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Consensus Statements on Dyslipidemia in Indian Women
*Corresponding author: Jyotsna Maddury, Professor and Head (Retd.), Department of Cardiology, Nizam’s Institute of Medical Sciences, Hyderabad, Telangana, India. janaswamyjyotsna@gmail.com
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Received: ,
Accepted: ,
How to cite this article: Chhabra ST, Vipperla S, Rao S, Maddury J. Consensus Statements on Dyslipidemia in Indian Women. Indian J Cardiovasc Dis Women. 2025;10:252-67. doi: 10.25259/IJCDW_72_2025
Abstract
Dyslipidemia is a major, yet under-recognized, driver of atherosclerotic cardiovascular disease (ASCVD) in Indian women. This expert consensus provides India-specific guidance on early detection, risk stratification, and management of lipid disorders across the female life course. Seventy-five specialists from cardiology, endocrinology, lipidology, obstetrics–gynecology, and primary care participated in a modified Delphi process with three structured rounds. An agreement threshold of ≥80% was maintained to develop statements based on 20 key clinical questions and a comprehensive review of international and Indian evidence. The consensus emphasizes early and repeated lipid screening. All women should have at least one lipid profile between ages 20 and 39 years, with earlier and more frequent testing in those with a family history of premature ASCVD, suspected familial hypercholesterolemia, polycystic ovary syndrome, gestational diabetes, pre-eclampsia, premature menopause, or autoimmune disorders. Life-stage checkpoints such as pre-conception, 6–12 weeks postpartum, and at menopause are highlighted as critical opportunities for evaluation and intervention. The panel developed India-specific, life-stage-oriented risk assessment and management statements for women, emphasizing early lipid screening, recognition of female-specific risk enhancers, and practical treatment pathways. Management begins with lifestyle optimization and, when indicated, stepwise pharmacotherapy: Statins as first line (avoiding routine use in pregnancy and lactation), ezetimibe or fibrates as add-on therapy, and PCSK9 inhibitors or Inclisiran for very-high-risk cases not at target. Bile-acid sequestrants are identified as the safest drug option during pregnancy or breastfeeding. This statement integrates global best practice with India-specific risk profiles and care pathways. By embedding life-stage-oriented screening, female-specific risk enhancers, and risk stratification into routine care, it provides a practical roadmap for clinicians and public health programs to reduce the burden of ASCVD in Indian women.
Keywords
Cardiovascular risk
Consensus guidelines
Dyslipidemia
Indian women
Lipid screening
lipoprotein
Pregnancy
INTRODUCTION
Preamble
Despite significant advances in lipid management and cardiovascular prevention, women, particularly in low- and middle-income countries like India, remain underdiagnosed, undertreated, and underrepresented in lipid research.[1-4] Recent epidemiological studies indicate that up to 81.2% of Indian women have at least one lipid abnormality, with 52–67% exhibiting low high-density lipoprotein-cholesterol (HDL-C), 25–30% elevated low-density lipoprotein cholesterol (LDL-C), and over 30% elevated triglycerides – clearly demonstrating that this is not an academic concern but a widespread publichealth challenge.[5] Global data also report a high prevalence of low HDL-C (40–52%) and hypertriglyceridemia (~25%), further highlighting the burden among women worldwide.[6]
Existing global and national dyslipidemia guidelines, such as the American College of Cardiology/American Heart Association (ACC/AHA), the European Society of Cardiology/European Atherosclerosis Society, and the Canadian Cardiovascular Society, provide broad frameworks but seldom address the unique biological, hormonal, and sociocultural determinants of lipid disorders in Indian women.[7,8] However, women face a unique combination of common risk factors, along with gender-specific ones.[9,10] Table 1 summarizes the traditional and female-specific risk factors. The exploration of dyslipidemia in women warrants comprehensive attention within clinical practice.[9,10]
| Category | Risk factors |
|---|---|
| Traditional | Age, hypertension, diabetes mellitus, smoking, diet, obesity, sedentary lifestyle, and family history.[20] |
| Female-specific | Premature menopause, adverse pregnancy outcomes (preeclampsia, gestational diabetes, preterm delivery, stillbirth, and fetal growth restriction), PCOS, premature ovarian insufficiency, and hormonal therapy.[20] |
| Pregnancy-related ASCVD risk enhancers | Preterm delivery, stillbirth, fetal growth restriction, and elevated lipoprotein (a).[16-19] |
| Autoimmune/other | Rheumatoid arthritis, lupus, antiphospholipid syndrome, thyroid disorders, and chronic kidney disease.[20] |
| Psychosocial | Depression, anxiety, low socio-economic status, stress, and loneliness.[20] |
ASCVD: Atherosclerotic cardiovascular disease, PCOS: Polycystic ovary syndrome
Indian data show distinct patterns of atherogenic dyslipidemia,[11,12] earlier onset of metabolic risk,[13] and suboptimal awareness and treatment adherence[14,15] among women. Furthermore, female-specific factors including pregnancy-related complications,[16-19] premature menopause,[20] and polycystic ovary syndrome (PCOS) also contribute to an increased cardiovascular risk profile in women.[21] They are under-recognized in cardiovascular risk assessment.
Recognizing these persistent gaps, this consensus was developed through a structured expert panel to provide pragmatic, evidence-informed recommendations that reflect the realities of Indian clinical practice. This consensus aims to close the gender gap in dyslipidemia recognition, risk assessment, and management among Indian women. This consensus goes beyond traditional clinical recommendations.
It represents a paradigm shift toward preventive, life-course cardiovascular care for Indian women, a silent but essential revolution aimed at shifting healthcare from disease treatment to proactive health promotion.
Epidemiology of dyslipidemia in Indian women
Dyslipidemia is a major, modifiable determinant of atherosclerotic cardiovascular disease (ASCVD) in women. A systematic review and meta-analysis of 206 studies (98.5% cross-sectional) revealed global prevalences of 24.5%, 27.16%, 40.53%, and 21.03% for hypertriglyceridemia, hypercholesterolemia, low HDL-C, and high LDL-C, respectively.[6] Table 2 provides the representative prevalence data of lipid level abnormalities.[22]
| Study | Population | TC>200 mg/dL (%) |
LDL-C>130 mg/dL (%) | Low HDL-C (%) | TG>150 mg/dL (%) |
|---|---|---|---|---|---|
| Pandey et al., 2013[27] | Urban versus rural women | 27.7 versus 13.5 | – | – | – |
| Guptha et al., 2014[28] | Urban Indians | 24.9 | 15.1 | 52.8 | 32.9 |
| ICMR-INDIAB-17, 2024[5] | Multicenter, India | 81.2 (any dyslipidemia) | – | 67 | – |
HDL-C: High-density lipoprotein cholesterol, LDL-C: Low-density lipoprotein cholesterol, TG: Triglycerides, TC: Total cholesterol
Emerging mechanistic and biomarker insights
Recent research highlights that the pathophysiology of dyslipidemia in Indian women extends beyond conventional lipid fractions. Elevated lipoprotein(a), remnant cholesterol, and non-HDL-C contribute significantly to atherogenic burden and residual risk, even when LDL-C appears optimal.[23,24]
Race and ethnicity
Race and ethnicity are important determinants of dyslipidemia and cardiovascular risk. South Asians, including Indian women, exhibit a distinct lipid phenotype characterized by lower HDL-C, higher triglycerides, small dense LDL particles, and elevated lipoprotein(a) compared with Western populations. However, the SHARE study comparing multiple ethnic groups found that Asian Indians had higher LDL-C, lower HDL-C, and pro-inflammatory small dense dysfunctional high-density lipoprotein (HDL) particles than Europeans and Chinese, despite similar HDL-C concentrations.[22]
The Cardiology Society of India (CSI) and the Lipid Association of India (LAI), therefore, recommend their own risk-stratification algorithm until a dedicated Indian tool is validated.[25]
Life-stage biology amplifies these population risks.[26] Figure 1 provides the life-course lipid trajectory in women.

- Life-course lipid trajectory in women. A conceptual schema based on aggregated data from observational studies showing patterns of lipid changes (LDL-C, HDL-C, and TG) across key female life stages: pregnancy, postpartum, perimenopause, and menopause. (LDL-C: Low-density lipoprotein cholesterol, HDL-C: High-density lipoprotein cholesterol, TG: Triglycerides.)
Taken together, these data underscore the need for early and repeated screening of high-risk women and for India-specific risk assessment and management strategies to reduce the[27-29] heavy burden of dyslipidemia-related cardiovascular disease. Further large, nationally representative studies are needed to confirm these patterns across India’s diverse regions.
Unique female risk determinants
However, women face a unique combination of common risk factors, along with gender-specific ones [Table 3].[9,10,30,31] The exploration of dyslipidemia in women warrants comprehensive attention within clinical practice.[9,10,26]
| Risk enhancer | Magnitude of risk | Evidence |
|---|---|---|
| Early/late menarche | 8% ↑ risk of metabolic syndrome per year change[30,31] | Meta-analyses |
| Premature menopause (<45 year) | 1.5× ↑ IHD risk, 23% ↑ stroke[13] | Cohort studies |
| Pre-eclampsia | 4× ↑ CHD, stroke, mortality[18] | Meta-analysis |
| Gestational diabetes | 63% ↑ ASCVD risk[19] | US cohort |
| PCOS | ↑ TG, ↑ TC, ↓ HDL-C[21,32,33] | Indian prevalence 4–22% |
| Lipoprotein (a) elevation in pregnancy | ↑ risk of pre-eclampsia, low birth weight[16] | Prospective studies |
ASCVD: Atherosclerotic cardiovascular disease, CHD: Coronary heart disease, IHD: Ischemic heart disease, HDL-C: High-density lipoprotein cholesterol, LDL-C: Low-density lipoprotein cholesterol, PCOS: Polycystic ovary syndrome, TG: Triglycerides, TC: Total cholesterol
Numerous pregnancy-related complications have been identified as potential precursors to an elevated risk of ASCVD later in life.[17,32-34]
A Korean study documented a relationship between height and dyslipidemia, revealing that short stature is significantly inversely associated with dyslipidemia in both Korean adolescents and adults.[35] Among adolescents, this inverse relationship between height and dyslipidemia exhibited sex-related differences. Specifically, the risk of hypercholesterolemia, hypertriglyceridemia, and hyper-LDLcholesterolemia was linked to height in boys, whereas only hyper-LDL-cholesterolemia showed a significant association with height in girls. In adults, all four types of dyslipidemia were confirmed to be negatively impacted by short stature in both men and women.[35]
Autoimmune conditions such as rheumatoid arthritis, systemic lupus erythematosus, and antiphospholipid syndrome affect women far more often than men and significantly increase long-term cardiovascular risk. The chronic inflammation associated with these disorders alters lipid behavior; HDL-C levels usually decrease, triglycerides rise, and LDL particles become more susceptible to oxidation, all of which accelerate plaque formation in blood vessels.[20] These problems may worsen during disease flares or with corticosteroid therapy, which is why major guidelines classify women with autoimmune diseases as a higher-risk group.[36-39]
Because of this, it is essential to check lipid levels early, right at the time of diagnosis, and to repeat them more frequently, especially when the disease is active or steroid doses increase, so that dyslipidemia can be identified and treated promptly.
METHODOLOGY
Formation of an expert panel
To develop these recommendations, we assembled a group of 75 experienced clinicians from across India, including cardiologists, endocrinologists, lipid specialists, obstetricians–gynecologists, and primary care physicians. All had long-standing clinical practice and academic experience and were chosen to reflect a broad geographic and professional mix.
We used a modified Delphi process to build consensus. The group worked through three structured rounds of review and voting held over several months. In each round, panel members rated their level of agreement with draft statements. A statement was accepted once at least 80% of the members agreed to it. Points of disagreement were discussed and revised before the next round.
These formal steps, combined with a review of current evidence and responses to 20 key clinical questions, helped ensure that the final statements reflect both shared expert judgment and published data.
Questionnaire of 20 key clinical questions with pooled expert responses
A 20-item questionnaire [Supplementary File 1] was developed based on the literature gaps and clinical challenges identified during preparatory meetings. Each question addressed a critical aspect of dyslipidemia management in women, such as:
Optimal age and frequency of lipid screening,
Life-stage-specific changes (puberty, pregnancy, and menopause),
Management of familial hypercholesterolemia (FH),
Statin safety during pregnancy and lactation,
Preferred pharmacologic and lifestyle interventions.
The questionnaire was distributed electronically to all panelists and to a broader group of practicing clinicians nationwide. Responses were collated and analyzed for convergence and variation. Items with consistent agreement (>80%) were advanced to consensus statements.
Integration of answers into final statements
Each question’s pooled responses were cross-checked against current evidence and harmonized with the narrative literature review. The final consensus statements – encompassing screening, risk assessment, pharmacotherapy, and life-stage-specific recommendations – represent the intersection of published data and expert clinical insight, ensuring both scientific validity and practical applicability in the Indian context.
CONSENSUS STATEMENT
Screening and risk assessment
Conventional tools for predicting ASCVD risk, such as the pooled cohort equations (PCE), tend to underestimate risk among South Asians because they were excluded from the derivation cohort.[25] Consequently, these tools are not recommended for implementation in Indian subjects.
While the QRESEARCH cardiovascular risk algorithm (QRISK 3) score performs better than the pooled cohort equations (PCE) in risk assessment for Indians, the lack of a dedicated, population-derived risk calculator continues to limit precision.[25,40]
Indian urban surveys demonstrate that 25–30% of adult women have dyslipidemia, and up to 40% remain undiagnosed or untreated, underscoring the need for region-specific risk recalibration.[5,41] Moreover, artificial intelligence-based and polygenic risk-score models are now being validated through ICMR and Apollo-led initiatives (2024–2025) to enable individualized ASCVD prediction tailored to Indian women [Table 4].[42]
| Key consensus statement |
|---|
| Measure a lipid profile once between ages 20 and 39; repeat every 4–6 years or earlier if indicated. |
| Dyslipidemia during pregnancy should be recognized as a clinically relevant cardiovascular risk factor in India. Selective screening should be performed in high-risk women, with emphasis on preconception counseling. |
| For high-risk women (premature ASCVD family history or suspected FH), screen by puberty and follow more frequently. |
| When female-specific risk enhancers are present (e.g., PCOS, GDM, preeclampsia, and premature menopause), women should be considered at higher risk and managed more aggressively. |
| Schedule life-stage checkpoints: pre-conception, 6–12 weeks postpartum, and at menopause. |
| Postpartum lipid assessment is essential for identifying persistent risk and planning long-term prevention strategies. |
| Educate on lifetime ASCVD risk and the limits of pooled-cohort equations in South Asians. |
| ASCVD: Atherosclerotic cardiovascular disease, FH: Familial hypercholesterolemia, ACC: American College of Cardiology, AHA: American Heart Association, PCOS: Polycystic ovary syndrome, GDM: Gestational diabetes mellitus, EAS: European Atherosclerosis Society, PCOS: Polycystic ovary syndrome, GDM: Gestational diabetes mellitus |
Despite clear recommendations in the CSI’s 2023 guidelines to use non-fasting lipid profiles for routine screening and to begin lipid assessment at age 18 (or sooner in those with risk-enhancing family histories), actual compliance with these guidelines in clinical practice is still inadequate. CSI suggests a goal LDL-C <100 mg/dL and non-HDL-C <130 mg/dL in general or low-risk individuals, while emphasizing robust lifestyle modification as foundational therapy.
The CSI 2023 clinical practice guidelines and the LAI-2023 update provide general guidance on dyslipidemia in Indian patients; however, they do not fully address female-specific risk factors.[25,43] This consensus statement was therefore developed to fill that gap.[44]
Age to start routine lipid testing
Our consensus recommends that all Indian women have at least one lipid profile between the ages of 20 and 39 years, ideally in the early 20s, and that testing be repeated every 4–6 years, or sooner if abnormalities are detected [Table 5].
| Key consensus statement |
|---|
| Establish an early baseline in the 20 s for all women in India. |
| Repeat testing every 4–6 years if normal; sooner if abnormal results or added risk factors are present. |
| In FH/premature ASCVD families, the onset begins by puberty and is linked to pediatric screening cycles (9–11 and 17–21 years). |
| At menopausal transition, obtain a complete lipid profile and reassess global risk. |
| ASCVD: Atherosclerotic cardiovascular disease, FH: Familial hypercholesterolemia |
This Indian consensus is broadly in line with the 2019 ACC/AHA guideline on primary prevention of cardiovascular disease, which advises measuring major risk factors, including a lipid profile, starting at age 20 and at least every 4–6 years.[40,45]
By recommending an early, baseline lipid profile and structured re-testing at key reproductive and hormonal milestones, these statements aim to address the higher lifetime cardiovascular risk observed in Indian women.
Subclinical atherosclerosis in women – role of imaging and biomarkers
The early identification of subclinical atherosclerosis provides a critical opportunity for timely intervention in women, who often present with atypical symptoms and delayed cardiovascular risk recognition [Table 6].[24,46]
| Key consensus statement |
|---|
| Consider CIMT or CAC screening in intermediate-risk or postmenopausal women. |
| Add hs-CRP, ApoB, and Lp (a) testing to routine lipid profiles when feasible. |
| Encourage reporting of BAC on mammography as a cardiovascular risk clue. |
| Use combined imaging and biomarker evaluation for personalized prevention in Indian women. |
| hs-CRP: High-sensitivity C-reactive protein, ApoB: Apolipoprotein B, Lp (a): Lipoprotein (a), CIMT: Carotid Intima-Media Thickness, CAC: Coronary artery calcium, BAC: Breast arterial calcification |
Lipoprotein(a) (Lp[a]) remains a powerful and independent determinant of residual ASCVD risk, especially in South Asians.[47,48]
High-risk and life-stage scenarios
As described before, high-risk patients require early and high doses of statin to decrease the lifetime risk of Cardiovascular diseases (CVD) [Table 7 and Figure 2].[26] To support patient awareness and improve adherence, a public-friendly infographic summarizing key messages for women is included [Table 8 and Figure 3].
| Life stage | Recommended screening/follow-up | Key considerations |
|---|---|---|
| Preconception | Baseline fasting or non-fasting lipid profile; counsel on diet and weight optimization. | Identify familial dyslipidemia, PCOS, and metabolic syndrome. |
| Pregnancy | No routine testing unless FH or prior APOs; monitor if TG>300 mg/dL. | Avoid statins; bile-acid sequestrants can be used if essential. |
| Postpartum | Lipid profile at 6–12 weeks; annually for at least 3 years after APOs. | Reassess ASCVD risk; reinforce adherence to diet and exercise. |
| Lactation | Defer statins until breastfeeding stops; reintroduce therapy if indicated. | Counsel on resuming pharmacotherapy after lactation. |
| Perimenopause/menopause | Complete lipid panel; evaluate ASCVD risk; manage weight and blood pressure. | HRT only for symptom relief, short-term, low dose in low-risk women. |
| Early menopause (<40 years) | Annual lipid evaluation and lifestyle counseling. | Prioritize early pharmacologic intervention. |
PCOS: Polycystic ovary syndrome, APOs: Apolipoprotein B, TG: Triglycerides, ASCVD: Atherosclerotic cardiovascular disease, FH: Familial hypercholesterolemia, HRT: Hormone replacement therapy
| Key consensus statement |
|---|
| Reclassify risk upward for adverse pregnancy outcomes, including pre-eclampsia, gestational diabetes, gestational hypertension, preterm delivery, stillbirth, and fetal growth restriction. |
| Screen at diagnosis/onset and every 2–4 years thereafter. |
| After GDM or preeclampsia: check fasting lipids at 6–12 weeks postpartum and periodically lifelong. |
| Coordinate care among cardiology, endocrinology, obstetrics/gynecology, lipidologists, and primary care physicians. |
GDM: Gestational diabetes mellitus

- Clinical algorithm for dyslipidemia management in Indian women. This infographic presents a simplified, office-friendly clinical workflow for dyslipidemia screening, risk stratification, female-specific risk reclassification, treatment escalation, and life-stage-based follow-up for Indian women. (APOs: Adverse pregnancy outcomes, ASCVD: Atherosclerotic cardiovascular disease, FH: Familial hypercholesterolemia, PCOS: Polycystic ovary syndrome, TG: Triglycerides, LDL-C: Low-density lipoprotein cholesterol, Lp(a): Lipoprotein(a)).

- Women and heart health: Five things every woman should know. Infographic designed for patient education and community awareness to promote early lipid testing, identification of female-specific cardiovascular risk factors, lifestyle modification, and timely follow-up across the life course. (PCOS: Polycystic ovary syndrome.)
Quantitative lipid targets and outcome metric
Lipid-management goals should be individualized according to the cardiovascular risk category. Given the high cardiometabolic burden and smaller body habitus of Indian women, slightly lower LDL-C and non-HDL-C thresholds are reasonable. The suggested targets for clinical practice are mentioned in Tables 9 and 10.
| Key consensus statement |
|---|
| Adolescence/early adulthood: baseline profile; earlier if strong family history or suspected FH. |
| Routine lipid testing to be done preconception or 6–12 weeks postpartum, and monitor closely after adverse outcomes. Lipid profile may be considered once pregnancy is diagnosed, to unmask any unknown cases of familial dyslipidemia. Monitor lipid profile in each trimester in patients with familial hypercholesterolemia and adverse pregnancy outcomes. |
| Lactation: avoid statins; consider bile-acid sequestrants for severe hypercholesterolemia. |
| Perimenopause/menopause: repeat complete profile; anticipate LDL-C/TG rise; and intensify risk reduction. |
| In postmenopausal women, comprehensive cardiovascular risk assessment – including complete lipid profiling, blood pressure, and diabetes evaluation – should guide individualized management aimed at achieving LDL-C <70 mg/dL (or<55 mg/dL in very-high-risk cases), emphasizing lifestyle modification, selective use of hormone therapy in low-risk women, and avoidance in those with established CVD. |
FDA: Food and Drug Administration, FH: Familial hypercholesterolemia, LDL-C: Low-density lipoprotein, TG: Triglyceride
| Risk category | LDL-C goal (mg/dL) | Non–HDL-C goal (mg/dL) | Comments/typical scenarios |
|---|---|---|---|
| Low–moderate risk | <100 | <130 | Primary prevention in women without major risk enhancers |
| High risk | <70 | <100 | Diabetes, CKD, autoimmune disease, PCOS, or ≥2 risk enhancers |
| Very high risk | <55 | <85 | Established ASCVD or familial dyslipidemia |
LDL-C: Low-density lipoprotein cholesterol, HDL-C: High-density lipoprotein cholesterol,CKD: Chronic kidney disease, PCOS: Polycystic ovary syndrome, ASCVD: Atherosclerotic cardiovascular disease
HDL-C >50 mg/dL and triglycerides <150 mg/dL remain desirable secondary targets.
Process and outcome metrics for implementation should include:
Percentage of high-risk women achieving LDL-C goal within 6 months of therapy
Statin adherence and persistence at 12 months
Proportion of postpartum and menopausal women screened annually.
Regular audits of these indicators within hospital- and community-based lipid programs can help monitor the real-world effectiveness and equity of cardiovascular prevention in women.[49-56]
Management
Lifestyle and behavioral interventions
Lifestyle modification, which includes dietary advice and exercise, remains the cornerstone of dyslipidemia treatment, regardless of age or gender [Table 10].[22,57]
Nutraceutical and mind–body approaches
In addition to standard lifestyle measures, several culturally relevant strategies can complement lipid management in Indian women. Diets emphasizing traditional grains (millets, barley, and sorghum), legumes, cold-pressed oils, nuts, and fermented foods improve lipid quality and glycemic stability.[58]
Nutraceuticals such as red yeast rice extract, omega-3 fatty acids, garlic, berberine, and plant sterols have shown modest reductions in LDL-C and triglycerides. They can be considered when cost or intolerance limit pharmacotherapy.[59,60]
Integrating yoga, pranayama, and mindfulness-based stress reduction improves lipid profiles, endothelial function, and adherence by lowering sympathetic tone and psychological stress [Table 11].[61-63]
| Key Consensus statement |
|---|
| Adopt a Mediterranean-style eating pattern; limit saturated fat and refined sugars. |
| Omega-3 supplementation in postmenopausal women resulted in a significant reduction in triglyceride levels and a modest increase in HDL and LDL. |
| Engage in ≥150 min/week moderate aerobic activity plus muscle-strengthening 2 days/week. |
| Target weight reduction if overweight/obese; support smoking cessation and sleep hygiene. |
| Provide culturally tailored counseling during pregnancy and postpartum. |
| Women-specific myths, caregiving roles, and socioeconomic factors reduce adherence to lipid therapy and lifestyle change; structured counseling and stress-reduction strategies, including yoga and mindfulness, improve continuity of care. |
| Incorporate traditional Indian diets, nutraceuticals, and yoga-based stress-management as culturally appropriate adjuncts to lipid-lowering therapy, improving adherence and overall cardiometabolic health. |
HDL: High-density lipoprotein, LDL: Low-density lipoprotein, CVD: Cardiovascular diseases
Pharmacological management
Statins
Over the past two decades, multiple randomized controlled trials have investigated the efficacy of 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) in lowering cholesterol levels among patients with a history of CHD or at high risk.[64-66]
Among statins, pravastatin, a hydrophilic agent, has not been associated with fetal malformations. Notably, a recent study conducted among patients with preeclampsia found no significant increase in drug side effects, congenital anomalies, or other adverse events related to pravastatin use.[29]
In summary, while statins offer substantial cardiovascular risk reduction, further research is needed to elucidate any potential gender-specific effects. Clinicians should consider individual patient characteristics and tailor treatment strategies accordingly. Statins are generally avoided in pregnancy. They can be restarted after breastfeeding ends; in rare, very-high-risk cases, they may be continued under specialist care.
According to the guidelines, ezetimibe and niacin should be discontinued at least 4 weeks before stopping contraception for women with FH who are planning to conceive. These medications should not be used during pregnancy or lactation.[29]
Fibrates, although also classified as Class C, may be considered later in pregnancy following a risk-benefit analysis. The AHA recommends considering fenofibrate or gemfibrozil in the second trimester if triglyceride levels exceed 500 mg/dL, even after implementing lifestyle modifications.[29] The AHA, in conjunction with the American College of Obstetricians and Gynecologists, advises that pregnant patients with FH and a history of pancreatitis may benefit from fenofibrate when triglyceride levels exceed 1000 mg/dL.[66-69]
Proprotein convertase subtilisin/kexin type 9 inhibitors
When LDL-C or ApoB targets are not achieved with maximally tolerated statin therapy, combination therapy is recommended. Adding ezetimibe provides an incremental LDL-C reduction of 18–25%, while PCSK9 inhibitors (alirocumab and evolocumab) can achieve reductions up to 60%. The combination of statin plus ezetimibe or PCSK9 inhibitor has shown superior cardiovascular risk reduction compared to statin monotherapy, especially in high- and very-high-risk women who often exhibit residual atherogenic burden despite adherence to therapy [Table 12].[69-78]
| Pharmacological agent | Key consensus statement |
|---|---|
| Statins | Statins are first-line for primary/secondary prevention outside pregnancy and lactation. |
| Use hydrophilic agents or alternate dosing in statin-associated symptoms; confirm adherence before switching. | |
| Discuss pregnancy plans; pause statins during pregnancy and breastfeeding unless in exceptional, very-high-risk cases. | |
| Escalate therapy if LDL-C/non-HDL-C remains above targets after adherence-optimized statin therapy. | |
| Consider alternate-day or low-dose statin therapy or switching to an alternative statin in women who develop symptoms of myalgia. If multiple statin regimens are not tolerated, non-statin therapies (Ezetimibe, PCSK9 inhibitors, and bempedoic acid) can be added or used alone to achieve the cholesterol goal. | |
| Ezetimibe | Add if LDL-C remains above target on maximally tolerated statin. |
| Add to intensive high-dose statin therapy in patients with ACS or those undergoing revascularization. | |
| Fibrates | Consider (prefer fenofibrate) when triglycerides ≥500 mg/dL to reduce the risk of pancreatitis. |
| Bile-acid sequestrants | Use when statins are contraindicated in pregnancy/lactation; monitor fat-soluble vitamins. |
| PCSK9 inhibitors and inclisiran | Use in very-high-risk patients not at LDL-C goal despite statin±ezetimibe. |
| Insufficient safety data in pregnancy—avoid during gestation and lactation. | |
| Inclisiran enables twice-yearly dosing; consider for adherence challenges outside pregnancy. | |
| CETP inhibitors (torcetrapib, dalcetrapib, and evacetrapib) | It may be considered as an add-on therapy in very-high-risk patients with persistently high LDL-C despite maximally tolerated statin+ezetimibe+PCSK9 inhibitors. |
| ApoA-I mimetics | They are not recommended for routine use; further evidence from long-term trials is awaited. |
FDA: Food and drug administration, CETP: Cholesteryl ester transfer protein, LDL-C: Low-density lipoprotein cholesterol, HDL-C: High-density lipoprotein cholesterol, PCSK9 inhibitors: Proprotein convertase subtilisin/kexin type 9 inhibitors, ACS: Acute Coronary Syndrome
Emerging HDL-targeted therapies
Several HDL-targeted approaches have been investigated, including cholesteryl ester transfer protein (CETP) inhibitors and ApoA-I mimetics.[78,79]
Bempedoic acid
For patients unable to tolerate statins, emerging evidence supports the efficacy of alternative lipid-lowering agents. LAI 2023 recommends adding a bile acid sequestrant or bempedoic acid if an additional 20% LDL-C reduction is required.[25,57]
Emerging triglyceride-lowering therapies
A notable recent advance in triglyceride-lowering therapy is the U.S. Food and Drug Administration approval of olezarsen in December 2024 for adults with familial chylomicronemia syndrome (FCS) as an adjunct to diet, marking the first approved agent for this rare condition.[80] However, it is not indicated for broader hypertriglyceridemia management outside FCS at present, and clinicians should not extrapolate its use to general dyslipidemia or common elevated-TG states until outcome data become available.[79]
Pharmacogenomic and individualized therapy
The response to lipid-lowering therapy varies considerably among Indian women due to genetic and metabolic diversity.[81] Pharmacogenomic studies have identified key gene variants such as CETP,[82] SLCO1B1,[82] and ANGPTL3,[12] which influence statin efficacy, myopathy risk, and triglyceride metabolism. Incorporating such information in clinical decision-making can optimize drug selection and dosing, reduce adverse effects, and improve adherence.
Advances in precision lipidology now include targeted therapies that modulate specific lipid pathways, such as ApoC-III and ANGPTL3 inhibitors[83] and RNA-based therapies[84] such as pelacarsen and olpasiran that lower lipoprotein(a) levels. These emerging treatments hold promise for high-risk women with familial or therapy-resistant dyslipidemia, particularly where traditional statins and ezetimibe provide suboptimal control.[22,78,85]
Other lipid-lowering drugs
Since 2021, a new, highly effective, and safe lipid-lowering drug, Inclisiran, has been available.[29] This drug uses the mechanisms of small-interfering RNA, allowing it to be administered only twice a year. According to data from the ORION-1 study, a single administration might be associated with an average reduction of 41% in LDL-C after nine months.[86,87]
Emerging therapies in dyslipidemia
Advances in molecular medicine are opening new frontiers for lipid management such as gene editing and lipid nanoparticles [Table 13].[78]
| Class | Example drugs | Key points in women | Pregnancy/lactation safety |
|---|---|---|---|
| Statins | Atorvastatin, rosuvastatin, and pravastatin | First-line, proven benefit; pravastatin is safer in intolerance[63-66] | Contraindicated except for very high risk[67] |
| Ezetimibe | – | Adjunct to statins[35] | Avoid in pregnancy[68] |
| Fibrates | Fenofibrate, and gemfibrozil | Useful in severe hypertriglyceridemia[29] | Consider only if TG >500–1000 mg/dL[29] |
| Bile acid sequestrants | Colesevelam | Modest LDL-C lowering, safe in pregnancy[29] | May↓ vitamin absorption[29] |
| PCSK9 inhibitors | Evolocumab, and alirocumab | Potent LDL-C lowering, equal efficacy in women[69] | Limited pregnancy data[69] |
| Inclisiran | – | Twice-yearly dosing, outcome data pending[70,71] | No safety data in pregnancy[71] |
| Apheresis | – | For HoFH, high Lp (a)[72] | Safe in specialized centers[72] |
LDL-C: Low-density lipoprotein cholesterol, HoFH: Homozygous familial hypercholesterolemia, Lp (a): Lipoprotein (a), PCSK9 inhibitors: Proprotein convertase subtilisin/kexin type 9 inhibitors, TG: Triglyceride
Implementation in Indian healthcare settings
The practical application of these consensus recommendations requires integration into routine clinical workflows across India’s diverse healthcare system, from large tertiary centers to primary and community clinics, which requires robust digital and public health integration [Table 14]. The panel identified several practical steps for implementation.
| Key consensus statements |
|---|
| Embed female-specific risk enhancers into EMRs/clinic templates. |
| Prompt lipid checks at life-stage transitions (pre-conception, postpartum, and menopause) |
| Track KPIs: screening rate (20–39 years), postpartum lipid testing after GDM/preeclampsia, statin adherence in high-risk women. |
| Provide multidisciplinary training and public health messaging tailored to women. |
| Overcoming healthcare inequity for rural, tribal, and low-income women, including low-cost non-fasting screening models. |
NPCDCS: National program for prevention and control of cancer, diabetes, cardiovascular diseases and stroke, NCD: Non-communicable disease, EHRs: Electronic health records; KPIs: Key Performance indicators; GDM: Gestational diabetes mellitus, EMRs: Electronic medical records
Alignment with national consensus and risk tools
The current national (CSI and LAI) consensus provides an evidence-based ASCVD risk assessment and lipid management algorithm tailored to Indian epidemiology and healthcare realities.[25] Our expert group has developed an India-specific consensus for life-stage-oriented screening and management of dyslipidemia in women. While existing tools, such as the LAI 2023 algorithm, have incorporated risk factors and female-specific enhancers (premature menopause, pregnancy complications, and PCOS), this consensus provides independent, focused recommendations to address gaps and offer practical guidance tailored to women [Figure 4].

- Risk-based lipid management algorithm incorporating female-specific risk enhancers. (PCOS: Polycystic ovary syndrome, FH: Familial hypercholesterolemia, PCSK 9: Proprotein convertase subtilisin/Kexin type 9).
Clinical workflow
At the primary care and obstetrics/gynecology interface, women should receive opportunistic lipid screening during routine reproductive health visits, antenatal care, postpartum checks, and perimenopausal consultations. Positive findings can then be triaged to higher levels of care using the risk categories (low, moderate, high, and very high). For example, a woman initially categorized as low risk but with a history of preeclampsia would be reclassified to at least moderate risk and offered more intensive monitoring and treatment.
Integration with electronic health records and registries
Embedding the recommendations in hospital and clinic electronic medical record systems, mobile health platforms, and community health worker tools can streamline risk calculation and follow-up reminders. Standardized templates should prompt clinicians to document life-stage data (pubertal age, pregnancy outcomes, and menopausal status) to capture risk enhancers.
Capacity building and awareness
Implementation will require training primary care physicians, obstetricians, and nurses in life-stage dyslipidemia and risk stratification. Public health messaging should encourage women to seek early baseline lipid checks and to understand the significance of female-specific risk factors.
Policy and programmatic integration
Inclusion of these recommendations in national noncommunicable disease (NCD) programs, workplace health schemes, and maternal-health initiatives will facilitate equitable access. Insurance and government health packages should support periodic lipid testing and evidence-based therapies for women across all socioeconomic strata.
Health-system integration and policy translation
Translating these consensus recommendations into national practice requires alignment with India’s ongoing public health frameworks, notably the National Program for Prevention and Control of Cancer, Diabetes, Cardiovascular Diseases, and Stroke and the Ayushman Bharat Health and Wellness Centers. Incorporating routine lipid screening and risk-factor assessment for women aged 40 and above into NCD clinics would strengthen early detection.
Integration with maternal and child-health programs can ensure postpartum lipid testing for women with gestational diabetes, pre-eclampsia, or preterm delivery. Electronic-medical-record prompts should capture female-specific risk enhancers (e.g., premature menopause, PCOS, and autoimmune disorders) to enable continuous risk tracking. Collaboration among cardiology, obstetrics, endocrinology, and primary-care teams, supported by government and professional societies, will be essential for scalable implementation and periodic audit. To evaluate performance and accountability, periodic audits may include the following key indicators: The proportion of women screened for dyslipidemia by age 40, the proportion of eligible women achieving LDL-C < 100 mg/dL (or <70 mg/dL in high-risk cases), and the median LDL-C reduction following initiation of therapy.
|
Pocket Consensus Statement: Top 10 Clinical Takeaways for Practitioners 1. Early screening: Every Indian woman should have at least one lipid profile between ages 20 and 39 years, with repeat testing every 4–6 years or earlier if risk factors are present. |
| 2. High-risk identification: Women with a family history of premature ASCVD, familial hypercholesterolemia, PCOS, premature menopause, or adverse pregnancy outcomes (GDM, preeclampsia, and preterm delivery) warrant early and more frequent screening. |
| 3. Life-stage checkpoints: Lipid testing should be prioritized pre-conception, 6–12 weeks postpartum, and at menopausal transition for timely risk reassessment. |
| 4. Female-specific risk enhancers: Conditions such as PCOS, autoimmune diseases, premature ovarian insufficiency, and adverse pregnancy outcomes should reclassify risk upward and trigger proactive management. |
| 5. Risk-based targets: LDL-C goals – <100 mg/dL (low/moderate risk), <70 mg/dL (high risk), and <55 mg/dL (very-high risk) – with non–HDL-C as secondary target (<130, <100, and <85 mg/dL, respectively). |
| 6. Lifestyle first: Emphasize traditional Indian diets, Mediterranean-style eating, yoga, physical activity (≥150 min/week), and weight control as the foundation of therapy. |
| 7. Pharmacotherapy: Statins remain first-line therapy outside pregnancy/lactation; ezetimibe, PCSK9 inhibitors, or bempedoic acid are add-ons if targets are unmet or intolerance exists. |
| 8. Pregnancy and lactation: Statins are contraindicated; bile-acid sequestrants are preferred when pharmacologic therapy is essential. |
| 9. Subclinical atherosclerosis: Use CIMT, CAC, Lipoprotein (a), Apolipoprotein B, and high-sensitivity C-reactive protein to refine risk stratification, especially in intermediate-risk or postmenopausal women. |
| 10. System implementation:Embed female-specific risk enhancers in EHRs, ensure multidisciplinary coordination, and audit key indicators – screening coverage, postpartum lipid checks, and statin adherence – to improve outcomes. |
In addition, community outreach and digital health models should be strengthened to improve continuity of care. This includes establishing tele-lipid clinics for remote counseling and medication follow-up and utilizing mobile health (mHealth) applications for adherence tracking, lifestyle reinforcement, and home-based lipid monitoring reminders. These models are beneficial for rural and semi-urban regions, where access to preventive cardiometabolic care remains limited.
CONCLUSION
Dyslipidemia is a major, yet preventable, contributor to cardiovascular morbidity and mortality in Indian women. Across life stages – from adolescence and reproductive years to menopause – unique hormonal transitions and female-specific risk enhancers such as PCOS, adverse pregnancy outcomes, and premature menopause interact with traditional risk factors to accelerate ASCVD.
This expert consensus provides India-specific, evidence-based statements on screening, risk assessment, and management, emphasizing early baseline lipid testing (for individuals aged 20–39 years), targeted high-risk screening from puberty, and repeat assessments at key reproductive and menopausal milestones. These recommendations, developed through expert consensus, provide precise risk stratification and management strategies tailored for Indian women across their life course.
Implementing these measures in routine clinical practice across primary care, obstetrics and gynecology, cardiology, and related fields of medicine offers a practical roadmap to reduce the lifelong burden of ASCVD in Indian women. By harmonizing global evidence with local epidemiology and expert clinical judgment, this consensus aims to shift the detection and treatment of dyslipidemia to earlier, more effective stages, ultimately improving cardiovascular health and survival among women in India.
Ethical approval:
Institutional Review Board approval is not required.
Declaration of patient consent:
Patient’s consent was not required as there are no patients in this study.
Conflicts of interest:
Dr. Shibba Takkar Chhabra, Dr. Sujatha Vipperla, Dr. Sarita Rao, and Dr. Jyotsna Maddury are on the Editorial Board of this journal.
Use of artificial intelligence (AI)-assisted technology for manuscript preparation:
The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.
Financial support and sponsorship: Nil.
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