Friday, April 1, 2016

Decades long decline in Dementia

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

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


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.

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.
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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.