Showing posts with label cardiovascular. Show all posts
Showing posts with label cardiovascular. Show all posts

Sunday, July 24, 2016

Global Sodium Consumption and Death from Cardiovascular Causes

INTRODUCTION
- A high dietary intake of Sodium is associated with elevated blood pressure, a major risk factor for cardiovascular disease.
- The United Nations (UN), World Health Organization (WHO), Centers for Disease Control and Prevention (CDC) and other organizations have emphasized the relationship between dietary sodium and cardiovascular outcomes.

- As part of the Global Burden of Diseases Nutrition and Chronic Diseases Expert Group
(NUTRICODE), we
i) Systematically identified and analyzed data on sodium consumption worldwide and calculated the dose-response effects of sodium on blood pressure in a new meta-analysis of trials.
ii) Compiled data to calculate the effects of blood pressure on cause-specific cardiovascular mortality and to characterize current blood-pressure levels and numbers of cause-specific deaths according to country, age, and sex
iii) Used data relating levels of sodium intake to blood pressure and cardiovascular events, as well as data on the lowest current levels of sodium intake according to country, to define a reference range for sodium consumption
iv) Used data (Table S1 in the Supplementary Appendix) to estimate the impact of current levels of sodium intake on cardiovascular mortality throughout the world

METHODS

Assessment of Global Sodium Consumption
- Search Period: March 2008 to December 2011
- Systematic searches were conducted for previously conducted national or subnational surveys on individual-level sodium consumption based on urinary excretion, estimated dietary intake, or both
- Data Included: 142 surveys with data from 24-hour urine collections and 91 with estimates of dietary intake, including 28 with both types of data (Table S2 in the Supplementary Appendix).
- These surveys included data from 66 countries, accounting for 74.1% of adults in the world.
- Using a hierarchical Bayesian model, we estimated the mean level of sodium consumption and statistical uncertainty according to age, sex, and calendar year in 187 nations.
- An article with detailed results of these analyses has been published previously (Powles et al. BMJ Open 2013; 3(12): e003733)

- Our model estimated sodium consumption with the use of 24-hour urine collections as the reference standard.
- To make our data comparable to data from prior regional surveys and blood pressure trials in which urinary sodium levels were measured, we did not adjust our analyses for sodium loss due to factors other than urinary excretion (e.g., sweat).

Effects of Reduced Sodium Intake on Blood Pressure
- Two recent Cochrane meta-analyses evaluated randomized trials of the effect of reduce sodium intake on blood pressure. (He et al. Cochrane Database Syst Rev
2013; 4: CD004937; Graudal et al. Cochrane Database Syst Rev 2011;11: CD004022)
- These meta-analyses did not determine whether blood-pressure lowering was linear across a range of sodium intakes and did not simultaneously quantify heterogeneity according to age, race, and the presence or absence of hypertension
- We performed a new meta-analysis evaluating all randomized interventions identified in these articles (Section S1 in Supplementary Appendix).
- Using data from these trials, we evaluated whether the effects of reduced sodium intake on blood pressure were linear.
- We evaluated the potential heterogeneity in this effect by taking into account population characteristics, including age, the presence or absence of hypertension, and race, as well as the duration of the intervention.
- We also assessed whether, apart from the presence or absence of hypertension, the effects of reduced sodium intake on blood-pressure lowering were blunted by the use of antihypertensive medication.

Effects of Blood-Pressure Levels on Cardiovascular Mortality
- To calculate the effects of systolic blood pressure on deaths from cardiovascular causes, we combined results from two large international projects (totaling 99 cohorts, 1.38 million participants, and 65,000 cardiovascular events) that pooled individual-level data, consistently adjusted for confounding.
- We accounted for regression dilution bias based on serial blood-pressure measures over time.
- We interpolated and extrapolated age-specific proportional effects (relative risks) of systolic blood pressure on cardiovascular mortality in 10-year age groups across the pooling projects (see Section S2 and Fig. S3 in the Supplementary Appendix).
- We used the same estimates of relative risk according to sex and race, on the basis of evidence of generally similar proportional effects of blood pressure on cardiovascular events according to sex and race in trials of antihypertensive drugs and observational studies of blood pressure and cardiovascular events.

Reference Levels of Sodium Consumption
- To define reference levels of sodium consumption, we conducted a search of published survey data, cohort studies, controlled trials, and dietary recommendations.
- We determined levels of sodium consumption that were associated with the lowest blood-pressure levels in ecologic studies and in randomized trials and with the lowest risk of disease in meta-analyses of prospective cohort studies
- We also considered at least theoretical feasibility based on the lowest national mean levels of consumption globally.
- Finally, we considered the consistency of our identified reference intake levels with major dietary guidelines.
- Details are provided in Section S4 in the Supplementary Appendix

Current Blood-Pressure Levels and Cause-Specific Mortality
- Data on current blood-pressure levels and cardiovascular mortality, each according to country, age, and sex, were compiled as part of the Global Burden of Disease Study 2010
- Data on blood pressure (from 786 country-years and 5.4 million participants) were obtained from published and unpublished health examination surveys and epidemiologic studies from around the world.
- Data on causes of death were obtained for 187 countries from 1980 through 2010; these data were obtained from vital-registration systems, verbal autopsies, mortality surveillance, census data, surveys, hospitals, police records, and mortuaries.
- Details of data collection and the statistical modeling used to estimate mean systolic blood pressure and causespecific mortality are provided in Table S1 and Sections S5 and S6 in the Supplementary Appendix

Cardiovascular Mortality Associated with Sodium Consumption above the Reference Level
- We estimated disease burdens using comparative risk assessment, capturing geographic and demographic variations in sodium intake, blood pressure, cardiovascular mortality, and corresponding uncertainties (details are provided in Table S1 and Section S7 in the Supplementary Appendix).
- We incorporated age-specific and sex-specific sodium intake, blood-pressure level, relative risk, and mortality data for each country to model the fraction and numbers of deaths estimated to be attributable to sodium intake above the reference level.

- The population-attributable fraction was estimated in a two-step process.
- First, we used the effects of sodium consumption on blood pressure according to age, the presence or absence of hypertension, and race to calculate the change in mean systolic blood pressure that would be expected from reducing sodium consumption to reference levels as defined above.
- Second, we used the age-specific effects of blood pressure on cardiovascular mortality to calculate the resulting change in risk.
- Estimated numbers of deaths attributable to sodium intake above the reference level were calculated by multiplying the population-attributable fraction by the absolute number of deaths in each country, age, and sex stratum.

RESULTS

Global Sodium Consumption
- We estimated that in 2010, the mean level of consumption of sodium worldwide was 3.95 g per day, and regional means ranged from 2.18 to 5.51 g per day (Fig. S1 in the Supplementary Appendix).
- Overall, 181 of 187 countries — 99.2% of the adult population in the world — had estimated mean levels of sodium intake exceeding the World Health Organization recommendation of 2.0 g per day, and 119 countries — 88.3% of the adult population in the world — exceeded this recommended level by more than 1.0 g per day.

Effects of Reduced Sodium Intake on Blood Pressure
- In our primary analysis of reduced sodium intake and blood pressure, we found strong evidence of a linear dose–response relationship (P < 0.001 for linearity and P = 0.58 for nonlinearity) (Fig. 1A).
- When the data were evaluated with the use of inverse-variance weighted meta-regression, each reduction of 2.30 g of sodium per day was associated with a reduction of 3.82 mm Hg (95% confidence interval [CI], 3.08 to 4.55) in blood pressure (Fig. 1B).


- The effects of dietary sodium on blood pressure were modified according to population characteristics, with larger reductions in blood pressure among (Fig. S2 in the Supplementary Appendix):
i) older persons >  younger persons
ii) blacks > whites,
iii) hypertensive > normotensive persons.
- For a white, normotensive population at 50 years of age, each reduction of 2.30 g per day in sodium intake lowered systolic blood pressure by 3.74 mm Hg (95% CI, 2.29 to 5.18).
- We did not find evidence of substantial blunting of the blood-pressure–lowering effects of sodium restriction by antihypertensive drugs, although the data available to address this question were limited. Further details are provided in Section S1 in the Supplementary Appendix

Effects of Blood Pressure on Cardiovascular Mortality
- The pooled analyses of blood pressure and cardiovascular mortality showed a log-linear (proportional) dose–response relationship, with no evidence of a threshold as low as a systolic blood pressure of at least 115 mm Hg (see Section S2 and Fig. S3 in the Supplementary Appendix).
- The relative magnitude of the effect on blood pressure decreased with age, in a manner similar to that seen with other cardiovascular risk factors.

Reference Levels of Sodium Consumption
- Potential reference levels of sodium consumption according to various definitions are shown in Table S3 in the Supplementary Appendix
- The lowest mean intake associated with both lower systolic blood pressure and a lower positive relationship between higher age and blood pressure in ecologic studies was 614 mg of sodium per day.
- In large, well-controlled, randomized feeding trials, the lowest tested sodium intake for which reductions in blood-pressure levels were clearly documented was 1500 mg per day.
- In prospective observational studies, the lowest mean sodium intake associated with a lower risk of cardiovascular events ranged from 1787 to 2391 mg per day.
- We also considered observed mean levels of sodium intake that have been associated with the lowest risk of stomach cancer (1245 mg per day).
- Levels of sodium intake associated with the lowest risk ranged from 614 to 2391 mg per day, depending on the type of evidence and the outcome.
- According to national data on sodium consumption, the estimated lowest observed mean national intake level was approximately 1500 mg per day.
- The maximum level of sodium intake recommended in major dietary guidelines ranged from 1200 to 2400 mg per day


Estimated Cardiovascular Mortality Attributed to Sodium Consumption
- On the basis of the correlations between sodium intake and blood pressure and between blood pressure and cardiovascular mortality that are described above, and using a reference level of sodium intake of 2.0±0.2 g per day, we found that 1.65 million deaths from cardiovascular causes (95% uncertainty interval, 1.10 million to 2.22 million) worldwide in 2010 were attributable to sodium consumption above the reference level (Table 1, and Table S4 in the Supplementary Appendix).

Of these deaths,
- 687,000 (41.7%) were due to coronary heart disease,
- 685,000 (41.6%) were due to stroke, and
- 276,000 (16.7%) were due to other cardiovascular disease.
- Globally, 40.4% of these deaths occurred prematurely (i.e., in persons younger than 70 years of age) (see Section S8 and Fig. S4 in the Supplementary Appendix).
- Four of every 5 sodium-associated deaths from cardiovascular causes (84.3%) occurred in low-income and middle-income countries.
- In sum, approximately 1 of every 10 deaths from cardiovascular causes worldwide (9.5%) (95% uncertainty interval, 6.4 to 12.8) and nearly 1 of every 5 (17.8%) premature deaths from cardiovascular causes were attributed to sodium consumption above the reference level.

- Across nine regions of the world, the absolute rate of sodium-associated deaths from cardiovascular causes was highest in Central Asia and Eastern and Central Europe (Fig. 2A, and Fig. S5 and Table S4 in the Supplementary Appendix).
- Proportional cardiovascular mortality was high in all regions: among younger adults, it exceeded 10% in nearly all regions and it exceeded 20% in Central Asia and Eastern and Central Europe, East Asia, and Southeast Asia (Fig. 2B).
- Among older adults, who have a higher absolute risk and more competing risk factors, proportional sodium-associated cardiovascular mortality approached or exceeded 10% in Central Asia and Eastern and Central Europe, East Asia, and Southeast Asia.
- Most sodium-associated cardiovascular deaths were due to coronary heart disease, except in East Asia, Southeast Asia, and sub-Saharan Africa, where most deaths from cardiovascular causes were due to stroke, especially hemorrhagic and other nonischemic strokes (Table S4 and Fig. S5 in the Supplementary Appendix). 


- Across individual nations, substantial variation was evident.
- Sodium-associated cardiovascular mortality was highest in the country of Georgia (1967 deaths per 1 million adults per year; 95% uncertainty interval, 1321 to 2647) and lowest in Kenya (4 deaths per 1 million adults per year; 95% uncertainty interval, 3 to 6) (Fig. 3).
- Proportional cardiovascular mortality ranged from 27.4% in Mauritius (95% uncertainty interval, 18.8 to 35.9) to 0.3% in Kenya (95% uncertainty interval, 0.2 to 0.4) (Fig. 4).


-Among the 30 most populous nations (Fig. S6 in the Supplementary Appendix), the highest sodium-associated cardiovascular mortality was in Ukraine (1540 deaths per 1 million adults per year; 95% uncertainty interval, 1017 to 2099), and the highest proportional mortality was in China (15.3% of all cardiovascular deaths; 95% uncertainty interval, 10.5 to 20.2).
- Detailed information about individual nations is provided in Section S9 and Table S5 in the Supplementary Appendix.

- In sensitivity analyses, lowering the definition of the reference intake level from 2.0 to 1.0 g of sodium per day increased the number of deaths from cardiovascular causes in the world that were attributed to sodium consumption by approximately 40%, to 2.30 million (95% uncertainty interval, 1.55 million to 3.07 million) (Tables S6 and S7 and Fig. S7 and S8 in the Supplementary Appendix).
- When we estimated effects attributable only to sodium intake above 4.0±0.4 g per day, 512,901 worldwide deaths from cardiovascular causes (95% uncertainty interval, 333,710 to 704,773) were attributed to such consumption (Tables S8 and S9 in the Supplementary Appendix).
- This was the estimated number of deaths that were potentially preventable if only the nations with the highest level of sodium consumption lowered their intake to just the current mean intake in the world.
- If we altered our model so that the estimated benefits of blood-pressure lowering did not continue below 125 mm Hg, 1.55 million deaths from cardiovascular causes in the world (95% uncertainty interval, 1.10 million to 2.10 million) were attributed to sodium consumption above a level of 2.0 g per day.

DISCUSSION

Main Findings
- Globally, 1.65 million deaths from cardiovascular causes in 2010 — about 1 of 10 deaths from cardiovascular causes — were attributed to sodium consumption of more than 2.0 g per day.
- Notably, 4 of 5 of these deaths occurred in low and middle-income countries, and 2 of 5 of these deaths occurred prematurely (before the age of 70 years).

Regional Findings
- Our findings also show and quantify the heterogeneity in disease burden attributed to sodium according to region, age, and type of cardiovascular disease.
- Yet, we also found that no region and few countries were spared.
- Whereas estimated sodium-associated cardiovascular mortality was highest in Central Asia, it was high (more than 750 deaths per 1 million adults who were 70 years of age or older) in all regions.
- The estimated number of proportional sodium-associated deaths was also high, approaching or exceeding 15% of premature deaths from cardiovascular causes in most regions

Dose-response relationship between sodium intake and blood pressure
- Our meta-analysis of 107 randomized interventions in 103 trials showed a linear dose–response relationship between reduced sodium intake and blood pressure, jointly modified according to age, race, and the presence or absence of hypertension.
- These findings are consistent with the findings of a meta-analysis, published after submission of this article, that included fewer trials (34 trials).
- Larger effects in older adults and hypertensive persons would be consistent with decreasing vascular compliance and renal filtration; in blacks, larger effects would be consistent with differences in renal handling of sodium.
- We used randomized trials of reduced sodium intake and blood pressure to estimate the more conceptually appropriate effect of lifetime differences in intake, because direct evidence on lifetime effects, which may be larger, is available only from ecologic comparisons and experiments involving nonhuman primates

Possible controversy
- Some researchers have argued that it may not be possible to directly extrapolate the effects of sodium on blood pressure to cardiovascular risk.
- However, the effect on cardiovascular disease is supported by extensive experimental and ecologic evidence, data on cardiovascular events from some trials of reduced sodium intake, and evidence of the cardiovascular benefits of blood-pressure lowering across multiple interventions (see Section S3 in the Supplementary Appendix).
- A meta-analysis of prospective cohort studies showed that higher sodium consumption was associated with a higher rate of death from coronary heart disease (relative risk, 1.32; 95% CI, 1.13 to 1.53) and death from stroke (relative risk, 1.63; 95% CI, 1.27 to 2.10), the two main end points in our analysis.
- Although concerns have been raised that reduced sodium intake may cause physiological harm, a meta-analysis of 37 trials showed no significant adverse effects on blood lipid levels, catecholamine levels, or renal function

Results from observational studies
- There is mixed evidence from observational data on the relationship between very low sodium intake and cardiovascular events.
- A recent Institute of Medicine report concluded that, if restricted to studies of clinical cardiovascular events, there is insufficient evidence that lowering sodium intake further beyond 2.30 g per day either increases or decreases the occurrence of cardiovascular disease.
- Yet the report further concluded that the entirety of the evidence, “when considered collectively, indicates a positive relationship between higher levels of sodium intake and [the] risk of cardiovascular disease.”
- Although precise targets for sodium reduction remain controversial, various organizations tasked with reviewing all the evidence have arrived at target levels ranging from 1200 to 2400 mg per day (Table S3 in the Supplementary Appendix).

Limitations
- Causality cannot be proved, although every effort was made to maximize validity, minimize error and bias, and incorporate heterogeneity and uncertainty,
- Dietary sodium was estimated based on 24-hour urine collections, which reflect approximately 90% of intake and also can be limited by incomplete collection.
- Data on sodium intake were not available across all countries or years - increased statistical uncertainty and the risk that some data could reflect sampling bias.
- Dietary sodium is also associated with nonfatal cardiovascular disease, kidney disease, and gastric cancer, the second-leading fatal cancer worldwide – may underestimate the full global health effects of dietary sodium.
- No data on potassium consumption – also influences blood pressure and the risk of stroke.
- Specific approaches or timelines for reduced sodium intake was not incorporated.

CONCLUSION
- On the basis of currently available data on sodium consumption, dose–response effects on blood pressure and cardiovascular mortality, and cause-specific deaths, we estimate that in 2010, a total of 1.65 million deaths from cardiovascular causes were attributable to consumption of more than 2.0 g of sodium per day.



Correspondence (Comment by other experts and the authors' reply)

Thursday, July 7, 2016

Breast Milk Consumption in Preterm Neonates and Cardiac Shape in Adulthood

Introduction
- Preterm birth relates to long-term alteration in cardiac morphology and function
- We hypothesized that fed human breast milk during early postnatal life is beneficial to long-term cardiac structure and function in preterm-born individuals compared with infant formulas.

Methods
-926 preterm-born infants originally took part in RCT of postnatal milk-feeding regimes between 1982 and 1985 across 5 different UK centres.
- These individuals had birth weight of <1850g and had no major congenital anomalies
- They were randomly assigned to either breast milk donated by unrelated lactating women or nutrient-enriched formulas.
- 102 individuals from this cohort were followed: 30 were fed exclusively human milk (EHM) and 16 were fed exclusively formula (EFF)
- Comparison group: 102 individual born term to uncomplicated pregnancies with age and sex distribution similar to those of the preterm-born young adults
- Cardiac morphology and function were assessed by MRI (1.5-T Siemens Sonata scanner)
- All data were coded with subject- and study-specific IDs to ensure anonymity and blinded analysis

Results
- No significant differences in both groups in perinatal characteristics or anthropometrics, demographics, blood biochemistry, or blood pressure in young adulthood (Table 1)
- However, both groups had altered blood biochemistry profiles and increased blood pressures compared with young adults born term
- There were no significant differences in number of smokers, personal and family medical history, or lifestyle factors, such as socioeconomic status, physical activity, or diet (P > .05) between the 2 milk-feeding preterm groups, nor with control group.



Left and Right Ventricular Size and Function
Compared with preterm-born individuals who were exclusively formula fed as infants, preterm-born individuals fed exclusively human milk as infants had:
- Increased left and right ventricular end-diastolic volume index (+9.73%, P = .04 and +18.2%, P < .001) and
- Increased left and right stroke volume index (+9.79%, P = .05 and +22.1%, P = .01)

- Although both feeding groups still had significantly smaller left ventricular end-diastolic volume index and stroke volume index than adults born term, the reduction in the group fed EHM was only ∼9% compared with 18% in the group fed EFF for both left ventricular end diastolic volume index and stroke volume index.

- Both preterm-born groups had similar left ventricular mass index and ejection fraction, although the preterm group fed EFF had significantly shorter left ventricles with reduced left ventricular luminal diameters.
- Right ventricular mass index and length were similar between preterm groups (Table 2). However, preterm-born young adults fed EHM had similar right ventricular ejection fractions as term-born young adults, whereas preterm-born young adults fed EFF showed reduced right ventricular ejection fractions compared with term-born controls.

Left Ventricular Shape and Native T1 Imaging
- Shape analysis confirmed the differences in size observed by using standard metrics (Fig 3), which particularly highlighted the significant increase in left ventricular length (P < .001) in the EHM group compared with the preterm individuals fed EFF
- Importantly, there were no other major geometric variations identified between preterm-born individuals fed EHM and those fed EFF (Fig 3) or term-born adults.
- We did not observe significant differences in myocardial tissue characterization by T1 mapping


Predictors of Cardiac Changes
- In multivariable models including gestational age, sex, postnatal milkfeeding group, and postnatal weight gain, gestational age remained an independent predictor for all 4 cardiac measures (P < .001); however, being fed EHM was also an independent predictor of left ventricular end-diastolic volume index (P = .007), left ventricular stroke volume index (P = .03), right ventricular end-diastolic volume index (P = .002), and right ventricular stroke volume index (P = .004).
- In line with the changes between preterm feeding groups being greater for the right ventricle, in a multivariable regression model across the entire preterm group (n = 102) with gestational age, sex, percentage of human milk in the diet, and postnatal weight gain as the predictors, the percentage of human milk was positively related to both right ventricular end-diastolic volume index (P = .009) and stroke volume index (P = .04), but not left ventricular parameters.
- There were no correlations between percentage of expressed milk and cardiac measures within the group fed EHM.

Thoracic Cavity Size and Pulmonary Artery Diameters
- Preterm-born young adults fed EFF had reduced thoracic cavity dimensions compared with those fed EHM
- No difference in aortic diameters
- EFF groups had increased main pulmonary artery diameters and pulmonary artery to aortic diameter ratios. Pulmonary artery to aortic diameter ratios were inversely related to right ventricular end-diastolic volume index and stroke volume index but not left ventricular parameters.

Discussion
- Breast milk contains a greater bioactivity and bioavailability of a number of growth factors, enzymes, and antibodies compared with even the best infant formulas. These factors are relevant to normal growth and development, as well as improving preterm infant health
- The data suggest that breast milk may reduce the risk of pulmonary arterial hypertension and future cardiopulmonary disease in preterm-born individuals
- These findings suggest the changes in cardiac morphology observed in preterm-born individuals relate primarily to size rather than geometric alterations, and that breast milk leads to proportional normalization of size.
- support the necessity of breast milk as part of early nutrition for individuals born to pregnancy complications as a protective mechanism to cardiovascular development
  
- Although our data suggest that it is not possible to reverse all cardiac changes related to the degree of prematurity through breast milk feeding, the magnitude of the differences between preterm-born adults fed EHM and those fed EFF is substantial and occurs independent of gestational age.
- Our finding that percentage of human milk consumed was positively associated with right ventricular morphology and function suggests that even small amounts of human milk in the preterm postnatal diet may be beneficial

Limitation
- This study does not prove causality
- Number of participants were relatively small compared with the size of the original cohort
- This study was not fully randomized, and as such, there is risk of ascertainment bias.

Strength
- Our preterm groups were similar in baseline demographics and demographic characteristics in young adulthood
- Unlike other studies that often rely on questionnaires and recall, we can be certain of the exact dietary intake of our preterm-born individuals during early postnatal life
  
Conclusion
- This is the first evidence of a beneficial association between breast milk and cardiac morphology and function in adult life for those born preterm
- Support promotion of human milk for the care of preterm infants to reduce long-term cardiovascular risk

Thursday, June 23, 2016

Body-Mass Index in 2.3 Million Adolescents and Cardiovascular Death in Adulthood

AIM
- To investigate the association between body mass index (BMI) in late adolescence and death from cardiovascular disease in adulthood.

METHOD
-BMI data from 1967 through 2010 Israeli adolescents (mean age 17.3±0.4 years) were grouped according to age- and sex- specific percentiles from the US CDC.
[Underweight: <5th percentile
Normal weight: 5th to 24th percentile (Reference group), 25th to 49th percentile, 50th to 74th percentile, 75th to 85th percentile
Overweight: 85th to 94th percentile
Obese: ≥ 95th percentile]
- Total number of study sample: 2,298,130 participants
- Primary outcomes: number of deaths attributed to coronary heart disease, stroke, sudden death from unknown cause or a combination of all three categories (total cardiovascular causes) by mid-2011.
- Statistical analysis: Cox proportional-hazards models; imputed 1.4% of missing values (country of origin, education and socioeconomic status) using multiple imputation algorithm; applied linear and quadratic terms using the midpoint of each BMI percentile group or the median of each absolute BMI group; spline models were fit to estimate the BMI value associated with minimum cardiovascular mortality and the lowest BMI associated with significantly increased mortality.

RESULTS
- During 42,297,007 person-years of follow-up, 2918 of 32,127 deaths (9.1%) were from cardiovascular causes, including 1497 from coronary heart disease, 528 from stroke, and 893 from sudden death.
- The mean ages at the time of death were 47.4 years for coronary heart disease, 46.0 years for stroke, and 41.3 years for sudden death
- The rates of death per person-year were generally lowest in the group that had BMI values during adolescence in the 25th to 49th percentiles, with higher rates observed among those below the 5th percentile.
- A graded increase in the risk of death from cardiovascular causes and all causes that started among participants in the group that was in the 50th to 74th percentiles of BMI (i.e., within the accepted normal range).

Analysis based on percentile grouping
Hazard ratio after multivariable adjustment* (Reference group: 5th to 24th percentile):
- Overweight (85th to 94th percentiles): 3.0 (95% CI, 2.5-3.7) for death from coronary heart disease, 1.8 (95% CI, 1.3-2.5) for death from stroke, 1.5 (95% CI, 1.1-1.9) for sudden death, and 2.2 (95% CI, 1.9-2.6) for death from total cardiovascular causes
-Obese group (≥95th percentile for BMI): 4.9 (95% CI, 3.9-6.1) for death from coronary heart disease, 2.6 (95% CI, 1.7-4.1) for death from stroke, 2.1 (95% CI, 1.5-2.9) for sudden death and 3.5 (9.5% CI, 2.9-4.1) for death from total cardiovascular causes
*(adjustment for sex, age, birth year, sociodemographic characteristics, and height)

Analysis based on year of follow-up
- Hazard ratio from death from cardiovascular disease increased from 2.0 (95% CI 1.1 to 3.9) during follow-up for 0 to 10 years to 4.1 (95% CI 3.1 to 5.4) during follow-up for for 30 to 40 years
- The risk was persistently high for death from coronary heart disease across the entire period of follow-up.

Analysis of absolute values of BMI
- Participants with a BMI ranging from 20.0 to 22.4 had a higher risk of death from coronary heart disease than did those with a BMI ranging from 17.5 to 19.9 (hazard ratio, 1.2; 95% CI, 1.1-1.4)
- The risks of death from stroke, sudden death, and total cardiovascular causes (along with noncardiovascular causes and all causes) were also elevated starting with a BMI of 22.5 and increased more steeply among the extremely obese for cardiovascular-specific death
On multivariable-adjusted spline models,
-The minimum risks of death from stroke, sudden death, and cardiovascular causes were among participants who had BMI values of 19.8, 19.3, and 18.3, respectively, whereas the association with death from coronary artery disease was graded across the full range of BMI-percentile groups
- Participants had a significantly elevated risk of death from total cardiovascular causes starting at BMI values above 20.3.

Analysis by z-scores of BMI
- After multivariable adjustment, the hazard ratios for death from coronary heart disease were 1.54 (95% CI, 1.46 to 1.62) for men and 1.58 (95% CI, 1.31 to 1.91) for women per 1-unit increment in the z score

Sensitivity analysis
- Findings persisted in extensive sensitivity analyses: sex-specific, restricted to adolescents with unimpaired health status, analysis modelling the association without competing risks that used the group with BMI values in the 25th to 49th percentiles as the reference category, restricted to participants who were evaluated after 1981 and to those who were evaluated from 1967 through 1980, comparing deaths that occurred before the age of 45 years with those that occurred at the age of 45 years or older, analyses according to calendar periods of follow-up and country of origin, and an analysis that included all cardiovascular diseases defined according to ICD coding (9.9% of all deaths)

Analysis of population-attributable fractions
- Among participants with a BMI higher than the 50th percentile in 2013, the projected population-attributable fractions were 28% for death from total cardiovascular causes and 36% for death from coronary heart disease

DISCUSSION
- There is a graded increase in the risk of death starting at the mid-normal range of adolescent BMI (50th to 74th percentiles) and that the high normal BMI range (75th to 84th percentiles) was associated with hazard ratios of 2.2 for coronary heart disease and 1.8 for total cardiovascular causes.
- Our findings appear to provide a link between the secular trends in adolescent overweight and coronary mortality during the past decades. In contrast to the steep decline in the rate of death from cardiovascular causes among older age groups, cardiovascular mortality among young adults has not decreased or the decline has slowed in several developed countries.

LIMITATIONS
- Absence of adult measures of BMI, an independent effect of adolescent BMI on death from cardiovascular disease in adulthood cannot be assessed.
- Unable to account for important cardiovascular lifestyle risk factors (such as smoking, exercise, and physical fitness) that may confound the BMI association, although adjustment for smoking had no effect in other studies, and a mendelian randomization study showed effects for BMI that were independent of confounding
- The study sample is less representative of Israeli women, and the findings need to be confirmed in a racially and ethnically diverse population

CONCLUSION
- An increased BMI in late adolescence, even within the currently accepted normal range, was strongly associated with cardiovascular mortality in young adulthood or midlife
- We could not determine whether an increased BMI in adolescence is an independent risk factor, is mediated by adult obesity, or both