Evidence map›Paper›PMID 35139112›Full record

ArticlePloS one2022

Why we should monitor disparities in old-age mortality with the modal age at death.

Viorela Diaconu, Alyson van Raalte, Pekka Martikainen

Abstract readHistorical Article
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. A Double Decomposition of Standard Deviation Below the Modal Age at Death and the Role of Causes of Death.European journal of population = Revue europeenne de demographie · 2026
    Article
  2. 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

3 authors.

Viorela DiaconuLifespan Inequalities Research Group, Max Planck Institute for Demographic Research, Rostock, Germany.ORCID 0000-0002-3098-4704
Alyson van RaalteLifespan Inequalities Research Group, Max Planck Institute for Demographic Research, Rostock, Germany.
Pekka MartikainenLifespan Inequalities Research Group, Max Planck Institute for Demographic Research, Rostock, Germany.ORCID 0000-0001-9374-1438

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Indicators based a fixed "old" age threshold have been widely used for assessing socioeconomic disparities in mortality at older ages. Interpretation of long-term trends and determinants of these indicators is challenging because mortality above a fixed age that in the past would have reflected old age deaths is today mixing premature and old-age mortality. We propose the modal (i.e., most frequent) age at death, M, an indicator increasingly recognized in aging research, but which has been infrequently used for monitoring mortality disparities at older ages. We use mortality and population exposure data by occupational class over the 1971-2017 period from Finnish register data. The modal age and life expectancy indicators are estimated from mortality rates smoothed with penalized B-splines. Over the 1971-2017 period, occupational class disparities in life expectancy at 65 and 75 widened while disparities in M remained relatively stable. The proportion of the group surviving to the modal age was constant across time and occupational class. In contrast, the proportion surviving to age 65 and 75 has roughly doubled since 1971 and showed strong occupational class differences. Increasing socioeconomic disparities in mortality based on fixed old age thresholds may be a feature of changing selection dynamics in a context of overall declining mortality. Unlike life expectancy at a selected fixed old age, M compares individuals with similar survival chances over time and across occupational classes. This property makes trends and differentials in M easier to interpret in countries where old-age survival has improved significantly.

Indexed as

Health Status DisparitiesMortalitySocioeconomic FactorsAdultAgedAged, 80 and overAge DistributionAge FactorsAgingCause of DeathData CollectionFemaleFinlandHistory, 20th CenturyHistory, 21st CenturyHumans

Identifiers

PMID35139112
PMCPMC8827466

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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.