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A Follow-up Study of Peripheral Neurological and Biochemical Involvement in Gestational and Overt Diabetes Mellitus
Akriti Kapila Sharma1, Ashwini Mahadule1, Sunita Mittal1
1Department of Physiology, AIIMS, Rishikesh, Uttarakhand, India.
Insights
Hyperglycaemia in pregnancy, including gestational diabetes mellitus (GDM) and overt diabetes mellitus (ODM), can cause subclinical peripheral neuropathy. Monitoring metabolic and neurological health post-childbirth is crucial for managing GDM and ODM.
Area of Science:
- Obstetrics and Gynecology
- Neurology
- Endocrinology
Background:
- Hyperglycaemia in pregnancy (HIP), encompassing gestational diabetes mellitus (GDM) and overt diabetes mellitus (ODM), affects approximately 1 in 6 pregnancies globally.
- Pregnancy involves metabolic changes and placental endocrine activity, intensifying hyperglycaemia and oxidative stress, potentially leading to peripheral neuropathy.
Purpose of the Study:
- To investigate the neurological effects of GDM and ODM by detecting subclinical peripheral neuropathy using nerve conduction studies (NCS).
- To correlate neurological findings with biochemical parameters in pregnant women with GDM and ODM.
Main Methods:
- A follow-up study involving 39 pregnant women divided into control, GDM, and ODM groups.
- Nerve conduction studies (sural and ulnar nerves) and biochemical analyses (FPG, HbA1c, insulin, HOMA-IR, chromium, etc.) were performed at multiple gestational stages and postpartum.
Main Results:
- Diabetic pregnant groups exhibited significant alterations in nerve conduction, particularly in sensory latencies and amplitudes of sural and ulnar nerves compared to controls.
- Elevated FPG, HbA1c, insulin, and HOMA-IR confirmed insulin resistance and poor glycaemic control in GDM and ODM groups.
- Significantly lower serum chromium levels were observed in diabetic pregnant women (p = .001).
Conclusions:
- Ongoing metabolic and neurological monitoring for GDM and ODM patients post-childbirth is essential.
- Early screening and targeted interventions, including micronutrient supplementation and lifestyle changes, may prevent neuropathy progression and long-term complications.
Background:
'Hyperglycaemia in pregnancy' (HIP) is one of the most common antenatal complications, affecting about one in six pregnancies globally. HIP is sub-classified into two categories, namely 'gestational diabetes mellitus' (GDM) and 'overt diabetes mellitus' (ODM). Pregnancy is characterised by the accumulation of adipose tissue and a growing placenta, acting as endocrine organs, thus intensifying the hyperglycaemic environment and building up oxidative stress by dysregulation of metabolic pathways, instigating peripheral neuropathy.
Purpose:
Due to paucity in existing literature on neurological influences of GDM and ODM, this follow-up study was planned to detect subclinical peripheral neuropathy by nerve conduction studies (NCS) and its correlation with biochemical parameters among them.
Methods:
Thirty-nine pregnant women were divided into three groups: control, GDM and ODM. The NCS (sural and ulnar nerves) and biochemical parameters, that is, fasting plasma glucose (FPG), glycated haemoglobin (HbA1c), serum fasting insulin, homeostatic model assessment of insulin resistance (HOMA-IR), serum chromium, serum N-carboxy-methyl lysine, total cholesterol, low-density lipoprotein, triglycerides and high-density lipoprotein, were recorded during different stages of gestation, that is, 24-28 weeks (first visit), 32-38 weeks (second visit) and 6-12 weeks after parturition (third visit).
Results:
Nerve conduction studies reveal significant alterations in diabetic pregnant groups compared to control pregnant women, particularly in sensory latencies and amplitudes of the sural and ulnar nerves. Significant hyperglycaemia (FPG, HbA1c), hyperinsulinaemia, and elevated HOMA-IR in GDM and ODM groups confirm insulin resistance and poor glycaemic control during pregnancy and postpartum. Chromium levels were markedly lower in diabetics (p = .001).
Conclusion:
This study necessitates ongoing metabolic and neurological monitoring in GDM and ODM after childbirth. Early screening and focused interventions, including micronutrient supplementation and lifestyle modifications, may help avert progression to overt neuropathy and mitigate long-term complications.
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