Cohort studyindependent cross-checkabstract checked I-SUP-107 standard review

Multivitamins and death in 390,000 Americans

Multivitamin Use and Mortality Risk in 3 Prospective US Cohorts.

Overview

Loftfield E et al.. JAMA Netw Open 2024 · PMID 38922615 · DOI 10.1001/jamanetworkopen.2024.18729

People who took multivitamins did not live longer; their risk of death was about 4% higher, which may reflect who takes supplements rather than the pills.

Does the study support the specific claim? Partly · Methodological quality: moderate

Original publication

Plain-language summary

Study explained simply
What did the researchers want to find out?

To see whether multivitamin users live longer.

How was the study done?

Three large cohort studies combined.

How many people, animals or samples were studied?

390,124 adults.

What was actually found?

No survival benefit; slight 4% higher death risk.

How large was the observed effect?

HR 1.04 (1.02-1.07).

What do the results mean in everyday life?

Multivitamins do not help healthy people live longer.

What are the study's limitations?

Observational; self-report.

What does it say about Elawady's specific claim?

Supports C-SUP-01; only weakly relevant to the harm claim in C-SUP-06.

Do the results apply to Germany and Europe?

Applicable.

What can explicitly not be concluded from this study?

Cannot prove that multivitamins cause harm.

Scientific in-depth review

1. Full reference

Authors
Loftfield E et al.
Journal
JAMA Netw Open
Year
2024
Identifier
PMID 38922615 DOI 10.1001/jamanetworkopen.2024.18729 · PMC11208972
Verification
verified – PubMed efetch 2026-10-26; Crossref works API 2026-10-26
Retracted
no
Corrections
none
Extent checked
abstract only
Conflicts of interest and funding

No COI statement in PubMed record; funding listed: Intramural NIH HHS

2. Research question

Is multivitamin use associated with mortality, accounting for healthy-user bias and reverse causation?

3. Study design and population

Study design
Cohort study – Pooled analysis of 3 prospective cohorts (NIH-AARP, PLCO, Agricultural Health Study)
Population

US adults without cancer or other chronic diseases at baseline

Country

USA

Period

Baseline 1993-2001; follow-up up to 27 years

Sample size

390,124 participants; 164,762 deaths

Inclusion and exclusion criteria

No history of cancer or other chronic diseases

4. Methods and endpoints

Exposure / intervention

Self-reported multivitamin use (baseline and follow-up)

Comparator

Non-users

Endpoints

All-cause and cause-specific mortality

Statistical methods

Multivariable Cox models; time-varying analyses

5. Actual results

Results

Daily MV use not associated with lower mortality: multivariable HR 1.04 (1.02-1.07) in the first half and 1.04 (0.99-1.08) in the second half of follow-up; similar HRs for major causes of death.

Absolute risks

not reported in abstract

Authors' conclusion

MV use was not associated with a mortality benefit.

6. Strengths

  • Very large
  • Long follow-up
  • Attention to healthy-user bias

7. Weaknesses

  • Observational; self-reported exposure
  • Residual confounding possible in either direction

8. Risk of bias

Orienting tool
ROBINS-E
Type of assessment
simplified assessment (abstract only)
Full formal assessment
no
Overall risk of bias
some concerns
Rationale

Observational exposure; confounding.

9. Assessment of the statistical interpretation

HR 1.04 is small; a slight excess could reflect reverse causation (ill people starting supplements); randomised data (COSMOS, PHS II) show no mortality effect.

10. Relevance to the specific claim

No mortality benefit of multivitamins in a very large cohort; the small positive HR resembles the Iowa signal but is much weaker.

11. Independent contrary findings

RCTs show no increase.

12. Transferability to Germany and Europe

Applicable.

13. Overall methodological judgement

Supports 'no benefit'; weak and non-causal evidence for 'harm'.

Multidimensional assessment
Multidimensional assessment
Authenticity of the sourceverified
Methodological qualitymoderate
Risk of biassome concerns
Precision of resultshigh
Directnessdirect
Reproducibilitypartly replicated
Consistency with the overall evidencemixed
Regional transferabilityhigh
Adequacy of the interpretation (by the archive)not applicable

14. Open questions

None material.

15. Linked fact checks