Evidence map›Paper›PMID 39528775›Full record

ArticleArchives of osteoporosis2024

Total, dietary, and supplemental calcium intake and risk of all-cause, cardiovascular, and cancer mortality among U.S. adults: a prospective cohort study from the National Health and Nutrition Examination Survey.

Ran Chen, Ying Tang, Shunzheng Fang, Kai Gong, Dong Liu, Yu Xie, Guo Liu, Yu Tian, Lianyang Zhang, Yang Li and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Archives of osteoporosis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Ran Chen *War Trauma Medical Center, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical Center, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China.
Ying Tang *War Trauma Medical Center, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical Center, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China.
Shunzheng Fang *State Key Laboratory of Trauma, Burns and Combined Injury, Department of Rehabilitation Medicine, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China.
Kai GongDepartment of Orthopaedics, The First Affiliated Hospital of Chengdu Medical College, Chengdu, Sichuan Province, 610500, P.R. China.
Dong LiuWar Trauma Medical Center, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical Center, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China.
Yu XieWar Trauma Medical Center, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical Center, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China.
Guo LiuWar Trauma Medical Center, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical Center, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China.
Yu TianDepartment Of Wound Repair and Rehabilitation Medicine, Center of Bone Metabolism and Repair, State Key Laboratory of Trauma, Burns and Combined Injury, Trauma Center, Research Institute of Surgery, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China.
Lianyang ZhangWar Trauma Medical Center, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical Center, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China.
Yang LiWar Trauma Medical Center, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical Center, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China. liyang360@163.com.
Siru ZhouWar Trauma Medical Center, State Key Laboratory of Trauma, Burns and Combined Injury, Army Medical Center, Daping Hospital, Army Medical University, Chongqing, 400042, P.R. China. zhousiru1025@163.com.

Funding

Chongqing Acute and Critical Care Clinical Medical Research Center 3354181Health Commission of Sichuan Province 23LCYJ032Science & Technology Department of Sichuan Province 2021YFG0324
6 · The paper itself

Abstract

Calcium intake is widely recommended, but its association with mortality remains unclear. This study indicated higher levels of calcium intake were associated with lower mortality in American adults. However, a nonlinear association between calcium intake and mortality suggested that excessive calcium intake beyond a certain threshold may increase mortality risk. PURPOSE: The study aimed to investigate the association of total, dietary, or supplemental calcium intake with all-cause, cardiovascular, and cancer mortality in American adults.

methodsThis prospective cohort study used the National Health and Nutrition Examination Survey from 2005 to 2018. Participants were categorized into tertiles based on calcium intake. Risks of all-cause, cancer, or cardiovascular mortality and the dose-response relationship were estimated using weighted Cox proportional hazard regression and restricted cubic splines, with adjustments for demographic characteristics, comorbidities, laboratory parameters, and dietary data.

resultsIn total, 6172 participants were included (median age: 61 years), and 869 had died (CVD:217, cancer:224) during a median follow-up of 81 months. After adjusting for confounders, higher total calcium(≥ 1660mg/d) [HR, 95%CI: 0.867 (0.865-0.869)], dietary calcium(≥ 1075mg/d) [HR, 95%CI: 0.711 (0.709-0.713)], and supplemental calcium (≥ 600mg/d) [HR, 95%CI: 0.786 (0.784-0.787)] intake groups were associated with lower all-cause mortality risk compared to the lowest intake group. Similar beneficial associations were found for cardiovascular, cancer mortality, and across subgroups of various ages, genders, races and body mass indexes. In the dose-response analysis, a 'J-shaped' nonlinear relationship was observed between calcium intake and the risk of all-cause, cardiovascular, and cancer mortality.

conclusionsHigher levels of total, dietary, or supplemental calcium were associated with lower all-cause, cardiovascular, or cancer mortality. However, a nonlinear association between calcium intake and mortality suggested that excessive calcium intake beyond a certain threshold may increase mortality risk.

Indexed as

Calcium, DietaryCardiovascular DiseasesDietary SupplementsNeoplasmsNutrition SurveysAdultAgedCause of DeathFemaleHumansMaleMiddle AgedProspective StudiesRisk FactorsUnited StatesCalcium, DietaryAll-cause mortalityCalcium intakeCancer mortalityCVD mortalityNHANES

Identifiers

PMID39528775

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.