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. 2022 Jul 26:9:923981.
doi: 10.3389/fcvm.2022.923981. eCollection 2022.

Modification effect of changes in cardiometabolic traits in association between kidney stones and cardiovascular events

Affiliations

Modification effect of changes in cardiometabolic traits in association between kidney stones and cardiovascular events

Min Xu et al. Front Cardiovasc Med. .

Abstract

Backgrounds: Whether longitudinal changes in metabolic status influence the effect of kidney stones on cardiovascular disease (CVD) remains unclarified. We investigated the modification effect of status changes in metabolic syndrome (MetS) in the association of kidney stones with risk of incident CVD events.

Methods: We performed a prospective association and interaction study in a nationwide cohort including 129,172 participants aged ≥ 40 years without CVDs at baseline and followed up for an average of 3.8 years. Kidney stones information was collected by using a questionnaire and validated by medical records. The repeated biochemical measurements were performed to ascertain the metabolic status at both baseline and follow-up.

Results: 4,017 incident total CVDs, 1,413 coronary heart diseases (CHDs) and 2,682 strokes were documented and ascertained during follow-up. Kidney stones presence was significantly associated with 44%, 70% and 31% higher risk of CVDs, CHDs and stroke, respectively. The stratified analysis showed significant associations were found in the incident and sustained MetS patients, while no significant associations were found in the non-MetS at both baseline and follow-up subjects or the MetS remission ones, especially in women. For the change status of each single component of the MetS, though the trends were not always the same, the associations with CVD were consistently significant in those with sustained metabolic disorders, except for the sustained high blood glucose group, while the associations were consistently significant in those with incident metabolic disorders except for the incident blood pressure group. We also found a significant association of kidney stone and CVD or CHD risk in the remain normal glucose or triglycerides groups; while the associations were consistently significant in those with incident metabolic disorders except for the incident blood pressure group. We also found a significant association of kidney stone and CVD or CHD risk in the remain normal glucose or triglycerides groups.

Conclusions: A history of kidney stones in women with newly developed MetS or long-standing MetS associated with increased risk of CVD. The mechanisms link kidney stones and CVD risk in the metabolic and non-metabolic pathways were warranted for further studies.

Keywords: CVD; kidney stone; longitudinal change; metabolic disorders; modification effect.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Analysis of the hazard risk of kidney stones with risk of incident cardiovascular events by MetS x sex interaction subgroups. (A) Risk of cardiovascular diseases; (B) Risk of coronary heart disease; (C) Risk of stroke. Data are present as hazard ratio (HR) and 95% confidence interval (CI). P-values were calculated from the multivariable Cox regression models. Adjustments included for age (year), baseline level of body mass index (kg/m2), waist circumference (cm), quartiles of physical activity, quartiles of sedentary time, smoking status (current, former, and never), alcohol drinking (g/l), education level (percentage of high school and above), systolic and diastolic blood pressure (mmHg), fasting plasma glucose (mmol/l), oral glucose tolerance test 2-h glucose (mmol/l), HOMA-IR, low- and high-density lipoprotein cholesterol (mmol/l), and triglycerides (mmol/l), gall stone (yes or no), diet score and eGFR. MetS, metabolic syndrome.
Figure 2
Figure 2
Combined effect of kidney stones and MetS presence on risk of incident cardiovascular events by sex. (A) Women; (B) Men. P-values were calculated from the multivariable Cox regression models, after adjustments for the same covariates as Figure 1. MetS, metabolic syndrome.

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