Evidence map›Paper›PMID 42304222›Full record

ArticleBMC infectious diseases2026

Risk factors for community-acquired pneumonia in older adults in Japan after the introduction of the childhood PCV13.

Naoki Inoshima, Kei Nakashima, Kanzo Suzuki, Hirohiko Nagasaka, Toshiaki Niwa, Chikara Nakahama, Naoyuki Miyashita, Satomi Iwamoto, Sakae Kan, Kyoko Kondo and 2 more

Abstract readMulticenter Study
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Naoki Inoshima *Department of Pulmonology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, 296-8602, Chiba, Japan.
Kei Nakashima *Department of Pulmonology, Kameda Medical Center, 929 Higashi-cho, Kamogawa, 296-8602, Chiba, Japan. kei.7.nakashima@gmail.com.
Kanzo SuzukiDepartment of Community-based Medical Education, Nagoya City University Graduate School of Medical Sciences, Nagoya City University, Nagoya, Aichi, Japan.
Hirohiko NagasakaNagasaka Clinic, Okazaki, Aichi, Japan.
Toshiaki NiwaHamada Asai Clinic, Tajimi, Gifu, Japan.
Chikara NakahamaNakahama Clinic, Osaka, Osaka, Japan.
Naoyuki MiyashitaFirst Department of Internal Medicine, Division of Respiratory Medicine, Infectious Disease and Allergology, Kansai Medical University, Hirakata, Osaka, Japan.
Satomi IwamotoAsuke Hospital, Toyota, Aichi, Japan.
Sakae KanKaisei Hospital, Nagoya, Aichi, Japan.
Kyoko KondoOMU Core Facilities Life Sciences Section, Osaka Metropolitan University, Osaka, Osaka, Japan.
Satoko OhfujiDepartment of Public Health, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Osaka, Japan.
Wakaba FukushimaDepartment of Public Health, Graduate School of Medicine, Osaka Metropolitan University, Osaka, Osaka, Japan.

Funding

This study was supported by a grant for Research on Emerging and Re-emerging Infectious Diseases from the Ministry of Health, Labour and Welfare, Japan grant numbers: 20HA2001 and 24HA2007
6 · The paper itself

Abstract

backgroundCommunity-acquired pneumonia (CAP) remains a leading cause of death globally. Although childhood 13-valent pneumococcal conjugate vaccine (PCV13) has altered the epidemiology of pneumococcal disease in children, risk factors for CAP in older adults remain insufficiently explored. Additionally, few studies have compared risks between those aged 65-74 and ≥ 75 years. We evaluated risk factors for CAP in older Japanese adults by age.

methodsWe conducted a secondary analysis of data from a multicenter, nationwide case-control study conducted between October 2016 and December 2019. Cases were individuals aged ≥ 65 years with CAP. Up to five controls per case were matched by sex, fiscal-year age, and visit date. Clinical and lifestyle data were questionnaire-based. Adjusted odds ratios (aORs) were calculated for participants overall and stratified by age (65-74 and ≥ 75 years) using conditional logistic regression.

resultsAnalysis included 142 cases and 596 controls. CAP risk was associated with living with children ≤ 6 years (aOR: 6.15, 95% confidence interval [CI]: 2.84-13.32), low body mass index (BMI) (< 18.5 kg/m²) (aOR: 1.78, 95% CI: 1.02-3.09), and impaired activities of daily living (ADL) (aOR: 2.44, 95% CI: 1.12-5.30). High BMI (≥ 25.0 kg/m²) was associated with a reduced risk (aOR: 0.55, 95% CI: 0.31-0.95). Among those aged 65-74 years, living with children ≤ 6 years (aOR: 4.89, 95% CI: 1.83-13.08) was a risk factor for CAP, whereas high BMI (aOR: 0.41, 95% CI: 0.18-0.89) and gastrointestinal disease (aOR: 0.19, 95% CI: 0.04-0.84) were associated with a reduced risk. Among those aged ≥ 75 years, chronic obstructive pulmonary disease (aOR: 3.59, 95% CI: 1.29-9.93), asthma (aOR: 2.99, 95% CI: 1.25-7.16), living with children ≤ 6 years (aOR: 11.62, 95% CI: 3.12-43.33), and impaired ADL (aOR: 2.90, 95% CI: 1.10-7.65) were risk factors for CAP. Only living with children ≤ 6 years was significant for pneumococcal CAP (aOR: 7.22, 95% CI: 1.23-42.34).

conclusionsLiving with children ≤ 6 years remains a major CAP risk factor in older adults after childhood PCV13 introduction. However, risk factors differ by age. Respiratory comorbidities and functional decline are dominant drivers of CAP in adults aged ≥ 75 years. Prevention strategies should consider age-specific dominant risk factors.

Indexed as

Community-Acquired InfectionsCommunity-Acquired PneumoniaPneumococcal VaccinesPneumonia, PneumococcalAgedAged, 80 and overCase-Control StudiesFemaleHumansJapanMaleOdds RatioRisk Factors13-valent pneumococcal vaccinePneumococcal VaccinesCommunity-acquired pneumoniaOlder adultsRisk factors

Identifiers

PMID42304222
PMCPMC13505070

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.