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Acute coronary syndrome without documented standard modifiable risk factors and the stress hyperglycaemia ratio in an Indonesian percutaneous coronary intervention registry Cover

Acute coronary syndrome without documented standard modifiable risk factors and the stress hyperglycaemia ratio in an Indonesian percutaneous coronary intervention registry

Open Access
|Nov 2026
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Figures & tables

Figure 1-

Study flow. Derivation of the analysis cohort from the institutional PCI registry and allocation to the analytical objectives. SMuRF status was taken from the documented history at the index admission; all four-history fields were populated in every record. All 204 patients without a documented SMuRF were admitted between April 2026 and July 2026. The glycaemic analyses use the analytic cohort defined after the recording-bound audit. ACS, acute coronary syndrome; PCI, percutaneous coronary intervention; SMuRFs, standard modifiable cardiovascular risk factors.

Table 1-

Data-quality audit: number of records at the lower and upper recording bounds of each continuous variable (n = 1702).

VariableLower boundn (%) at boundMean of 5 adjacent valuesUpper boundn (%) at boundMean of 5 adjacent values
HbA1c (%)4182 (10.7)14.01526 (1.5)2.0
Total cholesterol (mg/dL)60150 (8.8)3.24506 (0.4)1.0
LDL cholesterol (mg/dL)2094 (5.5)3.23504 (0.2)1.2
Creatinine (mg/dL)0.345 (2.6)7.61521 (1.2)1.0
eGFR (mL/min/1.73 m2)331 (1.8)1.215023 (1.4)1.0
GRACE score4073 (4.3)4.23203 (0.2)1.0
Heart rate (beats/min)3054 (3.2)7.61805 (0.3)1.4
BMI (kg/m2)1432 (1.9)2.247.71 (0.1)1.0
Registry glucose (mg/dL)711 (0.1)1.280013 (0.8)1.0
Systolic blood pressure (mmHg)701 (0.1)1.22371 (0.1)2.0
LV ejection fraction (%)201 (0.1)5.8741 (0.1)4.0

[i] BMI, body mass index; eFGR, estimated glomerular filtration rate; LDL, low-density lipoprotein; LV, left ventricular; SMuRF, standard modifiable cardiovascular risk factor.

Figure 2-

Data-quality audit. (A) Distribution of recorded HbA1c, with values at the lower (4.0%) and upper (15.0%) recording bounds highlighted. (B) Distribution of the SHR in the analytic cohort and in the excluded boundary-HbA1c records, showing the inflation produced by a truncated denominator. (C) Number of records at the lower recording bound of eight variables compared with the mean number at the five adjacent values. BMI, body mass index; eFGR, estimated glomerular filtration rate; SHR, stress hyperglycaemia ratio; SMuRF, standard modifiable cardiovascular risk factor.

Figure 3-

ACS without a documented SMuRF. (A) Proportion by age group with Wilson 95% CIs; the number of patients without a documented SMuRF and the group size are shown in each bar. (B) ORs comparing patients without and with a documented SMuRF, adjusted for age and sex (the in-hospital death model is Firth-penalised and additionally adjusted for STEMI). Red markers denote intervals excluding 1. Multivessel PCI is defined as two or more vessels treated. ACS, acute coronary syndrome; CI, confidence intervals; LAD, left anterior descending artery; OR, odds ratio; PCI, percutaneous coronary intervention; SMuRFs, standard modifiable cardiovascular risk factors; STEMI, ST-elevation myocardial infarction.

Table 2-

Proportion of patients without a documented SMuRF under the primary and five pre-specified alternative definitions (n = 1702).

Definitionn/NProportion, % (95% CI)
Primary definition (no documented history of any of the four SMuRFs)204/170212.0 (10.5–13.6)
Hypercholesterolaemia broadened to history or LDL-C ≥130 mg/dL172/170210.1 (8.8–11.6)
Diabetes broadened to history or HbA1c ≥6.5%204/170212.0 (10.5–13.6)
Hypertension broadened to history or admission SBP ≥140 mmHga160/17029.4 (8.1–10.9)
Ever-smoking substituted for current smoking64/17023.8 (3.0–4.8)
All four broadenings applied together45/17022.6 (2.0–3.5)

ACS, acute coronary syndrome; CIs, confidence intervals; SMuRFs, standard modifiable cardiovascular risk factors. Wilson CIs. Broadened definitions add measured values from the index admission to the documented history.

a Admission blood pressure during ACS is not evidence of chronic hypertension; this definition tests sensitivity to under-ascertainment only. All patients without a documented SMuRF were admitted between April 2026 and July 2026 (0/1473 before April 2026; 204/229 from April 2026).

Table 3-

Baseline characteristics, presentation, markers of index-event severity and in-hospital death of patients with ACS, by documented SMuRF status.

VariablenOverall≥1 SMuRFNo documented SMuRFp
Demographics and medical history (not part of the SMuRF definition)
Age (years)170260 (52–66)60 (52–66)62 (55–69)<0.001
Male sex17021266 (74.4)1123 (75.0)143 (70.1)0.159
BMI (kg/m2)170224.5 (21.2–28.3)24.9 (21.0–28.8)23.4 (21.7–25.6)<0.001
Ever smoking17021258 (73.9)1118 (74.6)140 (68.6)0.081
Family history of premature CVD1702242 (14.2)209 (14.0)33 (16.2)0.455
Previous myocardial infarction170243 (2.5)38 (2.5)5 (2.5)1.000
Previous PCI1702181 (10.6)156 (10.4)25 (12.3)0.497
Previous heart failure1702294 (17.3)253 (16.9)41 (20.1)0.299
Cerebrovascular disease170234 (2.0)33 (2.2)1 (0.5)0.114
Chronic kidney disease170231 (1.8)28 (1.9)3 (1.5)1.000
Documented SMuRFs (defining variables)
Hypertension17021093 (64.2)1093 (73.0)0 (0.0)<0.001
Diabetes mellitus17021013 (59.5)1013 (67.6)0 (0.0)<0.001
Dyslipidaemia1702946 (55.6)946 (63.2)0 (0.0)<0.001
Current smoking1702710 (41.7)710 (47.4)0 (0.0)<0.001
Measurements linked to the SMuRF definition (differences expected by construction)
Systolic blood pressure (mmHg)1702140 (125–158)143 (128–160)125 (112–137)<0.001
Diastolic blood pressure (mmHg)170289 (81–99)90 (83–100)76 (68–84)<0.001
Total cholesterol (mg/dL)1702162 (110–218)168 (112–224)142 (106–173)<0.001
LDL cholesterol (mg/dL)1702116 (71–165)124 (76–171)80 (60–110)<0.001
HbA1c (%)a14947.2 (5.8–9.1)7.7 (6.1–9.5)5.9 (5.5–6.0)<0.001
Registry glucose (mg/dL)a1494187 (145–289)204 (151–310)150 (126–170)<0.001
Other measurements
SHRa14941.29 (0.98–1.69)1.30 (0.94–1.79)1.27 (1.13–1.43)0.731
Heart rate (beats/min)170282 (63–100)82 (63–102)80 (66–93)0.067
Creatinine (mg/dL)17021.1 (0.8–1.4)1.1 (0.8–1.4)1.0 (0.8–1.3)0.577
eGFR (mL/min/1.73 m2)170278 (54–99)78 (54–99)75 (53–96)0.467
GRACE risk score1702134 (95–173)136 (96–176)126 (95–156)0.035
Presentation and markers of index-event severity
STEMI presentation1702941 (55.3)840 (56.1)101 (49.5)0.090
Myocardial infarction (STEMI or NSTEMI)17021382 (81.2)1229 (82.0)153 (75.0)0.020
Killip class III–IV1702366 (21.5)318 (21.2)48 (23.5)0.509
Killip class II–IV1702681 (40.0)599 (40.0)82 (40.2)1.000
LV ejection fraction (%)170252 (48–56)52 (48–56)52 (48–56)0.978
LV ejection fraction <40%1702371 (21.8)322 (21.5)49 (24.0)0.466
Procedure
Vessels treated, n17022 (1–3)2 (1–3)1 (1–3)0.002
LAD treated17021144 (67.2)1025 (68.4)119 (58.3)0.005
Left main treated170282 (4.8)72 (4.8)10 (4.9)1.000
Multivessel PCI (≥2 vessels treated)b17021102 (64.7)1004 (67.0)98 (48.0)<0.001
Registry ‘multivessel’ fieldb17021198 (70.4)1079 (72.0)119 (58.3)<0.001
Radial access1702250 (14.7)211 (14.1)39 (19.1)0.072
Discharge medication and in-hospital outcome
Statin at dischargec16491647 (99.9)1449 (99.9)198 (100.0)1.000
P2Y12 inhibitor at dischargec16491641 (99.5)1443 (99.4)198 (100.0)0.607
Aspirin at dischargec16491629 (98.8)1432 (98.7)197 (99.5)0.499
In-hospital all-cause death170253 (3.1)47 (3.1)6 (2.9)1.000

ACS, acute coronary syndrome; CVD, cardiovascular disease; eGFR, estimated glomerular filtration rate; IQR, interquartile range; LAD, left anterior descending artery; LDL, low-density lipoprotein; LV, left ventricular; NSTEMI, non-ST-elevation myocardial infarction, PCI, percutaneous coronary intervention; SMuRF, standard modifiable cardiovascular risk factor; STEMI, ST-elevation myocardial infarction.

Continuous variables are median (IQR); categorical variables are n (%). The n column gives the number of records contributing to that row.

a Calculated in the analytic cohort of 1494 patients (≥1 SMuRF n = 1290; no documented SMuRF n = 204) after exclusion of boundary-recorded HbA1c; all other rows use all 1702 records (≥1 SMuRF n = 1498; no documented SMuRF n = 204).

b Multivessel PCI is derived from the number of vessels treated; the registry ‘multivessel’ field disagreed with this count in 356 records and is shown for transparency.

c Missing only for the 53 in-hospital deaths. All patients without a documented SMuRF were admitted between April 2026 and July 2026.

Table 4-

Adjusted differences between patients without and with a documented SMuRF.

CharacteristicEffect measureEstimate (95% CI)pn
Measurements linked to the SMuRF definition (differences expected by construction)
Systolic blood pressure (mmHg)Adjusted mean difference−20.18 (−23.62 to −16.74)<0.0011702
Diastolic blood pressure (mmHg)Adjusted mean difference−15.69 (−17.65 to −13.74)<0.0011702
Total cholesterol (mg/dL)Adjusted mean difference−35.43 (−46.87 to −23.99)<0.0011702
LDL cholesterol (mg/dL)Adjusted mean difference−38.25 (−47.55 to −28.94)<0.0011702
HbA1c (%)aAdjusted mean difference−2.23 (−2.57 to −1.90)<0.0011494
Registry glucose (mg/dL)aAdjusted mean difference−98.55 (−118.63 to −78.47)<0.0011494
Variables not part of the SMuRF definition
Age (years)Adjusted mean difference+3.29 (1.81–4.78)<0.0011702
BMI (kg/m2)Adjusted mean difference−1.55 (−2.39 to −0.70)<0.0011702
Heart rate (beats/min)Adjusted mean difference−4.89 (−9.12 to −0.66)0.0231702
Creatinine (mg/dL)Adjusted mean difference−0.38 (−0.67 to −0.10)0.0091702
eGFR (mL/min/1.73 m2)Adjusted mean difference+3.69 (−0.53 to 7.92)0.0871702
GRACE risk scoreAdjusted mean difference−18.66 (−25.46 to −11.87)<0.0011702
SHR (mean)a,bAdjusted mean difference−0.17 (−0.28 to −0.06)0.0031494
LV ejection fraction (%)Adjusted mean difference−0.31 (−1.93 to 1.30)0.7051702
Vessels treated, nAdjusted mean difference−0.21 (−0.38 to −0.04)0.0171702
STEMI presentationaOR0.77 (0.57–1.03)0.0751702
Myocardial infarction versus unstable anginaaOR0.65 (0.46–0.91)0.0141702
Killip class III–IVaOR1.13 (0.80–1.60)0.4891702
Killip class II–IVaOR1.01 (0.75–1.36)0.9461702
LV ejection fraction <40%aOR1.14 (0.81–1.62)0.4501702
LAD treatedaOR0.64 (0.48–0.87)0.0041702
Left main treatedaOR1.12 (0.57–2.22)0.7451702
Multivessel PCI (≥2 vessels treated)aOR0.46 (0.34–0.62)<0.0011702
Radial accessaOR1.48 (1.01–2.17)0.0441702
In-hospital all-cause deathaOR (Firth)0.82 (0.32–1.78)0.6371702

aOR, adjusted odds ratio; eFGR, estimated glomerular filtration rate; LAD, left anterior descending artery; LDL, low-density lipoprotein; LV, left ventricular; PCI, percutaneous coronary intervention; SHR, stress hyperglycaemia ratio; SMuRFs, standard modifiable cardiovascular risk factors; STEMI, ST-elevation myocardial infarction.

All estimates compare patients without a documented SMuRF with those with ≥1 SMuRF and are adjusted for age (except the model for age) and sex.

a Analytic cohort of 1494 patients.

b Difference in means; the adjusted difference in medians was −0.03 (−0.13 to 0.06; p = 0.473)—see Supplementary Table S3. The in-hospital death model uses Firth penalised logistic regression additionally adjusted for STEMI presentation, with profile penalised-likelihood CIs (53 events). Estimates after exclusion of recording-bound values are given in Supplementary Table S1. Abbreviations as in Table 3.

Figure 4-

Distribution of the SHR. (A) Distribution in the analytic cohort; the dotted line marks an SHR of 1.0 and the dashed lines the tertile boundaries. (B) SHR by SMuRF status (violin plots with box plots); the medians are similar (p = 0.731) but the variances differ (p < 0.001), so the means differ. (C) Cumulative distributions for the two groups, which cross close to the median: patients without a documented SMuRF are more likely to exceed an SHR of 1.0 and much less likely to have high values. SHR, stress hyperglycaemia ratio; SMuRFs, standard modifiable cardiovascular risk factors.

Table 5-

Characteristics of the analytic cohort by tertile of the SHR (n = 1494).

VariableTertile 1 (≤1.09) n = 509Tertile 2 (1.10–1.52) n = 492Tertile 3 (≥1.53) n = 493p
Age (years)60 (53–66)60 (52–67)61 (53–67)0.542
Male sex375 (73.7)366 (74.4)369 (74.8)0.912
BMI (kg/m2)24.5 (21.2–28.3)24.5 (21.3–28.3)24.5 (21.2–28.3)0.981
Systolic blood pressure (mmHg)140 (125–156)140 (124–155)141 (126–159)0.169
Registry glucose (mg/dL)154 (125–191)173 (145–245)310 (216–454)<0.001
HbA1c (%)8.2 (7.0–10.1)6.2 (5.6–8.2)6.6 (5.2–8.6)<0.001
SHR0.88 (0.73–0.99)1.30 (1.19–1.39)1.99 (1.71–2.45)<0.001
eGFR (mL/min/1.73 m2)78 (54–98)75 (54–98)78 (51–98)0.958
LDL cholesterol (mg/dL)120 (68–167)107 (71–153)117 (75–170)0.069
Hypertension356 (69.9)242 (49.2)347 (70.4)<0.001
Diabetes mellitus365 (71.7)262 (53.3)330 (66.9)<0.001
Dyslipidaemia290 (57.0)228 (46.3)297 (60.2)<0.001
Current smoking216 (42.4)173 (35.2)218 (44.2)0.009
No documented SMuRF36 (7.1)139 (28.3)29 (5.9)<0.001
Previous heart failure103 (20.2)69 (14.0)85 (17.2)0.034
STEMI presentation279 (54.8)277 (56.3)272 (55.2)0.886
Myocardial infarction (STEMI or NSTEMI)410 (80.6)401 (81.5)404 (81.9)0.845
GRACE risk score138 (101–178)127 (90–168)143 (98–175)0.005
Killip class III–IV112 (22.0)100 (20.3)107 (21.7)0.789
Killip class II–IV219 (43.0)187 (38.0)196 (39.8)0.258
LV ejection fraction (%)52 (48–56)52 (48–56)52 (48–56)0.410
LV ejection fraction <40%108 (21.2)105 (21.3)108 (21.9)0.961
Vessels treated, n2 (1–3)2 (1–3)2 (1–3)0.956
LAD treated342 (67.2)327 (66.5)340 (69.0)0.689
Multivessel PCI (≥2 vessels treated)330 (64.8)314 (63.8)325 (65.9)0.788
In-hospital all-cause death23 (4.5)11 (2.2)12 (2.4)0.067

[i] BMI, body mass index; eFGR, estimated glomerular filtration rate; IQR, interquartile range; LAD, left anterior descending artery; LDL, low-density lipoprotein; LV, left ventricular; NSTEMI, non-ST-elevation myocardial infarction; PCI, percutaneous coronary intervention; SHR, stress hyperglycaemia ratio; SMuRFs, standard modifiable cardiovascular risk factors; STEMI, ST-elevation myocardial infarction.

Figure 5-

SHR, markers of index-event severity and in-hospital death. (A) Event rates across SHR tertiles. (B) ORs per 1 SD increase in SHR: unadjusted, Model 1 and Model 2 (without the GRACE score) for each severity marker, and Firth-penalised unadjusted, Model 1, Model 2 (sensitivity) and GRACE-adjusted estimates for in-hospital death. (C) Area under the ROC curve with bootstrap 95% CIs for SHR and registry glucose; the GRACE score is shown only for in-hospital death, because Killip class is a component of the score. The dashed line marks chance discrimination. ORs, odds ratios; SD, standard deviation; SHR, stress hyperglycaemia ratio.

Table 6-

Association of the SHR with markers of index-event severity and in-hospital death (analytic cohort, n = 1494).

EndpointEvents/nModelOR per 1 SD of SHR (95% CI)p
Killip class III–IV319/1494Unadjusted1.01 (0.89–1.14)0.918
Model 1a1.01 (0.89–1.15)0.866
Model 2b1.02 (0.90–1.16)0.757
Model 2, boundary covariates excludedc1.01 (0.89–1.16)0.848
Killip class II–IV602/1494Unadjusted0.95 (0.85–1.05)0.295
Model 1a0.95 (0.85–1.05)0.317
Model 2b0.95 (0.85–1.06)0.370
Model 2, boundary covariates excludedc0.95 (0.85–1.06)0.379
LV ejection fraction <40%321/1494Unadjusted1.06 (0.94–1.19)0.341
Model 1a1.07 (0.95–1.20)0.292
Model 2b1.08 (0.96–1.23)0.208
Model 2, boundary covariates excludedc1.09 (0.96–1.24)0.199
In-hospital all-cause death46/1494Unadjusted (Firth)d0.73 (0.48–1.05)0.098
Model 1 (Firth)d0.71 (0.45–1.05)0.092
Model 2 (Firth), sensitivityd,e0.69 (0.44–1.02)0.062
GRACE-adjusted (Firth)d,f0.74 (0.49–1.07)0.114

CI, confidence interval; LV, left ventricular; OR, odds ratio; SD, standard deviation; SHR, stress hyperglycaemia ratio; VIF, variance inflation factor.

a Model 1: age, sex, STEMI presentation, diabetes mellitus and eGFR.

b Model 2: Model 1 plus hypertension, dyslipidaemia, current smoking, BMI, LDL cholesterol and previous heart failure. The GRACE score, included in the original Model 2, was removed because Killip class is one of its components. Maximum VIF 1.42.

c Records with LDL cholesterol, creatinine/eGFR or BMI at a recording bound excluded (n = 1314).

d Firth penalised logistic regression with profile penalised-likelihood CIs and penalised likelihood-ratio p values.

e About 3.8 events per estimated parameter; reported as a sensitivity analysis only, Model 1 being the primary adjusted mortality model.

f SHR adjusted for the GRACE score only. 1 SD of SHR = 0.76.

Table 6-

(continued). Tertile analysis of the same endpoints

EndpointModelTertile 1 (≤1.09)Tertile 2 (1.10–1.52)Tertile 3 (≥1.53)p for trend
Killip class III–IVModel 11 (reference)0.88 (0.65–1.20)0.97 (0.72–1.32)0.863
Model 21 (reference)0.94 (0.68–1.29)1.01 (0.74–1.37)0.975
Killip class II–IVModel 11 (reference)0.79 (0.61–1.02)0.87 (0.67–1.12)0.264
Model 21 (reference)0.84 (0.65–1.10)0.89 (0.68–1.15)0.355
LV ejection fraction <40%Model 11 (reference)0.98 (0.72–1.34)1.03 (0.76–1.40)0.835
Model 21 (reference)1.10 (0.80–1.51)1.08 (0.79–1.48)0.623
In-hospital all-cause death (Firth)Unadjusted1 (reference)0.49 (0.23–0.99)0.54 (0.26–1.06)0.055
Model 11 (reference)0.41 (0.19–0.83)0.50 (0.24–0.99)0.032
Model 2 (sensitivity)1 (reference)0.40 (0.18–0.84)0.48 (0.23–0.96)0.026

[i] OR, odds ratios

Table 7-

Chronic and acute glycaemic measures by documented SMuRF status (analytic cohort, n = 1494).

Glycaemic measure≥1 SMuRF (n = 1290)No documented SMuRF (n = 204)p
HbA1c (%)7.7 (6.1–9.5)5.9 (5.5–6.0)<0.001
Estimated average glucose (mg/dL)174 (128–226)123 (111–125)<0.001
Registry glucose (mg/dL)204 (151–310)150 (126–170)<0.001
SHR, median (IQR)1.30 (0.94–1.79)1.27 (1.13–1.43)0.731
SHR (mean)1.481.30see footnote
SHR, SD0.810.25<0.001a
SHR >1.0900/1290 (69.8)189/204 (92.6)<0.001
SHR >1.25676/1290 (52.4)108/204 (52.9)0.946
SHR >1.5475/1290 (36.8)37/204 (18.1)<0.001
SHR >2.0235/1290 (18.2)4/204 (2.0)<0.001

IQR, interquartile range; SD, standard deviation; SHR, stress hyperglycaemia ratio; SMuRF, standard modifiable cardiovascular risk factor. Median (IQR) or n/N (%).

a Levene test for equality of variances. Age- and sex-adjusted differences (no documented SMuRF minus ≥1 SMuRF): mean −0.17 (−0.28 to −0.06; p = 0.003); median −0.03 (−0.13 to 0.06; p = 0.473). The lower mean reflects the absence of a long right tail in patients without a documented SMuRF rather than a shift of the whole distribution (Supplementary Table S3).

Supplementary Table S1 -

Adjusted differences between patients without and with a documented SMuRF, with and without records at the recording bounds of each variable.

VariableAll records: difference (95% CI)nBoundary records excluded: difference (95% CI)n
LDL cholesterol (mg/dL)−38.25 (−47.55 to −28.94)1702−43.09 (−51.85 to −34.34)1604
Total cholesterol (mg/dL)−35.43 (−46.87 to −23.99)1702−40.02 (−50.84 to −29.20)1546
Creatinine (mg/dL)−0.38 (−0.67 to −0.10)1702−0.26 (−0.46 to −0.06)1636
eGFR (mL/min/1.73 m2)3.69 (−0.53 to 7.92)17023.15 (−0.90 to 7.19)1648
GRACE risk score−18.66 (−25.46 to −11.87)1702−19.97 (−26.60 to −13.34)1626
Heart rate (beats/min)−4.89 (−9.12 to −0.66)1702−5.56 (−9.57 to −1.54)1643
BMI (kg/m2)−1.55 (−2.39 to −0.70)1702−1.78 (−2.60 to −0.97)1669

[i] BMI, body mass index; CI, confidence interval; LDL, low-density lipoprotein; SMuRFs, standard modifiable cardiovascular risk factors. Linear regression adjusted for age and sex. In the right-hand columns, records at the lower or upper recording bound of that variable (Table 1) were excluded.

Supplementary Table S2 -

SHR analyses under four approaches to HbA1c values at the recording bounds.

ApproachnKillip III–IVKillip II–IVLVEF <40%In-hospital death (Firth)SHR difference, no documented SMuRF versus ≥1 SMuRF
Exclusion (primary)14941.01 (0.89–1.15)0.95 (0.85–1.05)1.07 (0.95–1.20)0.71 (0.45–1.05)−0.17 (−0.28 to −0.06)
Retention of recorded values17021.04 (0.93–1.16)0.96 (0.87–1.06)1.09 (0.98–1.21)0.80 (0.55–1.09)−0.25 (−0.36 to −0.13)
Multiple imputation (treated as missing)17021.03 (0.91–1.16)0.97 (0.87–1.07)1.06 (0.94–1.19)0.69 (0.47–1.03)−0.16 (−0.27 to −0.04)
Censored imputation17021.04 (0.94–1.15)0.96 (0.88–1.05)1.08 (0.98–1.19)0.85 (0.64–1.13)−0.31 (−0.44 to −0.18)

[i] BMI, body mass index; LDL, low-density lipoprotein; OR, odds ratio; SD, standard ratio; SHR, stress hyperglycaemia ratio; SMuRFs, standard modifiable cardiovascular risk factors; STEMI, ST-elevation myocardial infarction.

[ii] ORs per 0.76 units of SHR (1 SD in the analytic cohort), adjusted as in Model 1. The last column is the age- and sex-adjusted mean difference. Multiple imputation: HbA1c for the 208 boundary records imputed 20 times from a linear model (diabetes, registry glucose, age, sex, BMI, LDL cholesterol, hypertension, dyslipidaemia, current smoking, SMuRF status, STEMI) fitted in non-boundary records, with parameter uncertainty; censored imputation draws from the same model truncated to 3.0%–4.0% (lower bound) or 15.0%–20.0% (upper bound). Estimates combined by Rubin's rules (Wald intervals); the exclusion and retention mortality intervals are profile penalised-likelihood intervals.

Supplementary Table S3 -

Comparison of the SHR between patients without and with a documented SMuRF using different summary measures (analytic cohort, n = 1494)

Measure≥1 SMuRF (n = 1290)No documented SMuRF (n = 204)Difference (95% CI)
Median (IQR)1.30 (0.94–1.79)1.27 (1.13–1.43)Mann–Whitney p = 0.731
Mean (SD)1.48 (0.81)1.30 (0.25)Levene p < 0.001
Unadjusted mean difference−0.17 (−0.29 to −0.06); p = 0.002
Adjusted mean difference−0.17 (−0.28 to −0.06); p = 0.003
Adjusted difference in medians−0.03 (−0.13 to 0.06); p = 0.473
Adjusted ratio of geometric means0.98 (0.91–1.04); p = 0.489
Adjusted difference, 25th percentile0.18 (0.11–0.26); p < 0.001
Adjusted difference, 75th percentile−0.38 (−0.51 to −0.24); p < 0.001
Adjusted difference, 90th percentile−0.80 (−1.01 to −0.59); p < 0.001
Adjusted mean difference, SHR ≤2.0 only (n = 1255)0.10 (0.04–0.15); p < 0.001

[i] CI, confidence interval; IQR, interquartile range; SD, standard deviation; SHR, stress hyperglycaemia ratio; SMuRFs, standard modifiable cardiovascular risk factors.

[ii] Differences are no documented SMuRF minus ≥1 SMuRF, adjusted for age and sex (linear regression for means and log-transformed SHR; quantile regression for percentiles). The groups have similar medians; the lower mean in patients without a documented SMuRF results from fewer high values (lower 75th percentiles and 90th percentiles), while their lower quartile is higher.

DOI: https://doi.org/10.2478/rjc-2026-0033 | Journal eISSN: 2734-6382 | Journal ISSN: 1220-658X
Language: English
Published on: Nov 6, 2026
Published by: Romanian Society of Cardiology
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2026 Sahlan Abadi, Mohammad Saifur Rohman, Wella Karolina, published by Romanian Society of Cardiology
This work is licensed under the Creative Commons Attribution 4.0 License.