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Original Article

A mitochondrial regulator protein, MNRR1, is elevated in the maternal blood of women with preeclampsia

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Article: 2297158 | Received 29 Jun 2023, Accepted 15 Dec 2023, Published online: 14 Jan 2024

Figures & data

Table 1. Demographics and clinical characteristics of the study population.

Table 2. Severity features of pregnant women with early and late preeclampsia.

Figure 1. Plasma MNRR1 concentrations in pregnant women with preeclampsia and controls. The median (IQR) plasma concentration of MNRR1 was significantly higher in patients with early [1632 (924–2926) pg/mL vs. 630 (448–4002) pg/mL; p = .03, adjusted p = .026] and late [1833 (1441–5534) pg/mL vs. 910 (526–6178) pg/mL; p = .001, adjusted p = .021] preeclampsia compared to uncomplicated pregnant women. Y-axis data are presented in logarithmic scale.

Figure 1. Plasma MNRR1 concentrations in pregnant women with preeclampsia and controls. The median (IQR) plasma concentration of MNRR1 was significantly higher in patients with early [1632 (924–2926) pg/mL vs. 630 (448–4002) pg/mL; p = .03, adjusted p = .026] and late [1833 (1441–5534) pg/mL vs. 910 (526–6178) pg/mL; p = .001, adjusted p = .021] preeclampsia compared to uncomplicated pregnant women. Y-axis data are presented in logarithmic scale.

Figure 2. Plasma MNRR1 concentrations in women with preeclampsia stratified by the presence of placental lesions of maternal vascular malperfusion (MVM) in early and late preeclampsia compared to their respective controls. For early preeclampsia, the patients with MVM lesions in the placenta had the highest median (IQR) plasma concentration of MNRR1 among the three groups [with MVM 2066 (1070–3188) pg/mL vs. without MVM 888 (812–1781) pg/mL, p = .03; and with MVM vs. controls 630 (448–4002) pg/mL, p = .018, adjusted p = .04]. By contrast, in late preeclampsia, patients with and those without MVM lesions in the placenta had a significantly higher median (IQR) plasma MNRR1 concentration than women in the control group [with MVM 1609 (1392–3135) pg/mL vs. controls 910 (526–6178), p = .1, adjusted p = .045; and without MVM 2023 (1578–8936) pg/mL vs. controls, p = .01]. Y-axis data are presented in logarithmic scale.

Figure 2. Plasma MNRR1 concentrations in women with preeclampsia stratified by the presence of placental lesions of maternal vascular malperfusion (MVM) in early and late preeclampsia compared to their respective controls. For early preeclampsia, the patients with MVM lesions in the placenta had the highest median (IQR) plasma concentration of MNRR1 among the three groups [with MVM 2066 (1070–3188) pg/mL vs. without MVM 888 (812–1781) pg/mL, p = .03; and with MVM vs. controls 630 (448–4002) pg/mL, p = .018, adjusted p = .04]. By contrast, in late preeclampsia, patients with and those without MVM lesions in the placenta had a significantly higher median (IQR) plasma MNRR1 concentration than women in the control group [with MVM 1609 (1392–3135) pg/mL vs. controls 910 (526–6178), p = .1, adjusted p = .045; and without MVM 2023 (1578–8936) pg/mL vs. controls, p = .01]. Y-axis data are presented in logarithmic scale.

Data availability statement

All data generated or analyzed during this study are included in this article. Further inquiries can be directed to the corresponding author at [email protected] (Dr. Romero).