Evidence map›Paper›PMID 37264434›Full record

ArticleDiabetology & metabolic syndrome2023

Sexual dimorphism in mitochondrial dysfunction and diabetes mellitus: evidence from a population-based cohort study.

Shanjie Wang, JunChen Guo, Xiaoxuan Liu, Wei Tian, Yiying Zhang, Ye Wang, Yige Liu, Mingyan E, Shaohong Fang

Open access · goldAbstract read
In one paragraph

Article in Diabetology & metabolic syndrome, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Shanjie Wang *Department of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150000, China.
JunChen Guo *Department of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150000, China.
Xiaoxuan LiuDepartment of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150000, China.
Wei TianDepartment of Epidemiology and Biostatistics, School of Public Health, Jiamusi University, 154000, Jiamusi, China.
Yiying ZhangDepartment of Epidemiology and Biostatistics, School of Public Health, Harbin Medical University, Harbin, China.
Ye WangDepartment of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150000, China.
Yige LiuDepartment of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150000, China.
Mingyan EDepartment of Thoracic Radiotherapy, Harbin Medical University Cancer Hospital, Harbin, Nangang District, China. emingyan0996@163.com.
Shaohong FangDepartment of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, 150000, China. fangshaohong@hrbmu.edu.cn.
Harbin Medical University · CNMinistry of Education of the People's Republic of China · CNJiamusi University · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

Innovation project of Harbin Medical University 2022-KYYWF-0281National Natural Science Foundation of China 82072027National Natural Science Foundation of China 82170262National Natural Science Foundation of China 82200396
6 · The paper itself

Abstract

backgroundPathophysiological mechanisms underlying sex-based differences in diabetes remain poorly understood. Mitochondrial metabolite methylmalonic acid (MMA) accumulation reflects mitochondrial dysfunction which is involved in sex-specific pathophysiological responses biologically. We aimed to investigate the sex-specific associations between mortality risk and MMA in adults with the presence or absence of type 2 diabetes.

methodsThis cohort study included 24,164 adults (12,123 females and 12,041 males) from the NHANES study during 1999-2014. Both sexes were separately categorized as those with no diabetes, prediabetes, undiagnosed diabetes, and diagnosed diabetes. Circulating MMA level was measured at baseline by mass-spectrometric detection. Mortality status was ascertained from baseline until December 31, 2015.

resultsDuring a median follow-up of 11.1 years, 3375 deaths were documented. Males had a particularly higher mortality than females in adults with diagnosed diabetes compared to differences in those with no diabetes, prediabetes and undiagnosed diabetes (sex differences in mortality rate per 1000 person-years across diabetic status: 0.62, 1.44, 5.78, and 9.77, p < 0.001). Notably, the sex-specific difference in associations between MMA and mortality was significant only in adults with diagnosed diabetes (p for interaction = 0.028), not in adults with no diabetes and prediabetes. Adjusted HRs (95%CIs) per doubling of MMA for all-cause mortality were 1.19 (1.04-1.37) in females with diagnosed diabetes versus 1.58 (1.36-1.86) in male counterparts. In addition, MMA levels had an insignificant or weak correlation with sex hormone profiles at baseline, regardless of diabetes status and sex.

conclusionsSex difference in mortality risk was especially significant in diagnosed type 2 diabetes. Increasing equivalent exposure to mitochondrial metabolite MMA was associated with a greater excess risk of future mortality in males with diabetes than in females.

Indexed as

CardiometabolismCobalaminGender/SexMethylmalonic acidMitochondriaMortality

Identifiers

PMID37264434
PMCPMC10234037
OpenAlexW4379056561

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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.