
deaths (155 compared with 210) and 38% fewer cases of heart failure (62
compared with 100) among patients who achieved the
systolic pressure target of 120 mm Hg than among those who achieved the current
140 mm Hg target.
The lower
relative risk of major cardiovascular events observed across subgroups defined
according to age, sex, race, medical history, and baseline blood pressure among
patients who achieved the systolic pressure target of 120 mm Hg in comparison
to those who achieved the currently recommended level of 140 mm Hg.
Rates of serious adverse events of
hypotension, syncope were 67% and 33% higher in the intensive therapy
group. Electrolyte abnormalities, and
acute kidney failure were noted but injuries due to falls surprisingly were not
more common, as had been feared among the elderly in the intensive-treatment
group.
The research indicated that among
patients over 50 at high risk for cardiovascular events who are not diabetics,
targeting a systolic blood pressure below the current guidelines of 140 or 150
mm Hg to less than 120 mm Hg, prevented heart disease and strokes and thus save
lives.
DOI:
10.1056/NEJMoa1511939
Sunday, November 1, 2015
Breast Cancer Screening for Women at Average Risk
Breast cancer is a leading cause of
mortality among US women. About 200,000 women are being diagnosed every
year in the US with breast cancer and 40,000 women die from the disease.
Despite the interest and research
on breast cancer screening, there is uncertainty about mammography’s benefits versus
potential harms from false positives and overdiagnosis. Thus recommendations on the frequency of its
use are wide-ranging. Different
countries and professional societies have guidelines recommending from annual
to biennial to triennial or no screening at all.
In 2003, the American Cancer Society
(ACS) recommended annual mammography screening for all women starting at age 40
years and continuing as long as a woman remained in good health. The ACS also recommended clinical breast
examination (CBE) periodically for women in their 20s and 30s and annually for
women 40 years and older.
.
The ACS
has revised its guidelines regarding when and how often women at average risk should
receive screenings for breast cancer.
The ACS commissioned a systematic
evidence review in 2015 of the breast cancer screening literature and a
supplemental analysis of mammography registry data to address questions related
to the screening interval.
Formulation of recommendations was based on
the quality of the evidence and judgment about the balance of benefits and
harms such as biopsies resulting from false positive mammograms.
Screening mammography in women aged
40 to 69 years is associated with a reduction in breast cancer deaths to as
much as 30 percent, and inferential evidence supports breast cancer screening
for women 70 years and older that are in good health. Evidence does not support routine clinical
breast examination as a screening method for women at average risk.
Oeffinger et al review and analysis
are described in their paper in JAMA
and form the basis of the new ACS recommendations that are:
· - Women with an average risk of breast cancer should undergo
regular screening mammography starting at age 45 years (strong recommendation).
· - Women aged 45 to 54 years should be screened annually (qualified
recommendation).
· - Women 55 years and older should transition to biennial screening (strong recommendation).
· - Women should have the opportunity to begin annual screening
between the ages of 40 and 44 years (qualified recommendation).
· - Women should continue screening mammography as long as their
overall health is good and they have a life expectancy of 10 years or longer
(qualified recommendation).
The ACS does not recommend clinical breast examination for breast cancer screening among average-risk women at any age (qualified recommendation).
These updated ACS recommendations bring it closer to the
draft guidelines released on April 20, 2015, by the U.S. Preventive Services
Task Force (USPSTF) for breast cancer screening which are:
· For women at average risk for breast
cancer, most of the benefit of mammography will result from biennial screening
during ages 50 to 74 years.
· Of all age groups, women ages 60 to
69 years are most likely to avoid a breast cancer death through mammography
screening.
· Screening mammography in women ages
40 to 49 years may reduce the risk of dying of breast cancer, but the number of
deaths averted is much smaller than in older women and the number of
false-positive tests and unnecessary biopsies are larger.
· Women with a parent, sibling, or
child with breast cancer may benefit more than average-risk women from
beginning screening between the ages of 40 and 49 years.
· The USPSTF concludes that the current
evidence is insufficient to assess the balance of benefits and harms of
screening mammography in women age 75 years and older.
· The USPSTF concludes that the current
evidence is insufficient to assess the benefits and harms of tomosynthesis (3-D
mammography) as a screening modality for breast cancer.
The ACS and USPSTF guidelines are now more consistent and state that the decision to start screening
mammography prior to age 50 years should be an individual one. Both guidelines agree that for average-risk women younger than
45 years, the harms from false positive screening mammograms outweigh the
benefits. For women older than 55 years, biennial mammography is likely to
provide the most benefits while limiting the harms. The new ACS recommendation
to stop screening for older women with life expectancies of less than 10 years
is consistent with the emphasis on functional versus chronologic age. ACS is also recommending ending physical for
screening purposes by doctors entirely.
These recommendations do not apply to women age 40 years and older
who are at high risk because pre-existing breast cancer or a previously
diagnosed high-risk breast lesion and who are known to have underlying genetic
mutation (such as a BRCA mutation or other familial breast cancer syndrome) or
a history of chest radiation at a young age.
Women at high risk for developing breast cancer will require a more
personalized screening than the vast majority of women who are at average risk.
There will be many professional societies and well meaning doctors
who will disagree with the new guidelines from ACS and USPSTF but until and
when a well designed prospective randomized study provides findings that differ
with the above mentioned recommendations they will likely stand.
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